Reader Devices for Optical and Electrochemical Test Devices

This invention relates generally to devices and methods for performing optical and electrochemical assays and, more particularly, to devices having optical and electrochemical detectors and to methods of performing optical and electrochemical assays using such devices. The present invention is particularly useful for performing immunoassays and/or electrochemical assays at the point-of-care.

Microscope and method for observing biological specimen in living state

A biological specimen containing a chemiluminescence substance that generates chemiluminescence is observed in a living state under a microscope. The microscope includes a light source that outputs control light that changes the state of the chemiluminescence, a defining unit that defines the radiation pattern of the control light with which an observation surface of the biological specimen is irradiated, and a detector that detects the chemiluminescence from the biological specimen.

TEST INSTRUMENT AND METHOD OF CONTROLLING THE SAME

Disclosed herein are a test instrument and a method of controlling the same, capable of performing a basic test on a sample of a patient, determining whether to perform an additional test, and displaying interfaces associated with a progress level, a necessary time, etc. of the additional test on a display unit when the additional test is performed, thereby enabling a user to visibly recognize information associated with a performing process of each test. The test instrument includes: a detection unit configured to apply light to at least one chamber in which a reaction between a reagent and a sample occurs and to detect an optical signal from the chamber to test the sample held in a reaction device, a control unit configured to determine whether to perform a secondary test on the sample after a primary test is performed on the sample and to control to display a secondary test progress interface showing a progress level of the secondary test when the secondary test is performed, and a display unit configured to display a primary test progress interface showing a progress level of the primary test on the sample and to display the secondary test progress interface showing the progress level of the secondary test when the secondary test is performed on the sample. 1. A test instrument comprising:a detection unit configured to apply light to at least one chamber in which a reaction between a reagent and a sample occurs and to detect an optical signal from the chamber to test the sample held in a reaction device;a control unit configured to determine whether to perform a secondary test on the sample after a primary test is performed on the sample and to control to display a secondary test progress interface showing a progress level of the secondary test when the secondary test is performed; anda display unit configured to display a primary test progress interface showing a progress level of the primary test on the sample and to display the secondary test progress ...

TESTING TOXICITY OF A TEST SAMPLE

Invention describes a method and a device for testing toxicity of a test sample. The method comprises at least the steps of: providing an aliquot or a volume of light producing test reagent liquid in a reagent vial, moistening a control swab with the light producing test reagent liquid, moistening a test swab with the test sample, moistening the test swab with the light producing test reagent liquid, reading luminescence of the control swab in a luminometer and thereby obtaining a luminescence value of a control sample, reading luminescence of the test swab in the luminometer and obtaining a luminescence value of the test sample, calculating the toxicity of the test sample by comparing the luminescence value of the control sample to the luminescence value of the test sample. According to the invention the moistenings of the control swab and the test swab with the light producing test reagent liquid are done with the same aliquot of light producing test reagent liquid in the same reagent vial.” 2. The method according to claim 1 , whereinthe test sample and the aliquot of light producing test reagent liquid are mixed together, thereby producing a mixture, and thereafterthe test swab is moistened with the test sample and with the light producing test reagent liquid by moistening the test swab in said mixture.3. The method according to claim 1 , whereinthe aliquot of light producing test reagent liquid in the reagent vial is provided by reconstituting a light producing test reagent with reconstitution liquid in the reagent vial.4. The method according to claim 3 , wherein the light producing test reagent is reconstituted by puncturing a reconstitution liquid chamber with the control swab claim 3 , thereby arranging the reconstitution liquid to mix with the light producing test reagent in the reagent vial.6. The method according claim 5 , wherein the control swab and the test swab are moved inside the elongated device body in their own separate tubes keeping the swabs ...

