Настройки

Укажите год
-

Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

Подробнее
-

Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

Подробнее

Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
Ведите корректный номера.
Ведите корректный номера.
Ведите корректный номера.
Ведите корректный номера.
Укажите год
Укажите год

Применить Всего найдено 3101. Отображено 100.
19-04-2012 дата публикации

Nmr reaction monitoring flow cell

Номер: US20120092013A1
Принадлежит: Bruker Biospin Corp

A monitoring cell, used to perform a measurement in an NMR spectrometer of a reaction fluid produced by a reaction vessel, has a body having inlet and outlet transport coaxial capillaries for transporting the reaction fluid between the body and the reaction vessel. Cooling lines are also positioned coaxially with the transport capillaries to transport cooling liquid between the body and the reaction vessel. The cell further has a hollow sample probe for insertion into the NMR spectrometer and a coupler section that removably connects the sample probe to the body so that the inlet transport capillary extends through the body into the interior of the sample probe and the outlet transport capillary is sealed to the sample probe to allow reaction fluid that enters the sample probe via the inlet transport capillary to exit the sample probe via the outlet transport capillary.

Подробнее
03-05-2012 дата публикации

In Vivo 1H Magnetic Resonance Spectroscopy For The Diagnosis Of Testicular Function And Disease

Номер: US20120108944A1
Принадлежит: UNIVERSITY OF CALIFORNIA

This invention relates to the use of 1 H magnetic resonance spectroscopy for the diagnosis of testicular function and disease.

Подробнее
01-11-2012 дата публикации

Msc-selmqc method for simultaneous mapping of polyunsaturated fatty acids, lactate and choline in high fat tissues

Номер: US20120274323A1
Автор: Qiuhong He
Принадлежит: University of Pittsburgh

Systems and methods employing spin editing techniques to improve magnetic resonance spectroscopy (MRS) and magnetic resonance spectroscopic imaging (MRSI) are discussed. Using these spin editing techniques, magnetic resonance signals of one or more unwanted chemicals (that is, chemicals whose signals are to be filtered out or suppressed) chemicals can be suppressed, so that the signal(s) of a first set of chemicals can be obtained without signals from the one or more unwanted chemicals. Information about and differences between the molecular topologies of the first set of chemicals and the one or more unwanted chemicals can be used to design a sequence that suppresses the one or more unwanted chemicals while allowing acquisition of signal(s) from the first set of chemicals.

Подробнее
15-11-2012 дата публикации

Snmr pulse sequence phase cycling

Номер: US20120286779A1
Принадлежит: VISTA CLARA Inc

Technologies applicable to SNMR pulse sequence phase cycling are disclosed, including SNMR acquisition apparatus and methods, SNMR processing apparatus and methods, and combinations thereof. SNMR acquisition may include transmitting two or more SNMR pulse sequences and applying a phase shift to a pulse in at least one of the pulse sequences, according to any of a variety of phase cycling techniques. SNMR processing may include combining SNMR from a plurality of pulse sequences comprising pulses of different phases, so that desired signals are preserved and undesired signals are canceled.

Подробнее
13-12-2012 дата публикации

Nmr device for detection of analytes

Номер: US20120313639A1
Автор: W. David Lee
Принадлежит: T2 Biosystems Inc

This invention relates generally to detection devices having one or more small wells each surrounded by, or in close proximity to, an NMR micro coil, each well containing a liquid sample with magnetic nanoparticles that self-assemble or disperse in the presence of a target analyte, thereby altering the measured NMR properties of the liquid sample. The device may be used, for example, as a portable unit for point of care diagnosis and/or field use, or the device may be implanted for continuous or intermittent monitoring of one or more biological species of interest in a patient.

Подробнее
24-01-2013 дата публикации

Fourier Tickling For Homonuclear Decoupling in NMR

Номер: US20130021031A1
Принадлежит: Individual

A method for high resolution NMR (=nuclear magnetic resonance) measurements using the application of excitation pulses and the acquisition of data points, whereby a dwell time Δt separates the acquisition of two consecutive data points, which is characterized in that one or more tickling rf (=radio frequency) pulses of duration τ p are applied within each dwell time Δt, and that the average rf field amplitude of each of the tickling rf pulses approximately fulfills the condition ω 1 =ω 1 τ p /Δt=πJ wherein J is the scalar J-coupling constant and ω 1 =γB 1 with γ being the gyromagnetic ratio and B 1 being the strength of the magnetic component of each tickling rf pulse. This method is effective in decoupling homonuclear couplings.

Подробнее
21-03-2013 дата публикации

METHOD FOR THE COMPARATIVE ANALYSIS OF PROTEIN PREPARATIONS BY MEANS OF NUCLEAR MAGNETIC RESONANCE

Номер: US20130069646A1
Принадлежит: NMRTEC

The invention relates to a method for the comparative analysis and control of the quality of a protein preparation by means of nuclear magnetic resonance (NMR) spectrometry. This method can be used to compare three-dimensional protein conformations in different protein preparations without requiring the samples to undergo any particular preparation. In particular, the method can be used to determine if a selected protein is in the same three-dimensional conformation in different protein preparations, if it is degraded in the formulation or if it is interacting with some of the excipients present. Specifically, the method can be used for the analysis and control of the quality of therapeutic compounds, particularly biodrugs or biosimilars, in different samples, without altering said samples. 1. Method for the comparative analysis and the quality control of therapeutic compositions , implementing nuclear magnetic resonance (NMR) spectrometry , characterized in that it consists of the following steps:a) to select at least two different proteinic preparations containing a biodrug;b) to establish the spectral signature of the biodrug in the first proteinic preparation from at least two spectra of nuclear magnetic resonance;c) to establish the spectral signature of the biodrug in the second proteinic preparation from at least two spectra of nuclear magnetic resonance;d) to compare the spectral signatures of the biodrug in the first and in the second proteinic preparations;e) to determine from the spectral signatures obtained during steps b) and c) if the biodrug is identical in the first proteinic preparation and in the second proteinic preparation.2. Method of analysis according to claim 1 , characterized in that at least one nuclear magnetic resonance spectrum realized during step b) from one selected proteinic preparation implements a two-dimensional nuclear magnetic resonance method (2D NMR).3. Method of analysis according to claim 1 , characterized in that at least ...

Подробнее
18-04-2013 дата публикации

Nmr systems and methods for the rapid detection of analytes

Номер: US20130095494A1
Автор: Lori Anne Neely
Принадлежит: T2 Biosystems Inc

This invention features systems and methods for the detection of analytes, and their use in the treatment and diagnosis of disease.

Подробнее
09-05-2013 дата публикации

Measurement of Anaplerotic Flux by Hyperpolarization Transfer

Номер: US20130116547A1

Methods and composition for metabolic imaging are provided. For example, in certain aspects, methods for hyperpolarization transfer combined with hyperpolarization are provided. Furthermore, the invention provides methods for detecting magnetic resonance signals for biological processes such as anaplerosis.

Подробнее
23-05-2013 дата публикации

BIOLOGICAL DETECTOR AND METHOD

Номер: US20130127464A1
Принадлежит:

A biological detector includes a conduit for receiving a fluid containing one or more magnetic nanoparticle-labeled, biological objects to be detected and one or more permanent magnets or electromagnet for establishing a low magnetic field in which the conduit is disposed. A microcoil is disposed proximate the conduit for energization at a frequency that permits detection by NMR spectroscopy of whether the one or more magnetically-labeled biological objects is/are present in the fluid. 1. A method for detecting a target analyte in a sample , the method comprising:introducing magnetic particles comprising target-specific moieties to a sample comprising a target analyte under conditions such that particle/target analyte complexes are formed; andnon-optically detecting the target analyte in the sample.2. The method according to claim 1 , wherein the detecting step is accomplished in the presence of other components in the sample.3. The method according to claim 2 , wherein the non-optically detecting step comprises using a nuclear magnetic resonance (NMR) device.4. The method according to claim 3 , wherein the NMR device is used to measure a signal due to a change in relaxation rate.5. The method according to claim 4 , wherein the relaxation rate changes in the presence of the target analyte.6. The method of claims 5 , wherein said changes are selected from T1 claims 5 , T2 claims 5 , T2* claims 5 , or a combination thereof.7. The method according to claim 3 , wherein the NMR devices comprises:a magnet configured to produce a magnetic field;a vessel configured to hold the sample and being located within the magnetic field;a radio frequency (RF) coil located within the magnetic field.8. The method according to claim 7 , wherein the RF coil wraps around the vessel.9. The method according to claim 7 , wherein the magnetic is a permanent magnet.10. The method according to claim 1 , wherein the target-specific moieties are antibodies.11. The method according to claim 1 , ...

Подробнее
27-06-2013 дата публикации

METHOD FOR ANALYSIS OF THE CHEMICAL COMPOSITION OF THE HEAVY FRACTION OF PETROLEUM

Номер: US20130161502A1
Принадлежит: SCHLUMBERGER TECHNOLOGY CORPORATION

The chemical composition of petroleum samples is measured using orbitrap mass spectrometry with electrospray ionization (ESI). The orbitrap measurement is used in a screening to determine if one or more higher resolution (but more expensive) compositional analyses are justified. 1. A method of characterizing a petroleum sample that includes a heavy fraction having at least a plurality of polar compounds , comprising:a) ionizing the polar compounds in the petroleum sample; andb) measuring properties of the ionized polar compounds using an orbitrap mass spectrometer comprising an electrostatic ion trap mass analyzer that employs an outer barrel-like electrode and a coaxial inner spindle-like electrode that form an electric field with quadro-logarithmic distributions, the petroleum sample characterized, at least in part, by the measured properties.2. A method according to claim 1 , wherein the measured properties are related to heteroatom class distributions with respect to the petroleum sample.3. A method according to claim 2 , wherein the heteroatom class distributions correspond to a predetermined set of heteroatoms contained in the heavy fraction of the petroleum sample.4. A method according to claim 3 , wherein the predetermined set of heteroatoms consists of heteroatoms selected from the group consisting of nitrogen claim 3 , oxygen claim 3 , and sulphur.5. A method according to claim 3 , wherein the measured properties include an indication of the relative abundance of compounds that contain the predetermined set of heteroatoms.6. A method according to claim 1 , wherein the polar compounds are ionized using electrospray ionization (ESI).7. A method according to claim 6 , wherein ESI produces positively and negatively charged ions of the polar compounds claim 6 , and only properties of the negatively charged ions of the polar compounds are characterized using the orbitrap mass spectrometer.8. A method according to claim 6 , wherein ESI produces positively and ...

Подробнее
04-07-2013 дата публикации

BIOLOGICAL DETECTOR AND METHOD

Номер: US20130169276A1
Принадлежит: STC.UNM

A biological detector includes a conduit for receiving a fluid containing one or more magnetic nanoparticle-labeled, biological objects to be detected and one or more permanent magnets or electromagnet for establishing a low magnetic field in which the conduit is disposed. A microcoil is disposed proximate the conduit for energization at a frequency that permits detection by NMR spectroscopy of whether the one or more magnetically-labeled biological objects is/are present in the fluid. 1105-. (canceled)106. A biological detector comprising:a conduit for receiving a fluid containing one or more magnetically-labeled, biological objects to be detected;a magnetic field generator for establishing a magnetic field of about 0.5 to about 1.5 T in which the conduit is disposed; anda microcoil disposed proximate the conduit for energization at a frequency that permits detection by NMR of whether the one or more magnetically-labeled biological objects is/are present in the fluid.107. The biological detector of claim 106 , wherein the magnetic field generator comprises one or more permanent magnets.108. The biological detector of claim 107 , the biological detector comprising first and second permanent magnets having opposite poles spaced apart to form a gap in which said conduit is disposed.109. The biological detector of claim 106 , wherein the conduit comprises a capillary tube.110. The biological detector of claim 106 , wherein the conduit comprises an open-sided microchannel.111. The biological detector of claim 106 , wherein the microcoil comprises a solenoid-shaped coil disposed about the conduit.112. The biological detector of claim 106 , wherein the microcoil has an inner diameter of about 50 to about 550 microns.113. The biological detector of claim 112 , wherein the inner diameter is about 75 to about 125 microns.114. The biological detector of claim 113 , wherein the inner diameter is about 100 microns.115. The biological detector of claim 106 , wherein the ...

Подробнее
01-08-2013 дата публикации

PROBE FOR MAGNETIC RESONANCE FORCE MICROSCOPY AND METHOD THEREOF

Номер: US20130193970A1

A probe for use in Magnetic Resonance Force Microscopy (MRFM) to provide an image of a sample comprising: a magnetic field source adapted to orient the spin of the nuclei in a sample; a detector capable of detecting a magnetic field comprising an oscillator; at least one conductor substantially surrounding the oscillator for forming a RF antenna for transmitting a radio frequency electromagnetic field; whereby the at least one conductor transmits a radio frequency electromagnetic field that influences the nuclei in the sample, and whereby the detector detects how the nuclei are influenced through the oscillations of the oscillator to provide identification information concerning the content of the sample. Also included is a method for magnetic resonance force microscopy of a sample. 1. A probe for use in Magnetic Resonance Force Microscopy (MRFM) to provide an image or spectroscopy of a sample comprising:a magnetic field source adapted to orient the spin of the nuclei in a sample;a detector capable of detecting a magnetic field comprising an oscillator;at least one conductor substantially surrounding the oscillator for forming a RF antenna for transmitting a radio frequency electromagnetic field;whereby the at least one conductor transmits a radio frequency electromagnetic field that influences the nuclei in the sample, and whereby the detector detects how the nuclei are influenced through the oscillations of the longitudinal oscillator to provide identification information concerning the content of the sample.2. The probe of wherein the oscillator is a longitudinal oscillator; and wherein the magnetic field source is a magnetic field generator; and wherein the plurality of conductors comprise at least two coils mounted on a silicon substrate having a hole therein to provide the longitudinal oscillator access to a sample's surface; and wherein the at least two coils are adapted to be connected to an RF source; and wherein the longitudinal oscillator operates to ...

Подробнее
12-09-2013 дата публикации

METHOD AND SYSTEM FOR APPLYING NMR PULSE SEQUENCES WITH INTERACTING SHELLS

Номер: US20130234704A1
Принадлежит: SCHLUMBERGER TECHNOLOGY CORPORATION

A method and system for determining a nuclear magnetic resonance (NMR) property are described herein. The method includes applying a static magnetic field to a substance and applying an NMR pulse sequence to the substance. The NMR pulse sequence comprises a first pulse sequence segment applied at a first frequency to a shell and a second pulse sequence segment applied at a second frequency. The first pulse sequence segment generates a resonant signal in the shell and the second pulse sequence segment generates a characteristic within the resonant signal. The resonant signal is detected and an NMR property is determined using the characteristic within the detected resonant signal. 1. A method for determining a nuclear magnetic resonance (NMR) property , the method comprising:applying a static magnetic field to a substance; a first pulse sequence segment applied at a first set of frequencies to a shell; and', 'a second pulse sequence segment applied at a second set of frequencies, wherein the first pulse sequence segment generates a resonant signal in the shell and the second pulse sequence segment generates a characteristic within the resonant signal;, 'applying an NMR pulse sequence to the substance, wherein the NMR pulse sequence comprisesdetecting the resonant signal; anddetermining the NMR property using the characteristic within the detected resonant signal.2. The method according to claim 1 , wherein the second pulse sequence is applied before the first pulse sequence.3. The method according to claim 1 , wherein the second pulse sequence segment introduces an asymmetry in longitudinal magnetization within the shell.4. The method according to claim 1 , wherein the NMR property is a NMR property of the substance.5. The method according to claim 4 , wherein the NMR pulse sequence includes a waiting period between the first pulse sequence segment and the second pulse sequence segment.6. The method according to claim 5 , wherein the NMR property of the substance is ...

Подробнее
12-09-2013 дата публикации

Method and system for applying nmr pulse sequences using different frequencies

Номер: US20130234705A1
Принадлежит: Schlumberger Technology Corp

A method and system for applying nuclear magnetic resonance (NMR) sequences to a substance are described herein. The method includes applying an NMR pulse sequence to the substance using a non-resonant transmitter circuit. The NMR pulse sequence includes a first pulse sequence segment applied at a first frequency to a first shell within the substance and a second pulse sequence segment applied at a second frequency to a second shell. The second pulse sequence segment is initiated before the first shell reaches thermal equilibrium. In some cases, the first pulse sequence segment and the second pulse sequence segment are interposed within each other. Such NMR pulse sequences, with multiple pulse sequence segments, can also be applied to different atomic nuclei.

Подробнее
03-10-2013 дата публикации

PULSE SEQUENCE FOR HOMONUCLEAR J-DECOUPLING DURING NMR DATA ACQUISITION

Номер: US20130257425A1
Принадлежит:

A method is long observation based selective homonuclear decoupling includes acquiring one of CO or CA time domain signals during rotor synchronized breaks between decoupling pulses. 1acquiring one of CO or CA time domain signals during rotor synchronized breaks between decoupling pulses.. A method of long observation based selective homonuclear decoupling, comprising: This patent application claims priority from U.S. Provisional Patent Application 61/609,655 filed Mar. 12, 2012, which is hereby incorporated by reference.The invention relates to the field of nuclear magnetic resonance (NMR), and in particular to NMR data acquisition including a pulse sequence for homonuclear J-coupling.Many pulse sequences used in biological solid state NMR acquire either aliphatic carbons or carbonyl carbons. J-coupling between alpha carbons and carbonyl carbons in polypeptide chains can considerably broaden the resonances and lead to poorly resolved spectra in particular for large proteins.It is long known, that J-decoupling on carbons leads to increased resolution. Thus far J-decoupling was used in the indirect dimension or by acquiring 2 sub spectra, one in phase and the other in antiphase such that addition or subtraction of the sub spectra led to well resolved spectra; the technique is widely known as IPAP and commonly used in liquids NMR. Homonuclear decoupling on Ca or CO was used in Bertini's group about ten years ago and found technically too challenging compared to the easier to setup IPAP type experiments for Bertini's famous CaNCO, NCaCO and NCOCa experiments for 13C direct observe. In solid State NMR, the group of Professor Len Mueller developed similar J-driven homo- and heteronuclear correlation experiments based on Constant Time Uniform sign Cross peak COSY which came from the UC2QF COSY.An advantage of the CT experiment is J-decoupling in the indirect dimensions of the 2 and 3D experiments.However, there was the still considerable line broadening in the acquisition ...

Подробнее
10-10-2013 дата публикации

CONDUIT-CONTAINING DEVICES AND METHODS FOR ANALYTE PROCESSING AND DETECTION

Номер: US20130265054A1
Принадлежит: T2 Biosystems, Inc.

This invention features devices and methods for analyte processing and detection, and use of such methods, e.g., in the treatment and diagnosis of disease or determining the presence of a pathogen. 1216-. (canceled)217. A device comprising: (a1) a conduit inlet configured for introduction of a sample at a first site of said conduit; and', '(a2) a conduit outlet at a second site of said conduit;', 'said conduit being fluidically connected to:, '(a) a conduit comprising (b1) a slot for insertion of a cartridge comprising magnetic particles having binding moieties linked thereto, and', '(b2) a pin manifold fluidically connected to said conduit inlet and configured to be detachably attached to said cartridge, said pin manifold comprising a plurality of pins each capable of being fluidically connected to a sample of said cartridge;, '(b) a first unit comprising (c1) a plurality of zones comprising thermally conductive material, wherein the temperature of each said zone is maintained or modulated independently of said other zones;', '(c2) a second unit portion of said conduit for conducting flow of a sample through said zones, wherein said second unit portion of said conduit passes through each of said plurality of zones; and', '(c3) a thermal controller coupled to said plurality of zones, wherein said thermal controller is programmed to maintain or modulate said temperature of each said zone in a pre-defined manner;, '(c) a second unit fluidically connected to said first unit through said conduit and disposed downstream of said first unit, wherein said second unit is a sample processing unit that comprises (d1) a third unit portion of said conduit;', (d2.i) each said magnet is capable of being adjusted to create a magnetic field gradient inside said third unit portion of said conduit of sufficient strength to hold magnetic particles having binding moieties linked thereto in a particular volume in said third unit portion of said conduit proximal to said magnet;', '(d2.ii) ...

Подробнее
10-10-2013 дата публикации

LONGEVITY OF HYPERPOLARIZED ENHANCED SIGNALS FOR 'H NMR SPECTROSCOPY

Номер: US20130267036A1
Принадлежит:

A method and system for providing an article of manufacture with increased longevity of hyperpolarized H signals (and other species) for NMR spectroscopy and MRI. The method involves providing a material including a molecular species susceptible of NMR spectroscopy, by providing parahydrogen (and other appropriate species) to disperse within the material/solvent to establish increased longevity of the NMR signals. The material can be in a solution with a surfactant and catalysts added to enhance the persistence of parahydrogen (or other species) in the form of enhanced solubility, microbubbles or micelles and resultant hydrogenation (or other species) of the material. 1. A method of providing increased longevity of hyperpolarized H NMR signals for NMR spectroscopy and magnetic resonance imaging (MRI) , comprising the steps of:providing a material including a molecular species susceptible of NMR and MRI spectroscopy/imaging;providing parahydrogen for input to the material; andinputting the parahydrogen to the material by distributing parahydrogen through the material for a time to establish increased longevity of the NMR and MRI signals.2. The method as defined in further including the step of adding a surfactant to the material claim 1 , thereby providing increased persistence of the parahydrogen for the molecular species.3. The method as defined in further including the step of performing NMR spectroscopy or MRI on the material.4. The method as defined in further including the step of including an additive selected from the group of a catalyst claim 1 , material claim 1 , and a solvent.5. The method as defined in further including the step of adjusting parameters selected from the group of adjusting material and surfactant concentration claim 4 , adjusting solvent concentration and adjusting catalyst concentration.6. The method as defined in wherein the step of distributing is selected from the group of injection claim 1 , bubbling and adding appropriate ...

Подробнее
24-10-2013 дата публикации

Combined Spectroscopic Method for Rapid Differentiation of Biological Samples

Номер: US20130282300A1
Принадлежит:

A method for differentiating complex biological samples, each sample having one or more metabolite species. The method comprises producing a mass spectrum by subjecting the sample to a mass spectrometry analysis, the mass spectrum containing individual spectral peaks representative of the one or more metabolite species contained within the sample; subjecting the individual spectral peaks of the mass spectrum to a statistical pattern recognition analysis; identifying the one or more metabolite species contained within the sample by analyzing the individual spectral peaks of the mass spectrum; and assigning the sample into a defined sample class. 1. A method for differentiating complex biological samples , each sample having at least two metabolite species , comprising:producing a mass spectrum by subjecting a complex biological sample without using sample separation techniques to a mass spectrometry analysis, the mass spectrum containing individual spectral peaks representative of the at least two metabolite species contained within the sample;subjecting the individual spectral peaks of the mass spectrum to a statistical pattern recognition analysis;identifying at least two metabolite species across known metabolic pathways contained within the sample by analyzing the individual spectral peaks of the mass spectrum;correlating metabolite concentrations of at least two metabolite species across known metabolic pathways to identify specific changes in enzyme function; andassigning the complex biological sample into a defined sample class, thereby differentiating the complex biological sample.2. The method of claim 1 , wherein the sample comprises at least one of a biofluid claim 1 , tissue and cell.3. The method of claim 1 , wherein subjecting the sample to a mass spectrometry analysis comprises subjecting the sample to at least one of a desorption electro spray ionization analysis claim 1 , a direct analysis in real time (DART) procedure and an extractive electro spray ...

Подробнее
21-11-2013 дата публикации

Methods and Apparatus for Obtaining Enhanced Mass Spectrometric Data

Номер: US20130311110A1
Принадлежит: Thermo Fisher Scientific Bremen GmbH

A method comprising decomposing mass spectrometry data, especially of ion species that undergo multiple direction changes in a periodic manner, the data comprising signal and noise measured over time, into a sum of K harmonic component signals and a noise component, wherein the harmonic component signals and their number K are derived from the data and a determined quantity representative of the noise. The harmonic component signals and their number K may be determined iteratively on the basis of: using an initial value of K to calculate a minimised non-negative measure of difference R (K) between the measured and model data comprising data sets of K-harmonic component signals, and if R (K) does not lie within a noise range based on the quantity representative of the noise, changing the value of K and recalculating R (K) until R (K) lies within the noise range. Mass spectral information may be derived from the model data set.

Подробнее
05-12-2013 дата публикации

NMR QUANTIFICATION OF TMAO

Номер: US20130325353A1
Принадлежит:

A defined peak region residing between about 3.2 and 3.4 ppm of a proton NMR spectrum of an in vitro biosample is electronically evaluated to determine a level of trimethylamine-N-oxide (“TMAO”). The biosamples may be any suitable biosamples including human serum with a normal biologic range of between about 1-50 μM or urine with a normal biologic range of between about 0-1000 μM. 1. A method of determining a measure of TMAO in in vitro biosamples , comprising:electronically determining a level of trimethylamine-N-oxide (“TMAO”) of an in vitro biosample using a defined TMAO peak region having a single TMAO peak residing between about 3.2 and 3.4 ppm of a proton NMR spectrum.2. The method of claim 1 , further comprising:electronically identifying a pH-stable reference peak region in the NMR spectrum of the biosample;electronically identifying a defined calibration peak region in the NMR spectrum of the biosample, wherein the calibration peak region has a location that changes based on pH of the biosample; andelectronically calculating a distance between the reference and calibration peak regions; thenelectronically determining a location of the TMAO peak for the defined TMAO peak region based on the calculated distance.3. The method of claim 2 , wherein the electronically determining the TMAO peak region location is carried out using a defined relationship of location of the reference peak region to location of the calibration peak region.4. The method of claim 1 , wherein the biosample is a blood plasma or serum wherein the defined TMAO peak is at about 3.30 ppm.5. The method of claim 1 , further comprising:electronically identifying a defined calibration peak multiplet with peaks that can vary in distance apart from one another based on pH of the biosample;determining at least one distance between one or more of the peaks in the calibration peak multiplet; andelectronically determining a pH of the biosample based on the at least one determined distance;wherein the ...

Подробнее
12-12-2013 дата публикации

NMR MEASUREMENTS OF GLYCA

Номер: US20130328561A1
Принадлежит: LipoScience, Inc.

Biomarkers and/or risk assessments identify patients having an increased risk of certain clinical disease states including, for example, CHD, type 2 diabetes, dementia, or all-cause death (ACD) using NMR signal to measure a level of “GlycA” in arbitrary units or in defined units (e.g., μmol/L) that can be determined using a defined single peak region of proton NMR spectra. The GlycA measurement can be used as an inflammation biomarker for clinical disease states. The NMR signal for GlycA can include a fitting region of signal between about 2.080 ppm and 1.845 ppm of the proton NMR spectra. 1. A method of measuring GlycA , comprising:electronically obtaining a composite NMR spectrum of a fitting region of a biosample of a subject;electronically deconvolving the composite NMR spectrum using a defined deconvolution model with high density lipoprotein (HDL) components, low density lipoprotein (LDL) components, VLDL (very low density lipoprotein)/chylomicron components, and a plurality of curve fit functions associated with at least a GlycA peak region; andelectronically generating a measure of GlycA using the curve fit functions.2. The method of claim 1 , further comprising applying a conversion factor to the measure of GlycA to provide the measure in μmol/L.3. The method of claim 1 , wherein the curve fit functions are overlapping Lorentzian functions claim 1 , and wherein the measure of GlycA is generated by summing a defined number of Lorentzian functions.4. The method of claim 1 , wherein the deconvolution model further comprises a protein signal component for protein having a density greater than 1.21 g/L.6. The method of claim 1 , further comprising deconvolving another part of the NMR spectrum of the sample associated with a quartet of valine signals and generating an NMR measure of valine.7. The method of claim 5 , further comprising providing the valine and GlycA measurement in a test report.8. The method of claim 1 , wherein the plurality of curve fit ...

Подробнее
12-12-2013 дата публикации

MULTI-PARAMETER DIABETES RISK EVALUATIONS

Номер: US20130332082A1
Принадлежит:

Methods, systems and circuits evaluate a subject's risk of developing type 2 diabetes or developing or having prediabetes using at least one defined mathematical model of risk of progression that can stratify risk for patients having the same glucose measurement. The model may include NMR derived measurements of GlycA and a plurality of selected lipoprotein components of at least one biosample of the subject. 1. A method of evaluating a subject's risk of developing type 2 diabetes and/or of having prediabetes , comprising:programmatically calculating a diabetes risk index score of a subject using at least one defined mathematical model of risk of developing type 2 diabetes that includes at least one lipoprotein component, at least one branched chain amino acid and at least one inflammatory biomarker obtained from at least one in vitro biosample of the subject.2. The method of claim 1 , further comprising programmatically defining at least two different mathematical models of risk of developing type 2 diabetes claim 1 , the at least two different mathematical models including one for subjects on a statin therapy that includes lipoprotein component that are statin insensitive and one for subjects not on a statin therapy.3. The method of claim 1 , further comprising programmatically defining at least two different mathematical models of risk of developing type 2 diabetes claim 1 , the at least two different mathematical models with different lipoprotein components including one for fasting biosamples claim 1 , and one for non-fasting biosamples.4. The method of claim 1 , further comprising programmatically generating a report with a graph of risk of progression to type 2 diabetes in the future over a 1-7 year period versus ranges of fasting glucose levels and a quartile of risk associated with the diabetes risk index score.5. The method of claim 1 , wherein the graph shows references of at least first (low) and fourth (high) quartile DRI scores based on a defined ...

Подробнее
19-12-2013 дата публикации

METHOD FOR PREDICTING RESISTANCE TO HEAT DETERIORATION OF ISOPRENE RUBBER

Номер: US20130335078A1
Принадлежит: SUMITOMO RUBBER INDUSTRIES, LTD.

A method for predicting the resistance to heat deterioration of a sulfur-vulcanized isoprene rubber is disclosed. The nuclear magnetic resonance spectrum of the isoprene rubber is obtained by the use of a solid state nuclear magnetic resonance method employing magic angle spinning. The spectrum of a cross-linked structure α and the spectrum of a cross-linked structure β in the nuclear magnetic resonance spectrum are identified. The percentage of the cross-linked structure α and the percentage of the cross-linked structure β in the overall cross-linked structures of the sulfur are computed from the spectrum. From the computed percentages, the resistance to heat deterioration of the isoprene rubber is predicted. 1. A method for predicting resistance to heat deterioration of a sulfur-vulcanized isoprene rubber , comprising:measuring a nuclear magnetic resonance spectrum of the isoprene rubber by the use of a solid state nuclear magnetic resonance method employing magic angle spinning,identifying, in the nuclear magnetic resonance spectrum, a cross-linked structure α in which no double link exist near the reaction point of sulfur and a cross-linked structure β in which a double link exists near the reaction point of sulfur,obtaining, from the nuclear magnetic resonance spectrum, the ratio of the cross-linked structure α and the ratio of the cross-linked structure β to the overall cross-linked structures of sulfur, andpredicting the resistance to heat deterioration of the isoprene rubber, based on the obtained ratios.3. The method according to claim 1 , whereinthe rotation frequency in the magic angle spinning is in a range of from 16 to 17 kHz.4. The method according to claim 1 , wherein{'sup': 1', '1, 'said nuclear magnetic resonance spectrum is that of hydrogen nucleus (H) measured when the resonant frequency of hydrogen nucleus (H) is not less than 600 MHz.'}5. The method according to claim 1 , which isapplied to each of plural kinds of sulfur-vulcanized isoprene ...

Подробнее
09-01-2014 дата публикации

Snmr pulse sequencing methods and appratus

Номер: US20140009158A1
Принадлежит: VISTA CLARA Inc

Technologies applicable to SNMR pulse sequencing are disclosed, including SNMR acquisition apparatus and methods, SNMR processing apparatus and methods, and combinations thereof. SNMR acquisition may include transmitting SNMR pulse sequences according to any of a variety of techniques. SNMR processing may include combining SNMR from a plurality of pulse sequences.

Подробнее
16-01-2014 дата публикации

SYSTEM AND METHOD OF PERFORMING MAGNETIC RESONANCE SPECTROSCOPIC IMAGING

Номер: US20140015529A1
Принадлежит: THE JOHNS HOPKINS UNIVERSITY

A method of performing spatially localized magnetic resonance spectroscopy includes receiving a magnetic resonance image of an object; identifying a plurality C of compartments that generate magnetic resonance spectroscopy signals in the object including at least one compartment of interest; segmenting in at least one spatial dimension the magnetic resonance image of the object into the C compartments; acquiring magnetic resonance spectroscopy signals from the compartments by applying a plurality of M′ phase encodings applied in the at least one spatial dimension, wherein M′≧C; calculating a spatially localized magnetic resonance chemical shift spectrum from the at least one compartment of interest; and rendering a spatially localized magnetic resonance spectrum that is substantially equal to a spatial average of magnetic resonance chemical shift spectra from the at least one compartment of interest. A magnetic resonance spectroscopy and imaging system is configured to perform the above method. 1. A method of performing spatially localized magnetic resonance spectroscopy , comprising:receiving a magnetic resonance image of an object;identifying a plurality C of compartments that generate magnetic resonance spectroscopy signals in said object including at least one compartment of interest;segmenting in at least one spatial dimension said magnetic resonance image of said object into said C compartments;acquiring magnetic resonance spectroscopy signals from said compartments by applying a plurality of M′ phase encodings applied in the at least one spatial dimension, wherein M′≧C;calculating a spatially localized magnetic resonance chemical shift spectrum from the at least one compartment of interest; andrendering a spatially localized magnetic resonance spectrum that is substantially equal to a spatial average of magnetic resonance chemical shift spectra from the at least one compartment of interest.2. A method of performing spatially localized magnetic resonance ...

Подробнее
16-01-2014 дата публикации

Water relaxation-based sensors

Номер: US20140017816A1
Принадлежит: General Hospital Corp

This invention relates to magnetic resonance-based sensors and related methods.

Подробнее
06-02-2014 дата публикации

A microfluidic cell and a spin resonance device for use therewith

Номер: US20140035584A1
Принадлежит: Element Six Ltd

A microfluidic cell comprising: a microfluidic channel ( 32 ) for receiving a fluid sample; and a sensor ( 30 ) located adjacent the microfluidic channel; wherein the sensor comprises a diamond material comprising one or more quantum spin defects ( 34 ). In use, a fluid sample is loaded into the microfluidic cell and the fluid is analysed via magnetic resonance using the quantum spin defects.

Подробнее
06-03-2014 дата публикации

MAGNETIC RESONANCE SPECTROSCOPY PULSE SEQUENCE, ACQUISITION, AND PROCESSING SYSTEM AND METHOD

Номер: US20140064586A1
Принадлежит: NOCIMED, LLC

Systems and methods are provided for processing a set of multiple serially acquired magnetic resonance spectroscopy (MRS) free induction decay (FID) frames from a multi-frame MRS acquisition series from a region of interest (ROI) in a subject, and for providing a post-processed MRS spectrum. Processing parameters are dynamically varied while measuring results to determine the optimal post-processed results. Spectral regions opposite water from chemical regions of interest are evaluated and used in at least one processing operation. Frequency shift error is estimated via spectral correlation between free induction decay (FID) frames and a reference spectrum. Multiple groups of FID frames within the acquired set are identified to different phases corresponding with a phase step cycle of the acquisition. Baseline correction is also performed via rank order filter (ROF) estimate and a polynomial fit. Sections of the ROF may be excluded from the polynomial fit, such as for example sections determined to be associated with relevant spectral peaks. 1. A method for processing a set of multiple serially acquired magnetic resonance spectroscopy (MRS) free induction decay (FID) frames from a multi-frame MRS acquisition series from a region of interest (ROI) in a subject , and for providing a post-processed MRS spectrum , comprising:dynamically varying a parameter of a processing step between multiple parameter values affecting a corresponding change between multiple feature values of a feature of a processed result of performing the step on the set;performing the step on the set at each of the multiple parameter values and providing multiple processed results, respectively, comprising multiple respective feature values, respectively;comparing the feature values of the processed results;determining a chosen feature value among the multiple feature values based upon the comparison and corresponding to a chosen parameter value; andsetting the parameter to the chosen parameter ...

Подробнее
06-03-2014 дата публикации

SYSTEM AND METHOD FOR DETERMINING SIZE AND SIZE DISTRIBUTION OF MAGNETIC NANOPARTICLES USING VSM MAGNETIZATION DATA

Номер: US20140066751A1
Принадлежит: ARkival Technology Corp.