Plasma-processing detection indicator in which metal oxide fine particles are used as color-change layer

The present invention provides a plasma treatment detection indicator including a color-changing layer that changes color by plasma treatment, exhibiting excellent heat resistance, with the gasification of the color-changing layer or the scattering of the fine debris of the color-changing layer caused by the plasma treatment being suppressed to the extent that electronic device properties are not affected. Specifically, the present invention provides a plasma treatment detection indicator comprising a color-changing layer that changes color by plasma treatment, the color-changing layer comprising metal oxide fine particles containing at least one element selected from the group consisting of Mo, W, Sn, V, Ce, Te, and Bi, the metal oxide fine particles having a mean particle size of 50 μm or less.

Method and apparatus for measuring enzyme activity

Ink composition for plasma processing detection, and indicator for plasma processing detection using said ink composition

The present invention provides an ink composition for forming a color-changing layer that changes color by plasma treatment, the ink composition exhibiting excellent heat resistance, with the gasification of the color-changing layer or the scattering of the fine debris of the color-changing layer caused by plasma treatment being suppressed to the extent that electronic device properties are not affected. The invention provides an ink composition for forming a color-changing layer that changes color by plasma treatment, the ink composition comprising metal oxide particles containing at least one element selected from the group consisting of Mo, W, Sn, V, Ce, Te, and Bi, and a binder resin.

Reader devices for optical and electrochemical test devices

This invention relates generally to devices and methods for performing optical and electrochemical assays and, more particularly, to devices having optical and electrochemical detectors and to methods of performing optical and electrochemical assays using such devices. The present invention is particularly useful for performing immunoassays and/or electrochemical assays at the point-of-care.

In vivo screening array

The invention features methods of evaluating the effect of a plurality of different treatments or compounds on a tissue. The method includes providing a tissue from an animal; contacting the tissue with a plurality of treatment, forming on the tissue an array of a plurality of regions or addresses. The method includes the use of a two dimensional array member to contact the plurality of treatments with the tissue and/or to evaluate their effect. The methods are useful for screening large numbers of therapeutic or cosmetic compounds.

Ink composition for plasma processing detection, and indicator for plasma processing detection using said ink composition

（課題）プラズマ処理により変色する変色層を形成するためのインキ組成物であって、プラズマ処理により変色層がガス化したり微細な屑となって飛散したりすることが、電子デバイス特性に影響を及ぼさない程度に抑制されており、且つ、耐熱性が良好なプラズマ処理検知インキ組成物を提供する。 （解決手段）プラズマ処理により変色する変色層を形成するためのインキ組成物であって、Mo、W、Sn、V、Ce、Te及びBiからなる群から選択される少なくとも一種の元素を含む金属酸化物粒子並びにバインダー樹脂を含有することを特徴とするプラズマ処理検知インキ組成物。

Method for detecting crack position in diamond compact

本发明公开了一种检测金刚石复合片内部裂纹位置的方法，所述金刚石复合片包括聚晶金刚石和金刚石复合片基体，所述金刚石复合片基体中含有钴，将所述金刚石复合片完全浸泡在浓度为0.001g/L～120g/L的铜盐溶液中，浸泡30秒至5小时后取出，用水简单地轻微冲洗。本发明方法不仅可以检测出金刚石复合片内部是否存在裂纹，并且可以准确检测出内部裂纹的位置。本发明方法对金刚石复合片几乎无损伤，检测之后的金刚石复合片可以像检测之前一样继续使用，并且操作简单、方便快速、准确性高、重复性好。

Monitering Method of Metal Impurity of Chemical Solution in Semiconductor Process

The present invention relates to an online monitoring method for quantitatively detecting metal, contained in at least two chemical solutions used for a semiconductor process, by using an external calibration curve which is the detection sensitivity of detecting equipment in accordance with metal concentration of each detection target metal. More specifically, the method includes the steps of: (a) selecting a first metal group, quantified with the external calibration curve, and a second metal group, using the external calibration curve but requiring correction, from detection target metal groups; (b) obtaining the external calibration curve for each detection target metal; (c) measuring sensitivity for each detection target metal and internal standard elements by injecting the internal standard elements into each of the chemical solutions for the semiconductor process at predetermined concentration and divisionally supplying the solutions to the detecting equipment; and (d) quantifying the detection target metal, contained in the chemical solutions, with the external calibration curve if the detection target metal belongs to the first metal group, and quantifying the detection target metal, contained in the chemical solutions, by using the external calibration curve and the sensitivity of the detection target metal, corrected with the sensitivity of the internal standard elements measured at the step (c), if the detection target metal belongs to the second metal group.