A method and apparatus for performing accurate measurements of the magnetic properties of magnetic nanoparticles (MNPs) in both liquid media and biological matrices for providing information on their size, size distribution and concentration in these media and matrices and, resulting in parameters that influence their functionality and effectiveness. 1. An apparatus for determining a size and size distribution of superparamagnetic nanoparticle cores in a sample , the apparatus comprising:a container to hold the sample;a magnetic measurement device configured to perform a magnetization analysis of the sample while in the container and generate magnetization data corresponding to the sample while in the container; and receive the magnetization data from the magnetic measurement device;', {'sub': H', 'H', 'H, 'perform a linear regression analysis of the magnetization data representing an asymptotic region in each of four branches (A, B, C, D) of a plotting of Mvs. 1/H, where Mis the measured magnetization in a magnetic field of intensity H approaching its saturation value and generate a first correlation curve of the form M=α/H+β;'}, {'sub': n', 'sat, 'calculate both a number average particle volume, {tilde over (V)}, and a saturation magnetization, M, of the sample, as a function of the first correlation curve;'}, {'sub': H', 'H, 'combine low field, linear data of Mfor branches A and C, and branches B and D, and obtain two plots of Mvs. H for values of H within a range from −50 Oe to +50 Oe;'}, {'sub': 'H', 'perform a linear regression analysis of the data in each branch and generate a second correlation curve of the form M=γH+δ;'}, {'sub': v', 'sat', 'H, 'calculate a volume average particle volume {tilde over (V)}as as a function of the saturation magnetization value Mobtained from the high field measurements, and using the value of the slope γ for the ratio of M/H;'}, {'sub': v', 'n', 'v', 'n, 'calculate a volume average spherical equivalent magnetic particle ...

Подробнее
10-04-2014 дата публикации

OPTICAL ANGULAR MOMENTUM INDUCED HYPERPOLARISATION IN INTERVENTIONAL APPLICATIONS

Номер: US20140097847A1
Принадлежит: KONINKLIJKE PHILIPS N.V.

A magnetic resonance spectroscopy assembly includes a magnet to generate a steady magnetic field, an RF transmit/receive antenna to transmit an RF excitation field into an examination region and acquire magnetic resonance signals from the examination region and a magnetic resonance spectrometer coupled to the RF transmit/receive antenna to collect magnetic resonance spectroscopy data from the magnetic resonance signals. An interventional instrument is provided with the assembly. The interventional instruments carries an optical module to generate photonic radiation endowed with orbital optical momentum (OAM). 1. A magnetic resonance spectroscopy assembly includinga magnet to generate a steady magnetic fieldan RF transmit/receive antenna to transmit an RF excitation field into an examination region and acquire magnetic resonance signals from the examination regiona magnetic resonance spectrometer coupled to the RF transmit/receive antenna to collect magnetic resonance spectroscopy data from the magnetic resonance signals andan interventional instrument carrying an optical module to generate photonic radiation endowed with orbital optical momentum (OAM).2. A magnetic resonance spectroscopy assembly as claimed in claim 1 , wherein the optical module combines the functions of (i) generation of photonic radiation endowed with orbital momentum and (ii) optical imaging of an field of view around the interventional instrument's distal end.3. A magnetic resonance spectroscopy assembly as claimed in claim 2 , wherein the optical module includes a rotatable reflector claim 2 , in particular a rotatable prism between an OAM-orientation and an imaging orientation claim 2 , the optical module generating OAM endowed photonic radiation with the prism in its OAM-orientation and the optical module imaging its field of view.4. A magnetic resonance spectroscopy assembly as claimed in claim 1 , wherein the magnet is integrated in the interventional instrument.5. A magnetic resonance ...

Подробнее
04-01-2018 дата публикации

PERFORMANCE HIGH VINYL BLOCK COPOLYMER COMPOSITIONS AND USES THEREOF

Номер: US20180002474A1
Принадлежит: KRATON POLYMERS U.S. LLC

Provided herein are improved performance high vinyl block copolymer compositions. The compositions may include a block copolymer and a polyolefin. The block copolymer may have a microstructure characterized by a vinyl content of equal to or greater than about 60%. The block copolymer may be a styrenic block copolymer. The polyolefin may include a polypropylene. Additional additives may be optionally added to the composition depending on the end-use application. The compositions may find utility in the preparation of various articles such as medical products including sterilized tubing, bags, and the like, films and injection molded articles. 1. A composition comprising i) a styrenic block copolymer present in an amount of from about 5 wt. % to about 95 wt. % based on the total weight of the composition and ii) a polyolefin present in an amount of from about 2 wt. % to about 98 wt. % based on the total weight of the composition wherein the composition has an Isotropic Ratio of less than about 1.4 as measured on extruded film with process temperature of less than about 250° C.2. The composition of wherein the styrenic block copolymer has the configuration (AB)X claim 1 , ABA claim 1 , (ABA)X claim 1 , (A-B) claim 1 , and (A-B-A) claim 1 , where A claim 1 , A claim 1 , and Aare polymer blocks of at least one monoalkenyl arene;n is equal to or greater than about 2;B is a polymer block of at least one conjugated diene; andX is a residue of a coupling agent.3. The composition of wherein the monoalkenyl arene is selected from the group consisting of styrene claim 2 , alpha-methylstyrene claim 2 , para-methylstyrene claim 2 , vinyl toluene claim 2 , vinylnaphthalene claim 2 , diphenyl ethylene claim 2 , para-butyl styrene claim 2 , and mixtures thereof.4. The composition of wherein X is a residue of an alkoxysilane coupling agent.5. The composition of wherein the styrene content of the A block ranges from about 8% to about 20% based on the weight percentage of polystyrene ...

Подробнее
05-01-2017 дата публикации

NMR Measurements of NMR Biomarker GlycA

Номер: US20170003269A1
Принадлежит: Liposcience Inc

Biomarkers and/or risk assessments identify patients having an increased risk of certain clinical disease states including, for example, CHD, type 2 diabetes, dementia, or all-cause death (ACD) using NMR signal to measure a level of “GlycA” in arbitrary units or in defined units (e.g., μmol/L) that can be determined using a defined single peak region of proton NMR spectra. The GlycA measurement can be used as an inflammation biomarker for clinical disease states . The NMR signal for GlycA can include a fitting region of signal between about 2.080 ppm and 1.845 ppm of the proton NMR spectra.

Подробнее
07-01-2016 дата публикации

METHODS AND APPARATUS FOR ANALYSIS OF SEALED CONTAINERS

Номер: US20160003753A1
Принадлежит:

This invention relates to methods and devices for NMR spectroscopy analyzing sealed containers e.g., food and beverage containers and other containers, and particularly according to specific embodiments sealed containers made of a conducting but generally nonferromagnetic metal or other conducting material. As discussed in above referenced applications, many current strategies for contaminant detection require a container to be violated, a process that can destroy the container or product and is impractical in large scale applications. The present invention overcomes these and other problems by providing methods and devices for the detection of contaminants and/or contraband in metal or conducting containers by NMR spectroscopy. 1. A method of analyzing one or more contents of one or more sealed containers , the method comprising:providing an NMR spectrometer and an NMR probe configured to accept a portion of the sealed container, all of the sealed container, or a portion or all of a plurality of sealed containers;positioning said portion of the sealed container, all of the sealed container, or a portion or all of a plurality of sealed containers within a data collection region of the NMR probe;establishing a homogeneous static magnetic field across the data collection region;applying an amplitude and frequency swept shaped RF pulse;collecting an NMR spectrum; andanalyzing the NMR spectrum, thereby analyzing one or more contents of the one or more sealed containers.2. The method of claim 1 , further wherein the RF pulse is a high powered pulse of at least 0.5 kW.3. The method of claim 1 , further wherein the shaped RF pulse is one or more of:a frequency and amplitude modulated adiabatic half soliton pulse;one or more adiabatic RF pulses;one or more adiabatic RF pulses in a mixture of pulses;a half soliton hyperbolic pulses;one or more linear and non-linear frequency and amplitude sweeps; andone or more mixtures of constant and variable amplitude and frequency ...

Подробнее
04-01-2018 дата публикации

Methods For Determining Plant Rubber Content With Low Field NMR

Номер: US20180003785A1
Принадлежит: BRIDGESTONE CORPORATION

Methods are described for quantifying an amount of natural rubber in a plant from a sample of the plant by obtaining a NMR spectrum and analyzing the signal peaks for the natural rubber in the plant sample and a standard component tested in combination with the plant sample. The NMR testing is conducted on a liquid state sample of a solution containing dissolved plant sample and standard component. A pre-determined and known amount of standard component is present in the liquid state sample and provides a reference for calculating an estimated amount of natural rubber in the plant sample. The estimated amount of natural rubber in the sample can be used to quantify the amount of extractable rubber in the sampled plant. 1. A method for quantifying an amount of natural rubber in a rubber-containing plant by use of low-field NMR , comprising the steps of:a. introducing a sample solution comprising a sample portion of the plant, a solvent and a known amount of standard rubber into a sample receiving space of a low-field NMR apparatus;b. obtaining a NMR spectrum of the sample solution, the NMR spectrum comprising a first signal peak corresponding to a single proton for the natural rubber present in the portion of the plant, the first signal peak having a first peak area, and a second signal peak corresponding to one or more protons for the standard rubber, the second signal peak having a second peak area;c. quantifying an amount of natural rubber in the portion of the plant by multiplying the first peak area by a conversion factor to obtain an estimate of the number of moles of natural rubber in the plant portion, the conversion factor being the number of moles of the standard rubber in the sample solution divided by the second peak area divided by the number of protons corresponding to the second signal peak.2. The method of claim 1 , further comprising the step of quantifying an amount of natural rubber in the sampled rubber-containing plant by dividing the quantified ...

Подробнее
01-01-2015 дата публикации

Nmr-based metabolite screening platform

Номер: US20150005243A1
Принадлежит: Childrens Medical Center Corp

Methods that enable one to specifically measure the metabolic product of a particular molecule in relatively few cells, e.g. primary cells, are described. The methods involve optionally preloading cells with labeled substrate (e.g. labeled by 13 C, 15 N, or 31 P). The methods allow for easy identification of metabolites that are differentially generated in cells of different phenotypes. The new methods for unbiased multi-dimensional NMR screening and rapid and efficient analysis of the NMR screening identify differentially expressed metabolites in different cell or tissue types. Analysis of the differentially expressed metabolites can present unique druggable targets to which small molecule therapeutics can be designed.

Подробнее
13-01-2022 дата публикации

METHODS TO PREDICT LIVER DISEASE MORTALITY USING LIPOPROTEIN LP-Z

Номер: US20220011388A1
Принадлежит:

Described herein are methods for the determination of patient mortality from alcoholic hepatitis in biosamples by NMR spectroscopy and more specifically for the determination of a Z index score based on lipoprotein constituent LP-Z in blood plasma and serum. 1. A method to predict patient mortality to alcoholic hepatitis comprising:acquiring an NMR spectrum of a biosample obtained from the subject;programmatically determining the concentration of LP-Z and total apoB-containing lipoproteins in the sample based on the NMR spectrum of the sample, wherein the NMR spectrum of the sample includes LP-X and LP-Z; andcalculating a Z index score.2. The method of claim 1 , wherein the acquiring step of the method comprises:producing a measured lipid signal lineshape for an NMR spectrum of the biosample obtained from a subject; andgenerating a calculated lineshape for the sample.3. The method of claim 2 , wherein the calculated lineshape is based on derived concentrations of lipoprotein components comprising LP-X and LP-Z.4. The method of claim 3 , wherein the derived concentration of each of the lipoprotein components is a function of a reference spectrum for that component and a calculated reference coefficient.5. The method of claim 2 , wherein generating step comprises calculating the reference coefficients for the calculated lineshape based on a linear least squares fit technique.6. The method of claim 2 , further comprising:determining that the degree of correlation between the initial calculated lineshape of the sample and a measured lineshape of the sample; anddetermining the presence of LP-Z based on the calculated lineshape if the degree of correlation between the calculated lineshape and the measured lineshape of the sample is above a predetermined threshold.7. The method of claim 1 , wherein the Z index score comprises a concentration of lipoprotein LP-Z claim 1 , LDL claim 1 , and VLDL.8. The method of claim 1 , wherein the Z index is a ratio of LP-Z concentration ...

Подробнее
02-01-2020 дата публикации

Multi-Parameter Diabetes Risk Evaluations

Номер: US20200005943A1
Принадлежит: LipoScience, Inc.

Methods, systems and circuits evaluate a subject's risk of developing type 2 diabetes or developing or having prediabetes using at least one defined mathematical model of risk of progression that can stratify risk for patients having the same glucose measurement. The model may include NMR derived measurements of GlycA and a plurality of selected lipoprotein components of at least one biosample of the subject. 1. A method of evaluating a subject's risk of developing type 2 diabetes and/or of having prediabetes , comprising:programmatically calculating a diabetes risk index score of a subject using at least one defined mathematical model of risk of developing type 2 diabetes that includes at least one lipoprotein component, at least one branched chain amino acid and at least one inflammatory biomarker obtained from at least one in vitro biosample of the subject.2. The method of claim 1 , further comprising programmatically defining at least two different mathematical models of risk of developing type 2 diabetes claim 1 , the at least two different mathematical models including one for subjects on a statin therapy that includes lipoprotein component that are statin insensitive and one for subjects not on a statin therapy.3. The method of claim 1 , further comprising pro grammatically defining at least two different mathematical models of risk of developing type 2 diabetes claim 1 , the at least two different mathematical models with different lipoprotein components including one for fasting biosamples claim 1 , and one for non-fasting biosamples.45-. (canceled)6. The method of claim 1 , wherein the at least one defined mathematical model of risk includes NMR derived measurements of a plurality of selected lipoprotein components of the at least one biosample of the subject claim 1 , and NMR measurements of at least one of GlycA and valine.7. The method of claim 1 , further comprising programmatically evaluating a fasting blood glucose measurement of the subject using at ...

Подробнее
08-01-2015 дата публикации

Nuclear magnetic resonance (nmr) spectroscopy device

Номер: US20150008922A1
Принадлежит: WAGENINGEN UNIVERSITEIT

The invention relates to a Nuclear Magnetic Resonance (NMR) spectroscopy device adapted for carrying out 1D and nD homo- and heteronuclear NMR spectroscopy measurements of a plurality of nuclei, comprising an RF coil adapted to transmit RF to and/or receive RF from a measuring volume, wherein the RF coil forms part of a non-tuned radiofrequency circuit. The invention further relates to a method of NMR data acquisition, a method of manufacturing a NMR spectroscopy device and a NMR-device holder.

Подробнее
08-01-2015 дата публикации

MAGNETIC RESONANCE IMAGING APPARATUS

Номер: US20150008925A1
Принадлежит:

There is provided a technique for obtaining temperature information for inside of a living body and accuracy information thereof in short time with low burden imposed on a subject. It is realized with a spectrum calculator configured to perform MRS or MRSI measurement for two kinds of substances showing difference of resonant frequencies and calculating spectra of magnetic resonance signals of the two kinds of substances, a temperature information calculator configured to calculate temperature information for inside of the subject on the basis of peaks of the calculated spectra, a temperature accuracy information calculator configured to calculate temperature accuracy information indicating accuracy of the temperature information on the basis of peaks of the calculated spectra, and a display information generator configured to generate display information to be displayed on a display device on the basis of the temperature information and the temperature accuracy information. 1. A magnetic resonance imaging apparatus comprising a static magnetic field generator configured to generate a static magnetic field in a space in which a subject is placed , a radio frequency magnetic field irradiator configured to irradiate a radio frequency magnetic field on the subject , a gradient magnetic field applicator configured to apply a gradient magnetic field to the subject , a detector configured to detect magnetic resonance signals generated from the subject , a scan controller configured to obtain magnetic resonance signals of two kinds of substances showing difference of resonant frequencies by controlling operations of the gradient magnetic field applicator , the radio frequency magnetic field irradiator , and the detector , an arithmetic unit configured to carry out operational processing of the magnetic resonance signals , and a display device configured to display information obtained by the operational processing , wherein:the arithmetic unit comprisesa spectrum ...

Подробнее
09-01-2020 дата публикации

METHOD AND SYSTEM FOR DETECTING AND IDENTIFYING ACUTE PAIN, ITS TRANSITION TO CHRONIC PAIN, AND MONITORING SUBSEQUENT THERAPY

Номер: US20200008741A1
Автор: Mountford Carolyn

The present invention relates to an MRS 1D or 2D method and system for obtaining spectral data of the brain of a subject and using neurochemical markers to enable whether a subject is experiencing acute pain, and providing the capacity to monitor response to therapy on an individual basis. The markers can be an increase of Fuc II, III, IV, VII and lactate. 1. A method for enabling detection of whether a subject is experiencing acute pain , comprising:obtaining magnetic resonance spectra from a subject's brain tissue using a magnetic resonance spectroscopy device; andproducing, from the magnetic resonance spectra obtained, spectral data which enables the detection of whether the subject is experiencing acute pain by detecting the presence of at least one neurochemical marker, by evaluating the data either by conventional methods or by data mining creating a classifier.2. The method of claim 1 , wherein the acute pain which can be detected is lower back pain.3. The method of claim 1 , wherein the magnetic resonance spectra is obtained using either a 1D MRS or 2D COSY.4. The method of claim 1 , wherein the neurochemical marker is Fuc II claim 1 , III claim 1 , IV and Fuc VII and lactate claim 1 , and wherein an increase of Fuc II claim 1 , III claim 1 , IV and Fuc VII and lactate in the spectral data enables the detection of whether the subject is experiencing acute pain.5. The method of claim 1 , wherein the neurochemical marker is Fuc II claim 1 , III claim 1 , IV and Fuc VII in the spectral data enables the detection of whether the subject is experiencing acute pain.6. The method of claim 1 , wherein the neurochemical marker is Fuc II claim 1 , III claim 1 , IV and Fuc VII claim 1 , lactate claim 1 , and wherein an increase of Fuc II claim 1 , III claim 1 , IV and Fuc VII and lactate in the spectral data claim 1 , enables the detection of whether the subject is experiencing acute pain.7. The method of claim 1 , including the step of treating the patient with a ...

Подробнее
11-01-2018 дата публикации

LOW BY-PRODUCT CONTENT POLYPHENYLENE POLYMETHYLENE POLYISOCYANATES

Номер: US20180009742A1
Принадлежит: BASF SE

The invention relates to polyphenyl polymethylene polyisocyanates having an NCO number of at least 29% comprising less than 2% by weight ureas, less than 8% by weight carbodiimides or uretonimines and less than 1000 ppm organic chlorine compounds. 1. A method for preparing a polyphenyl polymethylene polyisocyanate having an NCO number , determined according to DIN EN ISO 14896 , of at least 29% comprising less than 2% by weight ureas , determined by NMR , less than 8% by weight carbodiimides or uretonimines , determined by NMR , and less than 1000 ppm organic chlorine compounds , determined by high-resolution mass spectrometry or according to ASTM D4663-10 , the method comprising:reacting a polyphenyl polymethylene polyamine with an organic carbonate to give a corresponding polyphenyl polymethylene polycarbamate,thermally cleaving the polyphenyl polymethylene polycarbamate to give the polyphenyl polymethylene polyisocyanate; andprior to the thermally cleaving, reacting free amino groups or urea groups present in a carbamate crude mixture comprising the polyphenyl polymethylene polycarbamate with a derivatizing reagent to give amide groups or urethane groups.2. The method according to claim 1 , wherein the derivatizing reagent comprises at least one selected from the group consisting of an ester claim 1 , an acid anhydride claim 1 , and an acyl chloride of an aliphatic carboxylic acid having 1 to 10 carbon atoms or an aromatic carboxylic acid having 7 to 14 carbon atoms.3. The method according to claim 1 , wherein the derivatizing reagent comprises at least one of acetic anhydride and acetyl chloride.4. The method according to claim 1 , wherein the derivatizing reagent comprises at least one of a chloroformic ester and a pyrocarbonate of C-C-alkanols5. The method according to claim 1 , wherein the reacting of the free amino groups or the urea groups with the derivatizing reagent is carried out in a solvent.6. The method according to claim 5 , wherein the solvent is ...

Подробнее
08-01-2015 дата публикации

Apparatus and method of generating magnetic resonance spectrum

Номер: US20150011863A1
Принадлежит: SAMSUNG ELECTRONICS CO LTD

A method generates a magnetic resonance (MR) spectrum by obtaining an MR echo signal from an object in response to a transmitted radio frequency (RF) signal that is emitted towards the object. The method extracts from the MR signal, a plurality of signals corresponding to a plurality of frequency ranges and adjusts a phase of at least one of the extracted plurality of signals in a time domain. A combination signal is generated by combining the plurality of signals including the at least one extracted phase adjusted signal and generates an MR spectrum of the object in response to the combination signal.

Подробнее
11-01-2018 дата публикации

CHARACTERIZATION OF CRUDE OIL BY NMR SPECTROSCOPY

Номер: US20180011037A1
Принадлежит:

A system and a method for applying C or H NMR spectroscopy to a sample of oil in order to calculate and assign an indicative property such as cetane number, pour point, cloud point, aniline point and/or octane number of a gas oil or naphtha fraction of the crude oil. 1. A system for assigning an indicative property to a fraction of an oil sample based upon nuclear magnetic resonance (NMR) spectroscopy data , the system comprising:a non-volatile memory device that stores calculation modules and data, the data including NMR spectroscopy data indicative of aromatic, naphthenic, paraffinic carbon content of the oil sample;a processor coupled to the memory; anda calculation module that calculates and assigns the indicative property of a fraction of the oil sample as a function of the aromatic, naphthenic, paraffinic carbon content of the oil sample.2. A system for assigning an indicative property to a fraction of an oil sample comprising:a nuclear magnetic resonance (NMR) spectrometer that outputs NMR spectroscopy data;a non-volatile memory device that stores calculation modules and data, the data including outputted NMR spectroscopy data indicative of aromatic, naphthenic, paraffinic carbon content of the oil sample;a processor coupled to the memory; anda calculation module that calculates and assigns the indicative property of a fraction of the oil sample as a function of the aromatic, naphthenic, paraffinic carbon content of the oil sample.3. The system of wherein the calculation module calculates and assigns the indicative property of a fraction of the oil sample as a function of the aromatic claim 1 , naphthenic claim 1 , paraffinic carbon content of the oil sample and the density of the oil sample.4. A method for operating a computer to assign an indicative property to a fraction of an oil sample based upon nuclear magnetic resonance (NMR) spectroscopy data claim 1 , the method comprising:entering into the computer NMR spectroscopy data indicative of the aromatic, ...

Подробнее
12-01-2017 дата публикации

Field-invariant quantitative magnetic-resonance signatures

Номер: US20170011255A1
Принадлежит: Tesla Health Inc

A system that determines an invariant magnetic-resonance (MR) signature of a biological sample is disclosed. During operation, the system determines a magnetic-resonance (MR) model of voxels in a biological sample based on differences between MR signals associated with the voxels in multiple scans and simulated MR signals. The MR signals are measured or captured by an MR scanner in the system during multiple MR scans, and based on scanning instructions, and the simulated MR signals for the biological sample are generated using the MR model and the scanning instructions. Moreover, the system iteratively modifies the scanning instructions (including a magnetic-field strength and/or a pulse sequence) in the MR scans based on the differences until a convergence criterion is achieved. Then, the system stores, in memory, an identifier of the biological sample and a magnetic-field-strength-invariant MR signature of the biological sample that is associated with the MR model.

Подробнее
14-01-2021 дата публикации

IN SITU, REAL-TIME IN-LINE DETECTION OF FILLING ERRORS IN PHARMACEUTICAL PRODUCT MANUFACTURING USING WATER PROTON NMR

Номер: US20210010962A1
Принадлежит:

A method of using the transverse relaxation rate (R) of solvent NMR signal to detect filling errors of an alum-containing product in real-time in-line during manufacturing, for example during a fill-finish unit operation. This technique can be used for quality control in vaccine manufacturing to ensure the delivery of the correct concentration of alum-containing product to the product container such as a vial or pre-filled syringe. 1. A method of detecting a filling error of an alum-containing product in real-time in-line during a fill-finish unit operation , said method comprising:flowing the alum-containing product into a filling conduit, wherein the filling conduit directs the alum-containing product into a vial, and wherein the filling conduit is arranged to flow through a magnet and a probe of nuclear magnetic resonance (NMR) spectrometer prior to the vial;{'sub': '2,m', 'measuring the transverse relaxation rate of solvent Rin the alum-containing product flowing through the filling conduit; and'}{'sub': 2,m', '2,r', '2,r, 'comparing the measured Rto a reference transverse relaxation rate of solvent R, wherein the reference Rrepresents an acceptable flow rate or concentration of aluminum particles in the alum-containing product,'}{'sub': 2,m', '2,r, 'wherein when the measured Ris inside a range of the reference R, there is no filling error.'}2. The method of claim 1 , wherein the Ris measured using nuclear magnetic resonance (NMR).3. The method of claim 1 , wherein the filling conduit delivers product from an upstream large-scale product vessel to a product container.4. The method of claim 1 , wherein the Rcan be measured without withdrawing the alum-containing product from the filling conduit.5. The method of claim 1 , wherein the solvent is water.6. The method of claim 1 , wherein the alum-containing product comprises particles in a range from about 1 nanometer and 50 microns in diameter claim 1 , preferably about 500 nm to about 1000 nm or about 1000 nm to ...

Подробнее
10-01-2019 дата публикации

MAGNETIC RESONANCE CHEMICAL-SHIFT-ENCODED IMAGING METHOD, APPARATUS AND DEVICE

Номер: US20190011515A1

Provided are a magnetic resonance chemical-shift-encoded imaging method, apparatus, and device, belonging to the technical field of magnetic resonance imaging. The method comprises: in a phasor-error plot established on the basis of a two-point magnetic resonance signal model, determining to be an initial seed point a pixel having a unique phasor and causing said plot to reach a minimal local value; according to the initial seed point, estimating the phasor value of a to-be-estimated pixel to obtain a field map; mapping and merging the field map at the highest resolution to obtain a reconstructed field map; determining a reconstructed seed point from the reconstructed field map, and estimating the reconstructed seed point to obtain the phasor value of the reconstructed to-be-estimated pixel; according to the reconstructed seed point and the phasor value of the reconstructed to-be-estimated pixel, obtaining two separate images having predetermined components. In the method, a region simultaneously containing two components is identified as a seed point, eliminating the deviation caused by phasor-value jump at high resolution and ensuring the correctness of the seed point ultimately selected. 1. A magnetic resonance chemical-shift-encoded imaging method , comprising:providing predetermined resolutions;establishing a phasor-error spectrum based on a two-point magnetic resonance signal model in a sampled image at each of the predetermined resolutions;determining to be an initial seed point a pixel point having a unique phasor value in the phasor-error spectrum and enabling the phasor-error spectrum to reach a local minimum value;estimating a phasor value of a to-be-estimated pixel point according to the initial seed point to obtain a field pattern at each of the predetermined resolutions;mapping, at a highest resolution, the field patterns at the predetermined resolutions respectively to obtain a plurality of field patterns at the highest resolution, and merging the ...

Подробнее
11-01-2018 дата публикации

METHOD AND SYSTEM FOR IDENTIFICATION OF METABOLITES

Номер: US20180011990A1
Принадлежит:

A method and system is provided for mass spectrometry for identification of a specific elemental formula for an unknown compound which includes but is not limited to a metabolite. The method includes calculating a natural abundance probability (NAP) of a given isotopologue for isotopes of non-labelling elements of an unknown compound. Molecular fragments for a subset of isotopes identified using the NAP are created and sorted into a requisite cache data structure to be subsequently searched. Peaks from raw spectrum data from mass spectrometry for an unknown compound. Sample-specific peaks of the unknown compound from various spectral artifacts in ultra-high resolution Fourier transform mass spectra are separated. A set of possible isotope-resolved molecular formula (IMF) are created by iteratively searching the molecular fragment caches and combining with additional isotopes and then statistically filtering the results based on NAP and mass-to-charge (m/2) matching probabilities. An unknown compound is identified and its corresponding elemental molecular formula (EMF) from statistically-significant caches of isotopologues with compatible IMFs. 1. A method for mass spectrometry data analysis for identification of a specific elemental molecular formula (EMF) for an unknown compound , the method comprising:calculating a natural abundance probability (NAP) of a given isotopologue for isotopes of non-labeling elements of an unknown compound;creating and sorting caches of molecular fragments for a subset of isotopes identified using the NAP, into a requisite cache data structure, to be searched;characterizing peaks from raw spectrum from mass spectrometry for an unknown compound and separating sample-specific peaks from various spectral artefacts seen in ultra-high resolution Fourier transform mass spectra;creating sets of possible isotope-resolved molecular formulae (IMF) by iteratively searching the molecular fragment caches and combining with additional isotopes and ...

Подробнее
09-01-2020 дата публикации

NMR METHOD FOR DETECTING AND QUANTIFYING INDIVIDUAL ANALYTES IN LIQUID ANALYTE MIXTURES

Номер: US20200011816A1

A method for detection and quantification of individual analytes in liquid analyte mixtures, by means of NMR spectrometry, in which method a sample of the analyte mixture has a high-frequency pulse applied to it in an NMR spectrometer, and the resulting NMR spectrum is evaluated, is to be developed further in such a manner that it allows a precise analysis of liquid analyte mixtures even when using low-field NMR spectrometers. For this purpose, the sample of the analyte mixture is placed into a low-field NMR spectrometer, and at least one high-frequency pulse that excites only one specific analyte is applied to it. 1: A method for detection and quantification of individual analytes in liquid analyte mixtures , by means of NMR spectrometry , in which method a sample of the analyte mixture has a high-frequency pulse applied to it in an NMR spectrometer , and the resulting NMR spectrum is evaluated ,whereinthe sample of the analyte mixture is placed into a low-field NMR spectrometer, and at least one high-frequency pulse that excites only one specific analyte is applied to it.2: The method according to claim 1 , whereinthe sample of the analyte mixture has multiple high-frequency pulses applied to it, one after the other, each pulse exciting only one specific analyte, wherein the resulting NMR spectrum is evaluated after every high-frequency pulse application.3: The method according to claim 1 , whereinthe magnetic field of the low-field NMR spectrometer has a magnetic intensity between 0.1 and 3.0 T.4: The method according to claim 1 , whereina high-frequency pulse that is specific to a respective analyte and excites only this analyte is determined and archived for a plurality of analytes.5: The method according to claim 4 , whereinthe respective high-frequency pulse, which excites only one specific analyte, is determined in numerically iterative manner. The invention relates to a method for detection and quantification of individual analytes in liquid analyte ...

Подробнее
09-01-2020 дата публикации

Method for obtaining a two-dimentional j-resolved nmr spectrum against inhomogeneous magnetic field applied along a single direction

Номер: US20200011817A1
Принадлежит: XIAMEN UNIVERSITY

The present disclosure provides a method for ultrafastly obtaining a two-dimensional J-resolved NMR spectrum with a high-resolution against an inhomogeneous magnetic field. The method utilizes the selective excitation module and the reunion sampling module jointly, which breaks through the limitations of existing methods for obtaining the two-dimensional J-resolved NMR spectrum and effectively eliminates an influence of the inhomogeneous magnetic field along an encoding direction. At the same time, an inhomogeneous magnetic field along x and y directions is theoretically eliminated by a slow rotation of the sample. As a consequence, a two-dimensional J-resolved NMR spectrum with a high resolution is obtained by a single-scanning sampling under the inhomogeneous magnetic field, thus significantly shortening experimental duration and expanding application fields of the two-dimensional J-resolved NMR spectrum. The present disclosure further provides a method using multi-band sampling, which is used to obtain J-resolved NMR spectrum with improved signal-to-noise ratio.

Подробнее
09-01-2020 дата публикации

MEASURING THE WETTABILITY OF POROUS MEDIA BASED ON THE TEMPERATURE SENSITIVITY OF NUCLEAR MAGNETIC RESONANCE RELAXATION TIME

Номер: US20200011818A1
Принадлежит: Saudi Arabian Oil Company

The present disclosure describes methods and systems, including computer-implemented methods, computer program products, and computer systems, for measuring wettability of a rock sample. One method includes: at each temperature of a plurality of temperatures, obtaining a first Nuclear Magnetic Resonance (NMR) surface relaxation time for a rock sample having a saturation level; determining a first temperature sensitivity based on the first NMR surface relaxation times and corresponding temperatures; at each temperature of the plurality of temperatures, obtaining a second NMR surface relaxation time for the rock sample that is saturated with oil; determining a second temperature sensitivity based on the second NMR surface relaxation times and corresponding temperature; and determining a wettability of the rock sample based on the first temperature sensitivity and the second temperature sensitivity. 1. A device for measuring wettability of a rock sample , comprising:at least one hardware processor; anda non-transitory computer-readable storage medium coupled to the at least one hardware processor and storing programming instructions for execution by the at least one hardware processor, wherein the programming instructions, when executed, cause the at least one hardware processor to perform operations comprising:at each temperature of a plurality of temperatures, obtaining a first Nuclear Magnetic Resonance (NMR) surface relaxation time for the rock sample having a saturation level, wherein the first NMR surface relaxation time is determined based on a T1 relaxation time;determining a first temperature sensitivity based on the first NMR surface relaxation times and corresponding temperatures;at each temperature of the plurality of temperatures, obtaining a second Nuclear Magnetic Resonance (NMR) surface relaxation time for the rock sample that is saturated with oil;determining a second temperature sensitivity based on the second NMR surface relaxation times and ...

Подробнее
09-01-2020 дата публикации

MEASURING THE WETTABILITY OF POROUS MEDIA BASED ON THE TEMPERATURE SENSITIVITY OF NUCLEAR MAGNETIC RESONANCE RELAXATION TIME

Номер: US20200011819A1
Принадлежит: Saudi Arabian Oil Company

The present disclosure describes methods and systems, including computer-implemented methods, computer program products, and computer systems, for measuring wettability of a rock sample. One method includes: at each temperature of a plurality of temperatures, obtaining a first Nuclear Magnetic Resonance (NMR) surface relaxation time for a rock sample having a saturation level; determining a first temperature sensitivity based on the first NMR surface relaxation times and corresponding temperatures; at each temperature of the plurality of temperatures, obtaining a second NMR surface relaxation time for the rock sample that is saturated with oil; determining a second temperature sensitivity based on the second NMR surface relaxation times and corresponding temperature; and determining a wettability of the rock sample based on the first temperature sensitivity and the second temperature sensitivity. 1. A non-transitory computer-readable medium storing instructions which , when executed , cause a computing device to perform operations comprising:at each temperature of a plurality of temperatures, obtaining a first Nuclear Magnetic Resonance (NMR) surface relaxation time for a rock sample having a saturation level, wherein the first NMR surface relaxation time is determined based on a T1 relaxation time;determining a first temperature sensitivity based on the first NMR surface relaxation times and corresponding temperatures;at each temperature of the plurality of temperatures, obtaining a second Nuclear Magnetic Resonance (NMR) surface relaxation time for the rock sample that is saturated with oil;determining a second temperature sensitivity based on the second NMR surface relaxation times and corresponding temperature;determining a wettability of the rock sample based on the first temperature sensitivity and the second temperature sensitivity, wherein the wettability is a first wettability;at each temperature of the plurality of temperatures, obtaining a third NMR ...

Подробнее
18-01-2018 дата публикации

POLYETHER-BASED POLYMER COMPOSITION

Номер: US20180016391A1
Принадлежит: ZEON CORPORATION

The present invention is a polyether-based polymer composition includes: a polyether-based polymer including an oxirane monomer unit and having one cationic group substantially only at one terminal of a polymer chain, and a nanocarbon material. The polyether-based polymer composition of the present invention can be suitably used, for example, as a bucky gel or as a master batch for preparing a nanocarbon material aqueous dispersion in which a nanocarbon material is favorably dispersed. 1. A polyether-based polymer composition comprising;a polyether-based polymer including an oxirane monomer unit and having one cationic group substantially only at one terminal of a polymer chain, anda nanocarbon material.4. The polyether-based polymer composition according to claim 3 , wherein R represents a methyl group in the formula (2).5. The polyether-based polymer composition according to claim 1 , wherein the nanocarbon material is a carbon nanotube.6. The polyether-based polymer composition according to claim 1 , wherein a content of the nanocarbon material is 0.01 to 30 parts by weight based on 100 parts by weight of the polyether-based polymer.7. The polyether-based polymer composition according to claim 1 , wherein water is further contained and a content of the nanocarbon material is 0.05wt % or more based on the whole composition. The present invention relates to a polyether-based polymer composition in which a nanocarbon material is favorably and stably dispersed in the polyether-based polymer. The polyether-based polymer composition of the present invention can be suitably used, e.g., as a master batch for preparing a nanocarbon material aqueous dispersion in which the nanocarbon material is favorably dispersed.Since nanocarbon materials such as carbon nanotubes have excellent electrical properties and further have both excellent thermal conductivity and mechanical strength properties, they are expected to be applied in a wide range of fields. As one of methods for ...

Подробнее
17-01-2019 дата публикации

IMIDAZOLINE COMPOUND, MOBILITY CONTROL SYSTEM, PLUGGING AGENT FOR GAS CHANNELING, AND METHOD FOR CARBON DIOXIDE FLOODING

Номер: US20190016683A1
Принадлежит:

An imidazoline compound, a mobility control system, a plugging agent for gas channeling, and a method for carbon dioxide flooding. The structure of the imidazoline compound is represented by formula (1), in which R is pentadecyl, heptadecenyl, or heptadecyl. A mobility control system that contains the imidazoline compound can interact with carbon dioxide to form a plugging agent for gas channeling, and thereby attains a plugging effect for carbon dioxide channeling in a carbon dioxide flooding process. 2. A mobility control system claim 1 , comprising the imidazoline compound of claim 1 , a mobility control additive claim 1 , and water.3. The mobility control system of claim 2 , wherein claim 2 , the mobility control additive is selected from the group consisting of sodium salicylate claim 2 , maleic acid claim 2 , sodium p-toluene sulfonate claim 2 , and combinations thereof.4. The mobility control system of claim 3 , wherein claim 3 , R is pentadecyl claim 3 , and the mobility control additive is sodium p-toluene sulfonate.5. The mobility control system of claim 2 , wherein claim 2 , as percentages of the weight of the mobility control system claim 2 , the content of the imidazoline compound is 1-10 wt. % claim 2 , the content of the mobility control additive is 0.1-2 wt. % claim 2 , and the content of water is 88-98.9 wt. %.6. The mobility control system of claim 5 , wherein claim 5 , as percentages of the weight of the mobility control system claim 5 , the content of the imidazoline compound is 2-6 wt. % claim 5 , the content of the mobility control additive is 0.4-0.8 wt. % claim 5 , and the content of water is 93.2-97.6 wt. %.7. A plugging agent for gas channeling claim 2 , wherein the plugging agent for gas channeling is a mixture obtained by introducing carbon dioxide into the mobility control system of to form a gel.8. The plugging agent for gas channeling of claim 7 , wherein the mobility control additive is selected from the group consisting of sodium ...

Подробнее
28-01-2016 дата публикации

DETECTION OF BRCA CARRIERS IN BREAST TISSUE

Номер: US20160022197A1
Принадлежит:

A method and system for detecting the presence of BRCS carriers in breast tissue, comprises obtaining spectral data from breast tissue using a magnetic resonance spectroscopy device and producing spectral data by said device which provides chemical markers to enable detection of whether the breast tissue contains BRCA carriers. 1. A method of detecting the presence of BRCS carriers in breast tissue , comprising:obtaining spectral data from breast tissue using a magnetic resonance spectroscopy device;producing spectral data by said device which provides chemical markers to enable detection of whether the breast tissue contains BRCA carriers.2. The method of claim 1 , wherein the spectral data is produced using a 2D COSY.3. The method of claim 1 , wherein the step of producing spectral data produces spectral data which enables detection of whether the breast tissue contains BRCA carriers claim 1 , is normal healthy tissue claim 1 , or contains invasive cancer.4. The method of claim 1 , wherein the spectral data produced enables detection of increased saturated lipid and increased membrane cholesterol which is conducive to tumor growth which constitutes a premalignant condition.5. The method of claim 1 , wherein the step of obtaining spectral data from breast tissue comprises obtaining spectral data from a breast tissue in vivo.6. The method of claim 1 , wherein the step of obtaining spectral data from breast tissue comprises obtaining spectral data from a core fine needle biopsy of breast tissue ex vivo.7. The method of claim 1 , wherein the step of producing spectral data includes producing a spectral image on a display.8. A system for detecting the presence of BRCA carriers in breast tissue claim 1 , comprising:a magnetic resonance spectroscopy device for obtaining spectral data from breast tissue, and;a processor for producing spectral data which includes chemical markers to enable detection of whether the breast tissue contains BRCA carriers.9. The system of claim ...

Подробнее
17-04-2014 дата публикации

Method and magnetic resonance apparatus to determine at least one datum from an implanted silicone implant

Номер: US20140107470A1
Принадлежит: Individual

In a method and magnetic resonance apparatus to determine at least one datum of an implanted silicone implant, at least one magnetic resonance data set is acquired, with the acquired signals of the magnetic resonance data set originating at least in part from the silicone implant. At least one spectrum is calculated from the magnetic resonance data set, and the datum is determined in a processor from the spectrum.

Подробнее
17-04-2014 дата публикации

METHOD FOR DETERMINING THE METABOLIC CAPACITY OF AT LEAST ONE ENZYME

Номер: US20140107516A1
Принадлежит: Humedics GmbH

A method for determining the metabolic capacity of an enzyme includes time-resolved determination of the concentration of a product in exhaled air. The product is created by metabolism of a substrate, previously administered to an individual, by an enzyme of the individual. The product concentration is determined until the maximum product concentration in the exhaled air is reached. A model function is fitted to measured values of the product concentration, obtained by the time-resolved determination of the product concentration between start and end times. The metabolic capacity of the enzyme is determined based on parameters of the model function. Determining the metabolic capacity of the enzyme takes place based on at least two parameters of the model function, wherein the maximum value and time constant of the model function are not selected as parameters at the same time, and the start and/or end times are not selected as parameters. 1. A method for determining the metabolic capacity of at least one enzyme , comprising the following steps:time-resolved determination of the concentration of a product in the air exhaled by an individual, wherein the product has been created by a metabolism of a substrate, previously administered to the individual, by at least one enzyme of the individual and wherein the product concentration is determined at the least until the maximum product concentration in the air exhaled by the individual is reached,fitting of a model function to measured values of the product concentration, which were obtained by the time-resolved determination of the product concentration between a start time and an end time, anddetermination of the metabolic capacity of the enzyme on the basis of parameters of the model function, which specify the model function,wherein determining the metabolic capacity of the enzyme takes place on the basis of at least two parameters of the model function, with the proviso that the maximum value of the model function ...

Подробнее
25-01-2018 дата публикации

Bimodal Polypropylene Compositions and Method of Making Same

Номер: US20180022907A1
Принадлежит:

The present invention relates to a bimodal polypropylene composition comprising a blend of a HMW polypropylene component and a LMW polypropylene component, where the high molecular weight (HMW) component of the bimodal composition has a z-average molecular weight Mz of more than 400,000 g/mole, and a process to make such composition. The composition is suitable for thermoformed articles and injection molded articles. 1. A polypropylene composition comprising at least one high molecular weight (HMW) polypropylene component and at least one low molecular weight (LMW) polypropylene component , wherein the polypropylene composition has any one or more of the following features:{'sup': '−1', 'a) an extensional viscosity of the polypropylene composition of more than 10,000 Pa·s, when measured on an extensional rheometer at a temperature of 172° C., and an extensional rate of 10 secondmeasured at 0.3 seconds;'}b) a zero shear viscosity of the polypropylene composition no less than the zero shear viscosity of the HMW polypropylene component alone, as determined in accordance with Small Angle Oscillatory Shear (SAOS) Rheology Test; and/orc) a relaxation time of the polypropylene composition of more than 0.9 seconds, as determined in accordance with Small Angle Oscillatory Shear (SAOS) Rheology Test;wherein the HMW polypropylene component has a z-average molecular weight Mz of more than 400,000 g/mole, as determined by Gel Permeation Chromatography (GPC), and is in an amount in the range of from 80.0 wt % to 99.9 wt %, based on the total weight of the composition.2. The polypropylene composition of claim 1 , wherein the extensional viscosity of the polypropylene composition is more than 20 claim 1 ,000 Pa·s claim 1 , when measured on an extensional rheometer at a temperature of 172° C. claim 1 , and an extensional rate of 10 secondmeasured at 0.3 seconds.3. The polypropylene composition of claim 1 , wherein the zero shear viscosity of the polypropylene composition is at least ...

Подробнее
22-01-2015 дата публикации

Methods for Classifying Pleural Fluid

Номер: US20150025339A1
Автор: Ching-Wan Lam
Принадлежит: University of Hong Kong HKU

Methods of classifying pleural fluid are disclosed. The methods typically include determining the level of indicator nanoparticles, such as lipids, particularly large lipids, in the pleural fluid of a subject. The level of lipids can be determined by nuclear magnetic resonance (NMR), such as proton NMR ( 1 H-NMR) by measuring the NMR signal corresponding to methyl protons, methylene protons, methene protons, or combinations thereof. The level of large lipids in pleural fluid can be carried out in vitro on a sample of pleural fluid obtained from the subject or in vivo using magnetic resonance spectroscopy (MRS). The pleural fluid can be classified as exudate or transudate with a sensitivity, selectivity, or combination thereof of 85%, 90%, 95%, 99%, or higher, a selectivity of 85%, 90%, 95%, 99%. The method can be coupled with diagnosing and/or treating the subject with a disease, disorder, or condition.

Подробнее
26-01-2017 дата публикации

IDENTIFICATION OF BLOOD BASED METABOLITE BIOMARKERS OF PANCREATIC CANCER

Номер: US20170023575A1
Принадлежит: PURDUE RESEARCH FOUNDATION

The present disclosure relates to a panel of a plurality of metabolite species that is useful for the identification or detection of subjects having pancreatic cancer, including methods for identifying such metabolic biomarkers within biological samples. The disclosure also includes a statistical model for predicting the presence of pancreatic cancer in a subject's biofluid by quantifying and comparing positive and negative fold changes in metabolite species' concentration; comparing the subject's metabolite species' concentrations to a predetermined value. 1establishing a training dataset based on measured concentrations of at least two metabolite species based on known pancreatic cancer data, wherein the at least two metabolite species is a component of a panel of a plurality of metabolite species;measuring concentrations of the at least two metabolite species in a sample of a biofluid from a subject;comparing the measured concentration of the at least two metabolite species to the training dataset based on combined regression and univariate analysis, thereby generating a score; andcomparing the score to a score of healthy group in order to predict presence of pancreatic cancer in the subject.. A method for detecting pancreatic cancer in a subject, comprising: The present application is a continuation of U.S. application Ser. No. 14/465,535, filed Aug. 21, 2014, which claims the benefit of U.S. provisional application Ser. No. 61/868,398, filed Aug. 21, 2013, the contents of which are incorporated by reference herein in their entirety.The present disclosure generally relates to small molecule metabolic biomarkers. In particular, the present disclosure relates to a panel of metabolite species that is useful for the identification of subjects having pancreatic cancer, including methods for identifying such metabolic biomarkers within biological samples.Pancreatic cancer (PC) afflicts both men and women, and is the fourth leading cause of cancer related deaths in the ...

Подробнее
28-01-2016 дата публикации

NUCLEAR MAGNETIC RESONANCE APPARATUS AND METHODS

Номер: US20160025825A1
Автор: Taicher Gersh Z.
Принадлежит:

A nuclear magnetic resonance (NMR) apparatus includes at least one magnet configured to induce a static magnetic field in a sample chamber. At least one radio frequency antenna is configured to induce a radio frequency magnetic field in the sample chamber. A surface of a material sample disposed in the sample chamber and an interface with the sample chamber to the material sample volume ratio is selected such that NMR phenomena induced in the material sample depend substantially entirely on the material sample to sample chamber interface effects. 1. A nuclear magnetic resonance (NMR) apparatus , comprising:at least one magnet configured to induce a static magnetic field in a sample chamber;at least one radio frequency antenna configured to induce a radio frequency magnetic field in the sample chamber; andwherein a ratio of a surface of a material sample disposed in the sample chamber and at an interface with the sample chamber with respect to the material sample volume is selected such that NMR phenomena induced in the material sample depend substantially entirely on material sample to sample chamber interface effects.2. The NMR apparatus of wherein the material sample to sample chamber interface effects include changes or rate of changes of at least one of spin-spin relaxation claim 1 , spin-lattice relaxation claim 1 , diffusion constant claim 1 , and maximum NMR signal amplitude.3. The NMR apparatus of wherein the at least one magnet having a longitudinal axis and having a magnetization direction extending substantially perpendicularly to the longitudinal axis and the at least one radio frequency antenna including at least one coil wound in a manner whereby the coil turns lie in planes substantially perpendicular to the longitudinal axis.4. The NMR apparatus of wherein the at least one magnet comprises at least two poles disposed externally to the sample chamber claim 1 , the at least two poles having opposed magnetization directed at each other.5. The NMR ...

Подробнее
28-01-2016 дата публикации

NUCLEAR MAGNETIC RESONANCE APPARATUS AND METHODS

Номер: US20160025826A1
Автор: Taicher Gersh Z.
Принадлежит:

A nuclear magnetic resonance (NMR) apparatus includes at least one magnet arranged to induce a static magnetic field in a sample chamber. The static magnetic field has a known amplitude distribution. At least one radio frequency antenna is configured to induce a radio frequency magnetic field in the sample chamber at a predetermined frequency and a predetermines bandwidth. The static magnetic field amplitude at a sample chamber boundary has substantially at most two values. 1. A nuclear magnetic resonance (NMR) apparatus , comprising:at least one magnet arranged to induce a static magnetic field in a sample chamber, the static magnetic field having a known amplitude distribution;at least one radio frequency antenna configured to induce a radio frequency magnetic field in the sample chamber at a predetermined frequency and a predetermined bandwidth; andwherein a static magnetic field amplitude at a sample chamber boundary has substantially at most two values.2. The method of further comprising forming sample chamber boundaries wherein the static magnetic field amplitude at the boundaries substantially reaching only maximum and minimum of static magnetic field amplitude in the sample chamber.3. The NMR apparatus of wherein a boundary of the least one radio frequency antenna conforms to the sample chamber boundary.4. The NMR apparatus of wherein the at most two values are substantially equal.5. The NMR apparatus of wherein the predetermined frequency corresponding to one of the at most two values of the static magnetic field amplitude and the predetermined bandwidth are selected to excite NMR phenomena substantially exclusively proximate to the sample chamber boundary.6. The NMR apparatus of wherein a material sample is located inside the sample chamber wherein a ratio of a surface of the material sample to sample chamber interface with respect to a volume of the material sample is selected such that NMR phenomena induced in the sample depend substantially entirely on ...

Подробнее
28-01-2016 дата публикации

NUCLEAR MAGNETIC RESONANCE APPARATUS AND METHODS

Номер: US20160025827A1
Автор: Taicher Gersh Z.
Принадлежит:

A nuclear magnetic resonance (NMR) apparatus includes at least one solenoid configured to induce a radio frequency magnetic field in a sample. The sample is located inside the solenoid. At least one cylindrical magnet is arranged to induce a static magnetic field in the sample, wherein the magnet is located inside the sample. 1. A nuclear magnetic resonance (NMR) apparatus , comprising:at least one solenoid configured to induce a radio frequency magnetic field in a sample, wherein the sample is located inside the solenoid; andat least one substantially cylindrical magnet arranged to induce a static magnetic field in the sample, wherein the magnet is located inside the sample.2. The NMR apparatus of wherein a solenoid axis of the at least one solenoid and a cylindrical axis of the at least one substantially cylindrical magnet are parallel to a longitudinal axis of the apparatus.3. The NMR apparatus of wherein the sample is located inside a sample chamber having a longitudinal axis parallel to the longitudinal axis of the apparatus.4. The NMR apparatus of wherein the static magnetic field in the sample is perpendicular to the longitudinal axis of the apparatus.5. The NMR apparatus of wherein the radio frequency magnetic field in the sample is parallel to the longitudinal axis of the apparatus.6. The NMR apparatus of wherein the cylindrical magnet further comprises a magnet uniformly polarized transversely to the longitudinal axis of the apparatus.7. The NMR apparatus of wherein the static magnetic field in the sample has a static magnetic field gradient perpendicular to the longitudinal axis of the apparatus.8. The NMR apparatus of wherein the cylindrical magnet comprises a magnet polarized along the longitudinal axis of the apparatus.9. The NMR apparatus of wherein the static magnetic field in the sample is perpendicular to the longitudinal axis of the apparatus claim 8 , has a radial direction and substantially equal amplitude.10. The NMR apparatus of wherein the ...

Подробнее
25-01-2018 дата публикации

Lipid, protein, and metabolite markers for the diagnosis and treatment of prostate cancer

Номер: US20180024132A1

Methods for diagnosing the presence of prostate cancer in a subject are provided, such methods including the detection of levels of a variety of biomarkers diagnostic of prostate cancer. The invention also provides methods of treating prostate cancer by administering a biomarker or an agent that modulates a biomarker of prostate cancer. Compositions in the form of kits and panels of reagents for detecting the biomarkers of the invention are also provided.

Подробнее
10-02-2022 дата публикации

Multi-Parameter Metabolic Vulnerability Index Evaluations

Номер: US20220043013A1
Принадлежит: Liposcience Inc

Disclosed are methods and systems to determine a subject's metabolic vulnerability index (MVX) score using at least one defined mathematical model of risk. The methods comprise evaluating various biomarkers to distinguish various health risks. In one embodiment, the method comprises evaluating biomarkers to determine a relative risk of premature all-cause mortality. The model may include NMR-derived measurements of GlycA, S-HDLP, branched chain amino acids (BCAAs), ketone bodies, total serum protein, and citrate in at least one biosample of the subject.

Подробнее
10-02-2022 дата публикации

NMR Analyzers for Clinical Evaluation of Biosamples

Номер: US20220043086A1
Принадлежит: LipoScience, Inc.

The clinical analyzers automatically electronically monitor selected parameters and automatically electronically adjust parameters to maintain the analyzer within desired operational ranges. The clinical NMR analyzers can be configured as a networked system with a plurality of clinical NMR analyzers located at different use sites. 1. A networked system of clinical NMR analyzers , comprising:a plurality of clinical NMR analyzers located at different local use sites; andat least one remote control system in communication with the plurality of clinical NMR analyzers configured to monitor selected local operating parameters associated with each clinical NMR analyzer.2. A system according to claim 1 , wherein each of the clinical NMR analyzers includes a high field NMR superconducting magnet claim 1 , and wherein the remote system automatically obtains data corresponding to homogeneity of the magnetic field generated by the superconducting magnet.3. A system according to claim 1 , wherein the clinical NMR analyzers generate and store an electronic history file of selected operational parameters claim 1 , the history file configured to be accessed by the remote system.4. A system according to claim 1 , wherein the clinical NMR analyzers and/or remote system are configured to automatically monitor process variables and statistically analyze data corresponding to measurements of the monitored process variables to thereby perform an automated quality control analysis.5. A system according to claim 4 , wherein the clinical NMR analyzers are configured to automatically adjust operating equipment to keep the process variables within a predetermined statistical variation responsive to the monitored data.6. A system according to claim 1 , wherein the clinical NMR analyzers are configured to automatically generate an alert when an abnormal operating condition is detected.7. A system according to claim 1 , wherein the remote system is configured to automatically generate an alert ...

Подробнее
01-02-2018 дата публикации

SYSTEM AND NON-INVASIVE METHOD FOR EXAMINING AT LEAST PARTS OF BLOOD FRACTIONS, AND USE OF THE SYSTEM

Номер: US20180028100A1
Принадлежит:

The invention relates to a system and a non-invasive method for examining at least parts of the blood fractions, designed for examination of the blood fractions on the basis of at least one magnetic resonance spectroscopy of a human body part, in particular of the human finger. The invention also relates to the use of said system. 1. An arrangement for noninvasively examining at least parts of blood constituents ,wherein the arrangement is configured to examine the blood constituents based on at least magnetic resonance spectroscopy of a part of a human body.2. The arrangement of claim 1 , wherein the arrangement is configured for the examination by capture of at least one blood substance based on at least magnetic resonance spectroscopy.3. The arrangement of claim 1 , wherein the arrangement is configured for the examination by capture of at least the blood sugar concentration based on at least magnetic resonance spectroscopy.4. The arrangement of claim 1 , wherein the arrangement is configured for the examination by capture of at least one blood substance claim 1 , at least via a marker substance that correlates with the blood substance claim 1 , based on at least magnetic resonance spectroscopy.5. The arrangement of claim 1 , wherein the arrangement is configured for the examination by capture of the blood substance glucose via at least one marker substance that correlates with the blood substance glucose claim 1 , based on at least magnetic resonance spectroscopy.6. The arrangement of claim 1 , wherein the arrangement is configured for the examination by capture of the blood sugar metabolism claim 1 , via at least a correlating marker substance claim 1 , based on at least magnetic resonance spectroscopy claim 1 , andwherein the arrangement is configured with means for evaluating the capture, the means for evaluating being configured such that the blood sugar concentration is derived from the spectrum that belongs to the marker substance.7. The arrangement of ...

Подробнее
02-02-2017 дата публикации

Device for Subdividing Magnetic Field and Simultaneous Detection of Magnetic Resonance Signals from Multiple Sample Compartments

Номер: US20170030985A1
Автор: Gerald, II Rex E.

Devices and methods are provided for simultaneously interrogating multiple samples using NMR spectroscopy. A first magnetic field is induced. A flow of electricity is induced through a conductive material. The flow of electricity has a direction that is perpendicular to the first magnetic field, and the flow of electricity induces a second magnetic field. A first sample is placed in an additive magnetic field region, where a direction of the first magnetic field and a direction of the second magnetic field are aligned within the additive magnetic field region. A second sample is placed in a canceling magnetic field region, where the direction of the first magnetic field and the direction of the second magnetic field are opposed within the canceling magnetic field region. A free induction decay (FID) of at least the first and second samples is induced. 1. A method of simultaneously interrogating multiple samples using NMR spectroscopy , the method comprising:inducing a first magnetic field;inducing a flow of electricity through a conductive material, wherein the flow of electricity induces a second magnetic field;placing a first sample in an additive magnetic field region, wherein a direction of the first magnetic field and a direction of the second magnetic field are aligned within the additive magnetic field region;placing a second sample in a canceling magnetic field region, wherein the direction of the first magnetic field and the direction of the second magnetic field are opposed within the canceling magnetic field region; andinducing a free induction decay (FID) of at least the first and second samples.2. The method of claim 1 , further comprising generating a graph of an NMR spectrum for at least the first and the second samples.3. The method of claim 2 , wherein the graph of the NMR spectrum has a signal intensity axis and a chemical shift axis claim 2 , and wherein the NMR spectrum comprises at least a first spectrum and a second spectrum claim 2 , the first ...

Подробнее
04-02-2016 дата публикации

METHOD FOR THE GENERATION OF RADICALS FOR DYNAMIC NUCLEAR POLARIZATION AND USES THEREOF FOR NMR, MRS AND MRI

Номер: US20160033590A1

A method for the preparation of a sample comprising highly polarized nuclear spins is proposed, comprising at least the following steps: 1. A method for the preparation of a sample comprising highly polarized nuclear spins , comprising at least the following steps:a) provision of molecules in the solid state selected from the group consisting of: molecules with 1,2-dione structural units, molecules with 2,5-diene-1,4-dione structural units, and combinations thereof;b) generation of radicals from these molecules in the solid state by photo induced electron transfer by a first electromagnetic irradiation in the visible or ultraviolet frequency range;c) dynamic nuclear polarization in the presence of a magnetic field in the solid state by applying a second electromagnetic irradiation with a frequency adapted to transfer spin polarization from the electrons to the nuclear spins leading to a highly polarized state thereof.2. The method according to claim 1 , wherein the first electromagnetic irradiation is applied with a frequency essentially equal to the difference or the sum of the Larmor frequencies of the electron spins and the nuclear spins claim 1 , respectively claim 1 , in the presence of the applied magnetic field.3. The method according to claim 1 , wherein the first and second electromagnetic irradiation in steps b) and c) are applied sequentially.4. The method according to claim 3 , wherein for the first irradiation one claim 3 , two or more light sources are used in pulsed mode operation forming trains of light pulses of different photon energies claim 3 , different pulse intensities claim 3 , different pulse lengths or combinations thereof claim 3 , that either overlap or are separated in time in order to optically pump the electronic transitions to reach the reactive molecular state.6. The method according to claim 5 , wherein the molecules are isotopically enriched.7. The method according to claim 1 , wherein the molecules are selected from the group ...

Подробнее
04-02-2016 дата публикации

Devices for Use in Solid-State NMR Analysis

Номер: US20160033599A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

The present disclosure relates to devices and methods for use in SSNMR analysis of solid particulate samples. These devices and methods are configured to contain a solid particulate sample as it undergoes SSNMR analysis while also operating to attenuate peak broadening in the resulting spectrum due to anisotropic dipole coupling interactions and CSA during such analysis by generating a substantially fluidized bed of the solid particulate sample. 1. A device for attenuating peak broadening during NMR analysis of a solid particulate sample comprising:(A) a sample container having an inner wall and sized to hold the solid particulate sample;(B) a motor;(C) a non-magnetic, electrically non-conductive drive shaft having a first end and a second end, wherein the motor is fixably attached to the first end of the non-magnetic, electrically non-conductive drive shaft; and(D) a non-magnetic, electrically non-conductive impeller, wherein the non-magnetic, electrically non-conductive impeller is fixably attached to the second end of the non-magnetic, electrically non-conductive drive shaft and the non-magnetic impeller is located inside the sample container.2. The device of claim 1 , wherein the motor is non-magnetic and electrically non-conductive.3. The device of claim 1 , wherein the motor is gas-driven.4. The device of claim 1 , wherein the motor is magnetic and/or electrically-driven and is located at a distance from the sample container corresponding to a magnetic field strength of a corresponding NMR magnetic field of about 0.5 millitesla or less.5. The device of claim 1 , wherein the motor is magnetic and/or electrically-driven and is shielded from the NMR magnet.6. The device of claim 5 , wherein the shielding is active.7. The device of claim 5 , wherein the shielding is passive.8. The device of claim 1 , wherein the non-magnetic claim 1 , electrically non-conductive shaft is flexible.9. The device of claim 1 , wherein the non-magnetic claim 1 , electrically non- ...

Подробнее
01-02-2018 дата публикации

Magnetic coupling high resolution nuclear magnetic resolution probe and method of use

Номер: US20180031499A1
Автор: Albert Zens
Принадлежит: Jeol Ltd

In an embodiment of the invention inductive coupling of an idler coil to a parent coil is used to provide a double resonance circuit without the disadvantages of capacitive coupling to the parent coil. In an embodiment of the invention, an inductive coupling coil can be used to achieve a double-tuned circuit. In an embodiment of the invention, a circuit uses inductive coupling to achieve a double resonance circuit for 1 H, 19 F, and 13 C experiments where one of the three nuclei are observed and the other two are decoupled. In an embodiment of the invention a pivot or a shunt can be used to couple and decouple the idler coil and the parent coil.

Подробнее
01-02-2018 дата публикации

MR FINGERPRINTING FOR DETERMINING PERFORMANCE DEGRADATION OF THE MR SYSTEM

Номер: US20180031653A1
Принадлежит:

The invention provides for a method of operating a magnetic resonance system for acquiring magnetic resonance data () from a phantom () within a measurement (zone ). The phantom comprises a known volume of at least one predetermined substance ((), ). The method comprises the step of acquiring () the magnetic resonance data by controlling the magnetic resonance system with pulse sequence instructions (). The pulse sequence instructions cause the magnetic resonance system to acquire the magnetic resonance data according to a magnetic resonance fingerprinting technique. The pulse sequence instructions specify a train of pulse sequence repetitions. Each pulse sequence repetition has a repetition time chosen from a distribution of repetition times. Each pulse sequence repetition comprises a radio frequency pulse chosen from a distribution of radio frequency pulses. The distribution of radio frequency pulses cause magnetic spins to rotate to a distribution of flip angles. Each pulse sequence repetition comprises a sampling event where the magnetic resonance signal is sampled for a predetermined duration at a sampling time before the end of the pulse sequence repetition. The method further comprises determining () one or more performance degradation conditions of the magnetic resonance system by comparing the magnetic resonance data with a magnetic resonance fingerprinting dictionary (). The magnetic resonance fingerprinting dictionary contains a listing of magnetic resonance signals for a set of system states in response to execution of the pulse sequence instructions for each of the at least one predetermined substance. 1. A method of operating a magnetic resonance system for acquiring magnetic resonance data from a phantom within a measurement zone , wherein the phantom comprises a known volume of at least one predetermined substance , wherein the method comprises the steps of:acquiring the magnetic resonance data by controlling the magnetic resonance system with pulse ...

Подробнее
01-02-2018 дата публикации

SYSTEM AND METHOD FOR MAGNETIC RESONANCE IMAGE ACQUISITION

Номер: US20180031654A1
Принадлежит:

A system and method of acquiring an image at a magnetic resonance imaging (MRI) system is provided. Accordingly, an analog signal based on a pulse sequence and a first gain is obtained. The analog signal is converted into a digitized signal. A potential quantization error is detected in the digitized signal based on a boundary. When the detection is affirmative, a replacement analog signal based on the pulse sequence is received. At least one portion of the replacement analog signal can be based on an adjusted gain. The adjusted gain is a factor of the first gain. The replacement analog signal is digitized into a replacement digitized signal. At least one portion of the replacement digitized signal corresponding to the at least one portion of the replacement analog signal is adjusted based on a reversal of the factor. 112-. (canceled)13. A magnetic resonance imaging (MRI) system comprising a data processing system , an analog to digital converter (ADC) , a main field magnet , gradient coils and radio frequency coils , the MRI system configured to perform a method comprising:receiving an analog signal based on a pulse sequence and a first gain;digitizing, by said ADC, the analog signal into a digitized signal;detecting a potential quantization error in the digitized signal based on a boundary;when the detecting is affirmative:receiving a replacement analog signal based on the pulse sequence, at least one portion of the replacement analog signal being based on an adjusted variable gain, the adjusted gain being a factor of the first gain;digitizing, by the ADC, the replacement analog signal into a replacement digitized signal; andadjusting at least one portion of the replacement digitized signal corresponding to the at least one portion of the replacement analog signal, based on a reversal of the factor.14. A non-transient computer program product comprising computer executable instructions , the instructions , when executed by a computer , performing a method ...

Подробнее
31-01-2019 дата публикации

ESTIMATING FORMATION PROPERTIES USING SATURATION PROFILES

Номер: US20190033238A1
Принадлежит:

Methods estimating a property of a porous media include: saturating a sample of the porous media; spinning the sample in a centrifuge with a first end of the sample closer to an axis of rotation of the centrifuge than a second end of the sample; obtaining a first estimate of the first property; saturating the sample of the porous media; spinning the sample in a centrifuge with the second end of the sample closer to the axis of rotation of the centrifuge than the first end of the sample; obtaining a second estimate of the first property; and determining the second property of the porous media based at least in part on the first estimate of the first property and the second estimate of the first property. The first property can be a Tdistribution and the second property can be a Tcutoff 1. A method of estimating a Tcutoff of a porous media , the method comprising:saturating a sample of the porous media with a fluid;{'sub': '2', 'measuring a Tdistribution of the sample while saturated;'} spinning the sample in a centrifuge with a first end of the sample closer to an axis of rotation of the centrifuge than a second end of the sample;', 'obtaining a saturation profile of the sample; and', 'identifying a first low-saturation portion of the sample;, 'preparing the sample for unsaturated measurement by{'sub': '2', 'measuring a Tdistribution of the porous media on the first low-saturation portion of the sample;'}{'sub': 2', '2', '2, 'obtaining a first estimate of the Tcutoff of the porous media by comparing the Tdistribution measured on the first low-saturation portion of the sample with the Tdistribution measured under saturated conditions;'}saturating the sample of the porous media with the fluid;{'sub': '2', 'measuring a Tdistribution of the sample while saturated;'} spinning the sample in a centrifuge with the second end of the sample closer to the axis of rotation of the centrifuge than the first end of the sample;', 'obtaining a saturation profile of the sample; and', ...

Подробнее
31-01-2019 дата публикации

RAPID QUANTIFICATION OF COMPONENTS IN SOLID MIXTURES OF CHEMICALS VIA TIME-DOMAIN NMR SPECTROSCOPY

Номер: US20190033240A1
Автор: JEHLE Stefan, STUEBER Dirk
Принадлежит:

There is described a method for determining the relative quantities of the expected components in a multi-component mixture of solids. The proposed quantification method makes use of a time domain nuclear magnetic resonance (TD-NMR) spectrometer and requires that, for each of the expected components in the mixture, a T1 saturation recovery curve (SRCi) is measured and recorded. The saturation recovery curve for the mixture sample (SRCmix) is determined from a measurement of the sample with the spectrometer. The relative amounts of the expected components present in the mixture sample are determined by fitting a linear combination of the component SRCs (SRCi) to the SRCmix. The resulting value of each weighting coefficient in the fit provides the relative proportion of the corresponding component in the overall sample. 1. A method of determining the relative quantities of a plurality of expected components in a sample using a time-domain nuclear magnetic resonance (TD-NMR) spectrometer , the method comprising:a) obtaining a component saturation recovery curve (SRC) for each of the components;{'sub': 'mix', 'b) measuring the sample using a TD-NMR spectrometer and obtaining a mixture saturation recovery curve (SRC) therefrom; and'}{'sub': 'mix', 'c) fitting to the SRCa linear combination of the component SRCs, each scaled by a weighting coefficient, the respective weighting coefficients being indicative of the relative quantities of the plurality of expected components in the sample.'}2. The method of wherein obtaining a component saturation recovery curve (SRC) for each of the components comprises measuring the component using the TD-NMR spectrometer.3. The method of claim 1 , wherein fitting to the SRCa linear combination of the component SRCs comprises identifying the weighting coefficients that minimize a representative value of a difference vector between the SRCand the linear combination of the component SRCs.4. The method of claim 3 , wherein minimizing the ...

Подробнее
31-01-2019 дата публикации

STEADY STATE MAGNETIC RESONANCE FINGERPRINTING

Номер: US20190033413A1
Принадлежит: KONINKLIJKE PHILIPS N.V.

The invention provides for a magnetic resonance imaging system () for acquiring magnetic resonance data () from a subject () within a measurement zone (), wherein the magnetic resonance imaging system comprises: a processor () for controlling the magnetic resonance imaging system and a memory () for storing machine executable instructions () and pulse sequence commands (). The pulse sequence commands for controlling the magnetic resonance imaging system to acquire the magnetic resonance data according to a magnetic resonance fingerprinting protocol. The pulse sequence commands are configured for controlling the magnetic resonance imaging system to generate an RF pulse train (). The pulse sequence commands are configured for controlling the magnetic resonance imaging system to acquire the magnetic resonance data as multiple k-space traces. The pulse sequence commands are configured for controlling the RF pulse train to be repeated for the acquisition of each of the multiple k-space traces. The machine executable instructions causes the processor to: sequentially acquire () the multiple k-space traces of magnetic resonance data by controlling the magnetic resonance imaging system with pulse sequence commands and calculate () the abundance of each of a set of predetermined substances for k-space traces that are acquired after a predetermined number of k-space traces of the multiple k-space traces has been acquired. The abundance of each of a set of predetermined substances is determined by comparing the magnetic resonance data with a steady state magnetic resonance fingerprinting dictionary (). The steady state magnetic resonance fingerprinting dictionary contains a listing of calculated magnetic resonance signals in response to the RF pulse train for a set of predetermined substances. 1. A magnetic resonance imaging system for acquiring magnetic resonance data from a subject within a measurement zone , wherein the magnetic resonance imaging system comprises:a ...

Подробнее
30-01-2020 дата публикации

CELL FOR NUCLEAR MAGNETIC RESONANCE MEASUREMENT IN A LIQUID MEDIUM, SYSTEM COMPRISING SUCH A CELL AND THE USE THEREOF

Номер: US20200033427A1
Принадлежит:

A liquid-state nuclear-magnetic-resonance measurement cell includes a reservoir for a liquid medium; a fluidic circuit connected to the reservoir and comprising a measurement chamber; a gas injector opening into the fluidic circuit, at a distance from the measurement chamber; and a coil encircling the measurement chamber; wherein it also comprises at least one capacitive element forming, with the coil, an electromagnetic resonator; and in that it has a shape allowing its introduction into a nuclear-magnetic-resonance probe in replacement of an assembly formed by a nuclear-magnetic-resonance tube and a spinner bearing the tube, the coil encircling the measurement chamber being then positioned so as to couple by induction to at least one radiofrequency coil of the probe. Nuclear-magnetic-resonance measurement system comprising such a measurement cell. Magnetic-resonance measurement method using such a cell is also provided. 1. A liquid-state nuclear-magnetic-resonance measurement cell comprising:a reservoir for a liquid medium;a fluidic circuit connected to said reservoir and comprising a measurement chamber;a gas injector opening into said fluidic circuit, at a distance from said measurement chamber; anda coil encircling said measurement chamber; whereinit also comprises at least one capacitive element forming, with said coil, an electromagnetic resonator;in that:it has a shape allowing its introduction into a nuclear-magnetic-resonance probe in replacement of an assembly formed by a nuclear-magnetic-resonance tube and a spinner bearing said tube, the coil encircling the measurement chamber then being positioned so as to couple by induction to at least one radiofrequency coil of said probe;and in thatthe coil is placed in a portion of the cell intended to occupy, in the interior of the probe, a location provided for the nuclear-magnetic-resonance tube, whereas the reservoir and the gas injector are placed in another portion (R) of the cell intended to occupy, in the ...

Подробнее
30-01-2020 дата публикации

Methods for Pre-processing Magnetic Resonance 2-D Correlation Spectroscopy (COSY) Signals to Enhance Data Quality

Номер: US20200033430A1
Принадлежит:

A 2-D MRS (magnetic resonance spectroscopy), or equivalently, NMR (nuclear magnetic resonance), pre-processing method produces clean MRS signals from raw data for possible use, among other applications, for diagnoses of neurological disorders such as PTSD and mTBI of the brain. The specific 2-D MRS data referred to in this invention are the 2-D MRS Correlation Spectroscopy or 2-D COSY data. 1. A magnetic resonance spectroscopy (MRS) pre-processing system , comprising:one or more MRS machines that produce raw two dimensional (2-D) correlation spectroscopy (COSY) MRS data obtained from a pool of subjects; anda computer system executing a pre-processing tool that pre-processes the raw 2-D COSY MRS data to produce clean 2-D COSY signals by performing channel weighting, spectral registration, apodization, zero-filling in the time domain, conversion to the frequency domain, and adjustment of the peak locations using known metabolites.2. A system as claimed in claim 1 , wherein the channel weighting of raw data is singular value decomposition (SVD)-based channel weighting.3. A system as claimed in claim 1 , wherein the spectral registration is performed on multiple iterations of raw data of a subject to correct for drift across the iterations.4. A system as claimed in claim 3 , further comprising averaging the registered iterations.5. A system as claimed in claim 1 , wherein the spectral registration is performed in the time domain.6. A system as claimed in claim 1 , wherein apodization includes applying a Tukey window filter.7. A system as claimed in claim 1 , wherein the known metabolites include N-acetylaspartate (NAA) claim 1 , creatine (Cre) claim 1 , and choline (Cho).8. A system as claimed in claim 1 , wherein adjustment of the peak locations using known metabolites comprises mapping non-uniformly spaced piecewise ppm axes claim 1 , and corresponding spectral values in the F1-F2 plane to uniformly spaced ppm axes using interpolation.9. A system as claimed in claim 1 ...

Подробнее
01-05-2014 дата публикации

Nmr systems and methods for the rapid detection of analytes

Номер: US20140120523A1
Принадлежит: T2 Biosystems Inc

This invention features systems and methods for the detection of analytes, and their use in the treatment and diagnosis of disease.

Подробнее
08-02-2018 дата публикации

Esterified acids for use in polymeric materials

Номер: US20180037695A1
Принадлежит: Zephyros Inc

The present teachings contemplate a method that includes a step of providing a first amount of esterified reaction product of an acid and an epoxy-based material. The esterified reaction product may be further reacted an epoxy resin to form a polymeric epoxy. The resulting material may have a generally linear backbone, foaming and curing capability and flame retardant properties,

Подробнее
11-02-2016 дата публикации

Creation of Nearly-Equivalent Nuclear Spin Singlet States Using Spin-Lock Induced Crossing

Номер: US20160041241A1

Methods and systems for Nuclear Magnetic Resonance (NMR) spectra of samples having unresolved peaks are described. The methods and systems allow for the creation nuclear spin singlet states in nearly-equivalent spin pairs, for example, using continuous spin-locking with a nutation frequency matched to the coupling strength between spins. The invention relates generally to the field Nuclear Magnetic Resonance (NMR). Nuclear magnetic resonance (NMR) spectroscopy can be used as a tool for determining the chemical structure and/or geometry of a molecule in a sample. In many samples, however, resonance frequencies of different nuclei fully or partially overlap, which makes chemical identification of molecule(s) in a sample difficult or impossible. 1. A method comprising selectively creating a nuclear spin singlet state in a target molecule by applying spin-locking with a nutation frequency matched to the J-coupling between two nuclei of interest for a duration appropriate for the resonance frequency difference between the nuclei of interest.2. The method of claim 1 , wherein magnetization is transferred from a triplet state to the singlet state during spin-locking.3. The method of claim 1 , further comprising allowing the nuclear spin singlet state to evolve for a predetermined period of time.4. The method of claim 3 , further comprising transferring the nuclear spin singlet state back to transverse magnetization by applying the spin-locking with the nutation frequency matched to the J-coupling between two nuclei of interest for a duration appropriate for the resonance frequency difference between the nuclei of interest.5. The method of claim 1 , further comprising detecting the nuclear spin singlet state.6. The method of claim 1 , wherein spin-locking comprises applying a weak radio frequency (RF) field.7. The method of claim 1 , wherein the method is carried out by selectively applying a pulse sequence to the target molecule claim 1 , the pulse sequence having ...

Подробнее
11-02-2016 дата публикации

Two-Dimensional Semi-LASER Correlation Spectroscopy with Well-Maintained Cross Peaks

Номер: US20160041243A1
Автор: Yang Shaolin

A sLASER-first-COSY sequence is disclosed. After a delay time, Δ, from application of a first 90° radio frequency (RF) pulse, a first pair of adiabatic full-passage (AFP) pulses are applied to an object in a MRI scanner. The first 90° RF pulse is a non-adiabatic slice-selective 90° RF pulse and the first pair of AFP pulses is separated by an inter-pulse time interval, Δ. A second pair of AFP pulses, separated by the time Δ, is then applied, followed by a second 90° RF pulse. The second 90° RF pulse is a non-adiabatic non-slice-selective 90° RF pulse. MR signal is acquired after an echo time (TE) from application of the excitation RF pulse. The present method may achieve intended full magnetization transfer between a coupled spin pair of a metabolite and maintain metabolite cross peak intensity of a coupled spin pair of a metabolite in the object. 1. In a magnetic resonance imaging (MRI) scanner system , a computer-implemented method comprising:applying to an object in the MRI scanner system a first 90° radio frequency (RF) pulse, wherein the first 90° RF pulse is a non-adiabatic slice-selective 90° RF pulse;{'sub': 1', '2, 'after a delay time, Δ, from application of the first 90° RF pulse, applying to the object, a first pair of adiabatic full-passage (AFP) pulses, wherein the first pair of AFP pulses is separated by an inter-pulse time interval, Δ;'}{'sub': '2', 'applying to the object, a second pair of AFP pulses, wherein the second pair of AFP pulses is separated by the time Δ;'}applying to the object a second 90° RF pulse, wherein the second 90° RF pulse is a non-adiabatic non-slice-selective 90° RF pulse; andacquiring magnetic resonance (MR) signal after an echo time (TE) from application of the excitation RF pulse.2. The method of claim 1 , wherein the second pair of AFP pulses is applied to the object after a time 2Δfrom application of the first pair of AFP pulses.3. The method of claim 1 , wherein the second 90° RF pulse is applied to the object after a time ...

Подробнее
12-02-2015 дата публикации

Method for Substance Identification From NMR Spectrum

Номер: US20150042328A1
Принадлежит: Numares AG

The present invention relates to a method which allows for an automatic substance identification on the basis of an NMR spectrum. In the scope of the method, determining a multitude of integral ratio values, in each case from at least two integral values of the NMR spectrum, takes place, wherein each integral ratio value specifies the ratio of the height and/or area of the underlying spectral values, and determining a multitude of distance values, in each case from at least two position values of the NMR spectrum, takes place, wherein each distance value specifies the spectral distance between the underlying spectral values. The integral ratio values and the distance values are then used for substance identification. 1. A method for the identification of a substance in a sample , comprising the following steps:a) providing an NMR spectrum of a sample containing at least one substance having at least one NMR-active nucleus,b) converting the NMR spectrum into discrete spectral values, wherein each spectral value has an integral value, specifying the height and/or the area of an individual line of the NMR spectrum or of an individual spectral section of the NMR spectrum, and a position value, specifying the mean position of the line considered or of the considered spectral section in the NMR spectrum,c) determining a multitude of integral ratio values, in each case from two integral values of the NMR spectrum, wherein each integral ratio value specifies the ratio of the height and/or of the area of the underlying spectral values,d) determining a multitude of distance values, in each case from two position values of the NMR spectrum, wherein each distance value specifies the spectral distance between the underlying spectral values,d) comparing the integral ratio values of the NMR spectrum with corresponding integral ratio values of an NMR reference spectrum of at least one reference substance,f) selecting a first proper subset from the integral ratio values of the NMR ...

Подробнее
12-02-2015 дата публикации

Nuclear Singlet States as a Contrast Mechanism for NMR Spectroscopy

Номер: US20150042331A1

Methods and systems for Nuclear Magnetic Resonance (NMR) spectra of complex chemical mixtures are described. The methods and systems allow undesired NMR spectral background to be removed or suppressed and target spectral peaks to be uncovered, for example, when strong background signals overlap weaker peaks. In some embodiments, the methods and systems employ a quantum filter utilizing nuclear spin singlet states. 1. A method comprising:selectively creating a nuclear spin singlet state in a target molecule, so as to detect presence of the target molecule within a sample, wherein the sample contains a mixture of molecules and includes at least some background molecules that are different from the target molecule; andpreserving spin polarization of the singlet state while saturating the spin magnetizations of background molecules, so as to suppress spectroscopic signals from the background molecules and to enhance spectroscopic contrast between the target molecule and the background molecules.2. The method of claim 1 , wherein the act of selectively creating the nuclear spin singlet state comprises:applying to the target molecule a sequence of pulses having parameters that are optimized so as to achieve the desired nuclear spin singlet state in the target molecule while minimizing singlet nature of the nuclear spin states of the background molecules.3. The method of claim 1 , further comprising converting the spin polarization of the singlet state back to transverse magnetization for signal readout claim 1 , by controllably applying RF (radiofrequency) pulses.4. The method of claim 1 , wherein the act of preserving spin polarization of the singlet state while saturating spin magnetization of the background molecules comprises:applying a substantially continuous spin-locking RF field.5. The method of claim 1 , wherein the act of saturating spin magnetization of background molecules comprises:using a polyhedral, spherically symmetric phase cycle that substantially ...

Подробнее
18-02-2021 дата публикации

NMR DEVICE FOR DETECTION OF ANALYTES

Номер: US20210048491A1
Автор: Lee W. David
Принадлежит:

This invention relates generally to detection devices having one or more small wells each surrounded by, or in close proximity to, an NMR micro coil, each well containing a liquid sample with magnetic nanoparticles that self-assemble or disperse in the presence of a target analyte, thereby altering the measured NMR properties of the liquid sample. The device may be used, for example, as a portable unit for point of care diagnosis and/or field use, or the device may be implanted for continuous or intermittent monitoring of one or more biological species of interest in a patient. 129-. (canceled)30. A tube for holding a liquid sample , the tube having a varying cross section , wherein the tube is contained within a device configured for detection of an analyte using NMR , said device comprising a plurality of wells for holding a liquid sample comprising magnetic particles and said analyte , said magnetic particles having binding moieties linked thereto , and , for each of said wells: an RF coil disposed about said well , said RF coil configured to detect an echo response produced by exposing said liquid sample in said well to a bias magnetic field created using one or more magnets and an RF excitation.31. A membrane analyte concentrator for concentrating an analyte , wherein the membrane analyte concentrator comprises a chamber , wherein the chamber comprises nanoparticles and a molecular filter configured to keep molecules of interest in the chamber.32. A device for the detection of one or more analytes in a sample from a subject suspected of having sepsis or septic shock , the device comprising:(a) a permanent magnet defining a magnetic field;(b) a support defining a well for holding a liquid sample comprising magnetic particles and the one or more analytes and having an RF coil disposed about the well, the RF coil configured to detect an echo response produced by exposing the liquid sample to a bias magnetic field created using the permanent magnet and an RF ...

Подробнее
15-02-2018 дата публикации

STRUCTURE AND FUNCTION OF THE SALICYCLIC ACID BINDING SITES ON HUMAN HMGB1 AND METHODS OF USE THEREOF FOR THE RATIONAL DESIGN OF BOTH SALICYCLIC ACID DERIVATIVES AND OTHER AGENTS THAT ALTER ANIMAL AND PLANT HMGBS ACTIVITIES

Номер: US20180045715A1
Принадлежит:

Compositions and methods for identifying agents which 1) mimic salicyclic acid binding to human, animal and plant high mobility group box proteins or 2) alter activities of these HMGBs by binding in or around their salicyclic acid-binding sites and agents so identified are disclosed. 1. A method for identifying agents which disrupt binding complexes formed between salicylic acid (SA) or itsderivatives thereof and human high mobility group B1 (HsHMGB1) protein , comprisinga) providing a full length HsHMGB1 protein or protein fragments of them having SA binding sites in complex with SA or derivatives thereof,b) contacting said complex of step a) with said agent, andc) determining whether the agent of step b) displaces said SA or said SA derivative from said binding complex, agents which displace SA or said SA derivative being identified as analogs of SA which disrupt SA-HMGB1 binding complex formation, with the proviso that said agent is not glycyrrhizin.2. The method of performed in a cell free system.3. The method of claim 1 , performed in vitro.4. The method of claim 1 , wherein said SA derivative is selected from the group consisting of 4-azido SA and 3-aminoethyl SA.5. The method of claim 1 , wherein said agent is acetyl-3AESA or amorfrutin B1.6. The method of performed in vivo in a whole animal.7. The method of claim 3 , wherein said disruption is detected using ligand-detected NMR assays.8. The method of claim 3 , wherein said disruption is detected using protein-detected NMR assays.9. The method of claim 1 , performed in silico.10. The method of claim 9 , wherein said method is performed by virtual screening.11. The method of claim 5 , further comprising the step of measuring the effects of said agent on HsHMGB1 activity claim 5 , said activity being selected from the group consisting of DNA binding claim 5 , cytokine/chemokine—inducing activity claim 5 , chemo-attractant activity claim 5 , Cox-2-inducing activity claim 5 , induction of autophagy claim 5 , ...

Подробнее
03-03-2022 дата публикации

Enantiomerically enriched, polycrystalline molecular sieves

Номер: US20220062875A1

This disclosure describes enantiomerically enriched chiral molecular sieves and methods of making and using the same. In some embodiments, the molecular sieves are silicates or germanosilicates of STW topology.

Подробнее
25-02-2016 дата публикации

QUANTIFICATION OF IN VIVO METABOLITE

Номер: US20160051188A1

A magnetic resonance pulse sequence technique may acquire a water reference spectrum and two water suppressed metabolite spectra and with frequency selective inversion pulse centered at either single frequency, at multiple frequencies, or in a single acquisition. Subtraction of the inverted from non-inverted water suppressed metabolite spectrum results in single or a combination of specific metabolite peak/peaks alone with a flat baseline for easier quantification. 1. A method comprising:receiving a first measurement for spectra with selective inversion of a metabolite using magnetic resonance in a volume;receiving a second measurement for the metabolite without inversion using magnetic resonance in the volume; andquantifying the metabolite in the volume based on the difference of the first measurement and the second measurement.2. The method of claim 1 , wherein the magnetic resonance used is HMRS.3. The method of claim 1 , wherein the metabolite is glutamate/glutamine (Glx).4. The method of claim 1 , wherein the metabolite is creatine (Cr).5. The method of claim 1 , wherein the first measurement and the second measurement are done in vivo.6. The method of claim 1 , wherein the first measurement and the second measurement are done on a human brain.7. The method of claim 1 , further comprising monitoring a drug in a human based on the quantified metabolite.8. The method of claim 1 , further comprising determining efficacy of a drug based on the quantified metabolite.9. The method of claim 1 , further comprising determining aggressiveness of a tumor based on the quantified metabolite.10. A device comprising:a processor adapted to execute computer-readable instructions; and receiving a first measurement for a metabolite group inverted spectra using magnetic resonance in a volume;', 'receiving a second measurement for the metabolite group without inversion using magnetic resonance in the volume; and', 'quantifying the metabolite group in the area based on the ...

Подробнее
25-02-2021 дата публикации

MAGNETIC RESONANCE SPECTROSCOPY PULSE SEQUENCE, ACQUISITION, AND PROCESSING SYSTEM AND METHOD

Номер: US20210052185A1
Принадлежит:

Systems and methods are provided for processing a set of multiple serially acquired magnetic resonance spectroscopy (MRS) free induction decay (FID) frames from a multi-frame MRS acquisition series from a region of interest (ROI) in a subject, and for providing a post-processed MRS spectrum. Processing parameters are dynamically varied while measuring results to determine the optimal post-processed results. Spectral regions opposite water from chemical regions of interest are evaluated and used in at least one processing operation. Frequency shift error is estimated via spectral correlation between free induction decay (FID) frames and a reference spectrum. Multiple groups of FID frames within the acquired set are identified to different phases corresponding with a phase step cycle of the acquisition. Baseline correction is also performed via rank order filter (ROF) estimate and a polynomial fit. Sections of the ROF may be excluded from the polynomial fit, such as for example sections determined to be associated with relevant spectral peaks. 161.-. (canceled)62. A method for processing a set of multiple serially acquired magnetic resonance spectroscopy (MRS) free induction decay (FID) frames from a multi-frame MRS acquisition series from a region of interest (ROI) in a subject , and for providing a post-processed MRS spectrum , comprising a combination of at least two of the following:performing the step on the set at each of the multiple parameter values and providing multiple processed results, respectively, comprising multiple respective feature values, respectively, comparing the feature values of the processed results, determining a chosen feature value among the multiple feature values based upon the comparison and corresponding to a chosen parameter value, setting the parameter to the chosen parameter value for performing the processing step to provide the post-processed MRS spectrum;providing a first post-processed MRS spectrum, identifying a feature of a ...

Подробнее
23-02-2017 дата публикации

EXTERNAL STANDARD REFERENCE SYSTEM OF TYPE INSERTED INTO COIL OF HUMAN MAGNETIC RESONANCE IMAGING EQUIPMENT

Номер: US20170049354A1
Принадлежит:

The present invention relates to an external standard reference system of a type inserted into the coil of a human magnetic resonance imaging equipment, and more specifically, to a system capable of analyzing metabolic components (quantity of metabolites) in a human body without an error and a limited range using an external standard reference analysis method, in order to enhance accuracy of diagnosis by utilizing magnetic resonance spectroscopy of the human magnetic resonance imaging equipment. A system for evaluating performance of magnetic resonance spectroscopy includes an outer container for inserting an RF coil and provided with a plurality of holes; a plurality of inner containers arranged to be inserted into the plurality of holes respectively and capable of being filled with metabolites different from each other in at least a type or a concentration; and a frame for fixing a head of an object arranged inside the outer container. 1. A system for evaluating performance of magnetic resonance spectroscopy , the system comprising:an outer container for inserting an RF coil and provided with a plurality of holes;a plurality of inner containers arranged to be inserted into the plurality of holes respectively, the inner containers capable of being filled with metabolites that are different from each other in at least a type or a concentration; anda frame for fixing a head of an object arranged inside the outer container.2. The system according to claim 1 , wherein vertical lengths of at least some of the plurality of inner containers are different from each other.3. The system according to claim 1 , wherein the inner containers are filled with the metabolites.4. The system according to claim 3 , wherein the metabolites are different from each other in at least the type or the concentration.5. The system according to claim 3 , wherein the type and the concentration of at least some of the metabolites filled in the plurality of inner containers are replaceable.6. The ...

Подробнее
08-05-2014 дата публикации

IN VIVO QUANTIFICATION OF A VARIATION OF OXYGENATION IN A TISSUE BY USING A MAGNETIC RESONANCE IMAGING TECHNIQUE

Номер: US20140128720A1
Принадлежит:

The invention relates to a device and a method for quantifying a variation of oxygenation in a tissue by using a magnetic resonance imaging technique. The variation of oxygenation in a tissue can be quantified from a measured variation of a proton longitudinal relaxation rate ΔR1 and from calibration data. The method of the invention is characterized in that the variation of proton longitudinal relaxation rate ΔR1 that is used is a variation of proton longitudinal relaxation rate of lipids rather than a variation of proton longitudinal relaxation rate of water molecules. 210. Method according to further comprising between step a and step b a step of modifying an oxygen exposure of said tissue ().31010. Method according to wherein the step of modifying an oxygen exposure of said tissue () comprises an inhalation of an oxygen-enriched gas by a mammal body comprising said tissue ().41010. Method according to wherein the step of modifying an oxygen exposure of said tissue () comprises a placement of a tourniquet that allows a stricture of a part of a mammal body comprising said tissue ().5. Method according to claim wherein said sequence of radio-frequency pulses is able to remove a contribution of protons of water molecules to said proton longitudinal relaxation rate R1 of lipids.630. Method according to wherein said sequence of radio-frequency pulses comprises at least one saturation pulse () able to predominantly excite protons of water molecules.72040. Method according to wherein said sequence of radio-frequency pulses further comprises at least one initial inversion pulse () claim 6 , and at least one excitation pulse () of flip angle α.8. Method according to wherein said flip angle α has a value equal to or smaller than 30°.940. Method according to wherein said at least one excitation pulse () has a mean frequency and said mean frequency is shifted by a frequency shift below a resonance frequency of water molecules.10. Method according to wherein said frequency ...

Подробнее
14-02-2019 дата публикации

ATTENUATION CORRECTION IN EMISSION TOMOGRAPHY TAKING INTO ACCOUNT THE HARDWARE PARTS THAT ARE ACTUALLY PRESENT

Номер: US20190049539A1
Автор: Hugger Thimo, Junge Sven
Принадлежит:

A method to generate an attenuation correction map to compensate imaging errors in emission tomography resulting from the presence of hardware parts inside the imaging volume of an emission tomograph. Components of 3-dimensional CAD models of the hardware parts to be compensated are converted into voxels on a predetermined grid and assigned a filling factor per voxel. Image data sets of each component are multiplied with respective attenuation coefficients and thereafter superimposed to form an attenuation correction map. Thereby, in a simple and automatable way a profoundly exact, mostly noise-free and exactly reproducible attenuation correction map for attenuation correction in an emission tomography device may be generated. 1. A method for generating an attenuation correction map , to compensate imaging errors in emission tomograpy resulting from hardware parts present inside an imaging volume of an emission tomograph , comprising:(1.a) preparing or providing at least one 3-dimensional computer-aided design (CAD) model of the hardware parts being compensated;(1.b) converting required components of the CAD model into a 3-dimensional image data set into voxels on a predetermined grid and assigning a filling factor to each voxel;(1.c) pointwise multiplying the 3-dimensional image data set of each of the components with a respective known attenuation coefficient of the material that forms the respective component and a respective energy corresponding to an emission tomography radio tracer being used; and(1.d) super-imposing the 3-dimensional image data sets of all components of the hardware parts being compensated, to form at least one attenuation correction map.2. Method according to claim 1 , further comprising claim 1 , in an intermediate step claim 1 , triangulating the hardware parts in step (1.b).3. A method for performing a total attenuation correction of emission tomography image data sets with the attenuation correction map generated according to claim 1 , ...

Подробнее
14-02-2019 дата публикации

APPARATUS AND METHODS FOR DETERMINING PROPERTIES OF HYDROGEN-CONTAINING SAMPLES USING NUCLEAR MAGNETIC RESONANCE

Номер: US20190049617A1
Принадлежит:

Nuclear magnetic resonance (NMR) methods and apparatus are provided for investigating a sample utilizing NMR pulse sequences. In various embodiments, the NMR pulse sequences have a solid state portion and a line-narrowing portion. In other embodiments, the NMR pulse sequences have a first line-narrowing portion and a second line-narrowing portion where the sequences of the different portions are different. In yet other embodiments, the NMR pulse sequences have a Tportion and a line-narrowing portion. Processing of detected signals permits determination of characteristics of the sample including, in some cases, a differentiation of multiple components of the sample. 1. A nuclear magnetic resonance (NMR) tool , comprising:a magnet;a transmitter including a pulse sequencer and a power amplifier, wherein said pulse sequencer generates an NMR pulse sequence including a first portion comprising a solid state pulse sequence of a first type and a line-narrowing pulse sequence portion utilizing a repeated solid state pulse sequence of a second type different than said first type;a receiver including at least one antenna arranged to detect signals resulting from an interaction of said NMR field with a sample, including at least one first echo following said solid state pulse sequence portion and a plurality of second echoes between pulses of said line-narrowing pulse sequence portion; anda processor that processes said at least one first echo and said plurality of second echoes and determines an indication of a hydrogen content of the sample.2. The NMR tool of claim 1 , wherein said processor processes said first echo and said plurality of second echoes using an inverse Laplace transform.3. The NMR tool of claim 1 , wherein said NMR tool includes a body in which said magnetic claim 1 , said transmitter and said receiver are located and a cable coupled to said body.4. The NMR tool of claim 1 , wherein said first portion of said NMR pulse sequence comprises another line- ...

Подробнее
13-02-2020 дата публикации

METHODS AND SYSTEMS FOR ESTIMATING TRANSMIT ATTENUATION FOR A MAGNETIC RESONANCE IMAGING SCAN

Номер: US20200049786A1
Принадлежит:

Various methods and systems are provided for correcting transmit attenuation of an amplifier of a transmit radio frequency (RF) coil for use in a magnetic resonance imaging (MRI) system. In one example, a method includes setting a reference value of transmit attenuation for an amplifier of a transmit radio frequency (RF) coil, acquiring a two-dimensional Bfield map with the transmit attenuation set at the reference value, determining a mean flip angle from the Bfield map, determining a transmit attenuation correction value based on a prescribed flip angle and the mean flip angle, correcting the reference value of transmit attenuation with the transmit attenuation correction value to obtain a final value of transmit attenuation, and performing an MRI scan with the transmit attenuation set at the value. 1. A method for a magnetic resonance imaging (MRI) system , comprising:setting a reference value of transmit attenuation for an amplifier of a transmit radio frequency (RF) coil;{'sub': '1', 'acquiring a two-dimensional Bfield map with the transmit attenuation set at the reference value;'}{'sub': '1', 'determining a mean flip angle from the Bfield map;'}determining a transmit attenuation correction value based on a prescribed flip angle and the mean flip angle;correcting the reference value of transmit attenuation with the transmit attenuation correction value to obtain a final value of transmit attenuation; andperforming an MRI scan with the transmit attenuation set at the final value.2. The method of claim 1 , wherein acquiring the two-dimensional Bfield map comprises:acquiring a two-dimensional map of magnetic resonance (MR) signal phase shift during a pre-scan; and{'sub': 1', '1, 'deriving the two-dimensional Bfield map by converting the MR signal phase shift into corresponding Bfield strength.'}3. The method of claim 2 , wherein the map of MR signal phase shift is acquired by using Bloch-Siegert shift.4. The method of claim 1 , wherein the reference value of ...

Подробнее
23-02-2017 дата публикации

NUCLEAR MAGNETIC RESONANCE ANALYSIS METHOD

Номер: US20170052238A1
Автор: LE FUR Yann
Принадлежит:

Method for analyzing a sample including a species to be characterized and a reference species, includes: 130-. (canceled)31. A method for the spectroscopic analysis , using nuclear magnetic resonance (NMR) , of at least one sample comprising at least one species to be characterized and a reference species , the sample content of which is more than twice greater than the content of the at least one species to be characterized , with the method comprising the following steps:{'sub': '0', 'a. applying at least one constant field Bto the at least one sample,'}b. acquiring, using one or more antenna(s), one or more complex free induction decay (FID) signal(s) S(t), with each complex FID signal S(t) comprising a real part and an imaginary part; with the sample being such that the relative content of the reference species and of the at least one species to be characterized, as well as the relative relaxation times thereof result in that, in the at least one complex FID signal S(t), the amplitude of the signal of the reference species is at least twice greater than the amplitude of the signal of the at least one species to be characterized,wherein the method also comprises at least the following steps of:{'sub': 0Ref', '0Ref, 'c. obtaining a FID spectrum S(ω) by applying a Fourier transform to the real and complex parts of the at least one complex FID signal S(t), with the FID spectrum S(ω) obtained then comprising the reference species and the species to be characterized and having two portions (UFR, DFR), each extending from the resonance frequency of the reference species Fand respectively on either side of F, with a resonance frequency of the species to be characterized being located on a first portion of the spectrum taken among said two portions (UFR, DFR);'}d. modeling the signal of the reference species Sref(t) from the real and complex parts of the at least one complex FID signal S(t);{'sub': 0Ref', 'ORef, 'e. obtaining a spectrum Sref(ω) of the reference species ...

Подробнее
26-02-2015 дата публикации

System and Method for Processing NMR Signals

Номер: US20150057979A1
Принадлежит: Jeol Ltd

There is disclosed an NMR signal processing method for accurately estimating the intensities of p peaks of interest in an NMR spectrum by the use of a mathematical model that represents a time-domain, free induction decay (FID) signal obtained by an NMR measurement as a sum of q signal components. First, q parameters (each being a combination of a pole and a complex intensity) defining q signal components are estimated for each value of the estimation order q of the mathematical model while varying the value of the estimation order q (S 34 ). At each value of the estimation order q, p parameters are selected from the q parameters in accordance with selection criteria (S 42 , S 46 ). The selected p parameters are evaluated (S 48 ). An optimal value of the estimation order is determined based on the evaluation values produced at the various values of the estimation order q, and p parameters corresponding to the optimal value of the estimation order is identified. The intensities of p peaks of interest are found from the identified p parameters.

Подробнее
22-02-2018 дата публикации

STRIPLINE DETECTOR FOR IN SITU BATTERY AND FUEL CELL NMR

Номер: US20180053973A1
Принадлежит:

Provided are batteries and fuel cells incorporating a stripline detector for use in nuclear magnetic resonance (NMR). The stripline batteries and fuel cells can be used for in situ NMR measurement of battery or fuel cell chemistry. Also provided are methods for measuring in situ battery and fuel cell NMR using the stripline batteries and fuel cells of the invention. 1. A battery comprising a stripline detector.2. The battery of claim 1 , further comprising metallic cathode and anode support plates arranged in substantially parallel planes and situated on opposite sides of the stripline detector.3. The battery of claim 2 , wherein the metallic cathode support plate comprises aluminum.4. The battery of claim 2 , wherein the metallic cathode support plate further comprises a cathode material deposited on the cathode support plate.5. The battery of claim 4 , wherein the cathode material deposited on the cathode support plate is selected from the group consisting of lithium iron phosphate (LiFePO) claim 4 , lithium cobalt oxide (LiCoO) claim 4 , and spinel cathode materials.6. The battery of claim 2 , wherein the metallic anode support plate comprises copper.7. The battery of claim 6 , wherein the metallic anode support plate further comprises an anode material deposited on the anode support plate.8. The battery of claim 7 , wherein the anode material deposited on the anode support plate is graphite.9. The battery of claim 2 , further comprising a first nonconductive separator situated between the stripline detector and the metallic cathode support plate claim 2 , and a second nonconductive separator situated between the stripline detector and the metallic anode support plate claim 2 , wherein the first nonconductive separator electrically isolates the stripline detector from the cathode claim 2 , and the second nonconductive separator electrically isolates the stripline detector from the anode.10. The battery of claim 9 , wherein the first nonconductive separator and ...

Подробнее
10-03-2022 дата публикации

Magnetic resonance imaging drug containing a deuterated natural branched-chain amino acid, and diagnostic method using said drug

Номер: US20220072162A1
Принадлежит: Solvex Solvex LLC

The invention relates to the means for magnetic resonance imaging of oncological diseases and other diseases, accompanied by a locally altered level of absorption of nutrients by cells. The invention is the diagnostic drug containing at least one deuterated derivative of a natural branched-chain amino acid, as well as the diagnostic method based on the use of this diagnostic drug. The method of the invention includes performing magnetic resonance imaging and/or deuterium magnetic resonance spectroscopy after administration of the diagnostic drug in a time sufficient for the accumulation of the diagnostic drug in a target area of a subject's body. The proposed method allows to carry out a highly informative diagnostics of oncological diseases and other diseases, accompanied by a locally altered level of absorption of nutrients by cells.

Подробнее
13-02-2020 дата публикации

Method for Characterizing a Sample by Data Analysis

Номер: US20200051669A1
Принадлежит:

A method for characterizing a sample is disclosed, having the following steps: providing at least one analysis result having a plurality of values, wherein the analysis result was generated by the analysis of a sample by at least one analysis method; determining the value of at least one mathematic relation between at least two values of the plurality of values; generating a characterizing signature of the sample on the basis of the value of the at least one mathematic relation. Furthermore, a method for characterizing a system is disclosed in which method the preceding method is used. 1. A method for characterizing a system , comprising the following steps:providing a first analysis result having a plurality of values, wherein the first analysis result was generated by an analysis of a first sample taken from a system by an analysis method chosen from a group consisting of NMR spectroscopy, mass spectrometry, electron spin resonance, vibrational spectroscopy, UV/VIS spectroscopy, and fluorescence spectroscopy;determining a first set of values of a quotient between pairs of two values of a first plurality of values; a) determining a first deviation between the first set of values of the quotient and a first average correlation matrix that has been obtained by summing up a plurality of a second set of values of a quotient, wherein the second set of values of the quotient has been obtained by providing a second analysis result having a second plurality of values, wherein the second analysis result method is the same analysis used for the first analysis result, and determining the second set of values of a quotient between the first set of values;', 'b) determining a second deviation between the first set of values of the quotient and a second average correlation matrix that has been obtained by summing up a plurality of a third set of values of a quotient, wherein the third set of values of the quotient has been obtained by providing a third analysis result having a ...

Подробнее
01-03-2018 дата публикации

ORGANOMETALLIC COMPOUND

Номер: US20180055810A1
Принадлежит:

The present patent application relates to a novel organometallic compound, a process for the preparation thereof, and its use. 116.-. (canceled)18. A method for the preparation of the compound according to claim 17 , comprising:a) providing a specific amount of a cis-diamminedihalide Pt (II) complex in an aqueous solution;b) conversion of this cis-diamminedihalide Pt (II) complex with the 1.8- to 2.2-fold molar amount (with respect to the cis-diamminedihalide Pt (II) complex) of silver-p-toluenesulfonate at a temperature of less than 100° C. while stirring;c) optional addition of alkaline or alkaline earth halide to precipitate excess silver ions;d) simple or multiple filtration for the separation of insoluble silver halides;e) precipitation of the reaction product;f) filtration of the reaction product in order to obtain a solid reaction product and the filtrate, and an optional washing of the reaction product.19. The method according to claim 18 , wherein the precipitation in step e) is accomplished by the distilling off water under reduced pressure at a temperature below 50° C. claim 18 , by addition of a precipitant or combinations thereof.20. The method according to claim 19 , wherein about 75% to about 65% of the water is distilled off.21. The method according to claim 19 , wherein the precipitant is an organic solvent claim 19 , in particular ethanol or acetone.22. The method according to claim 18 , wherein step c) includes a precipitation step for the precipitation of excess alkaline earth ions.23. The method according to claim 18 , wherein the silver-p-toluenesulfonate is used in the doubled molar amount vis-à-vis cis-diamminedihalide Pt (II) complex.24. The method according to claim 18 , including the additional step g) claim 18 , in which the filtrate is cooled to a temperature between 0° C. and 10° C. claim 18 , and the precipitated reaction product is filtered off.25. The method according to claim 18 , wherein claim 18 , in step e) claim 18 , the pH ...

Подробнее