Detection of analytes using nanoparticles as light scattering enhancers

A method for detecting the presence of an analyte (1) in a solution (2) comprising: providing at least a first and a second probes (A, B) different from each other, each probe (A,B) comprising a nanoparticle conjugated with a receptor specific to the analyte (1); contacting the solution (2) suspected of including the analyte (1) with the first and the second probes (A, B) to form a sample solution (3), wherein the sample solution (3) comprises aggregates (4) comprising the analyte (1) combined with the first and the second probes (A, B); illuminating the sample solution (3) with a light source having at least a first and a second exciting wavelengths (?eA, ?eB) different from each other wherein the first and the second wavelength are chosen to get specific optical responses from the first probe (A) and the second probe (B) respectively when illuminated; detecting as a function of time the light scattered by the first probe (A) at a first detection wavelength (?dA) and the light scattered by the second probe (B) at a second detection wavelength (?dB) to get a first signal and a second signal respectively; and detecting temporal coincidences between said first signal and second signal.

Method for detecting location of probe bead in capillary bead array

It is an object to provide a method for accurately identifying the order of probe beads, namely, the types of probes bound to the probe beads, by readily and precisely detecting the locations of all the beads in a capillary bead array using a fluorescence reading apparatus. It is also an object to significantly improve the reliability of results of biochemical or immunological inspection in which a capillary bead array is used. Probe beads 102 are arranged in a capillary 101 . A solution that includes fluorescence-labeled target biomolecules is introduced into the capillary 101 . A fluorescence image that includes the fluorescence spot 108 of a probe bead 105 that captured the biomolecules is obtained by the fluorescence reading apparatus. A solution that includes fluorescent material for staining all the beads is introduced into the capillary 101 . A fluorescence image that includes the fluorescence spot area 114 of all the probe beads 113 is obtained by the fluorescence reading apparatus. The location and the order of the probe bead 105 that has captured the biomolecules is accurately determined by overlaying the fluorescence image that includes the fluorescence spot 108 of the probe bead that has captured the biomolecules and the fluorescence image that includes the fluorescence spot area 114 of all the probe beads 113.

하이드로겔을 이용한 표적 분석물질의 검출방법 및 이를 이용한 바이오 센싱 장치

본 발명은 하이드로겔을 이용한 표적 분석물질의 검출방법 및 이를 이용한 바이오센싱 장치에 관한 것으로서, 구체적으로 고분자 하이드로겔에 고정된 표적 분석물질 프로브가 표적 분석물질과 결합하여 하이드로겔의 부피 변화를 유도하면 모이레 패턴의 변화 발생을 통한 표적 분석물질의 감지 및 농도 정량이 용이하게 이루어질 수 있는 검출방법 및 장치를 제공한다.

检测脂多糖的比色传感器、其制备方法和应用

本发明公开了一种检测脂多糖的比色传感器、其制备方法和应用，传感器通过紫外‑可见光谱技术进行检测，其特征在于利用了氨基苯硼酸修饰的磁纳米颗粒对脂多糖的识别及其类似于过氧化物酶的催化氧化活性和脂多糖类脂质双层对离子运输的阻碍作用。本发明利用了3‑氨基苯硼酸与脂多糖的高特异性结合及脂多糖类脂质双层对离子运输的阻碍作用，保证了检测的高度特异性，借助磁纳米颗粒类似于过氧化物酶的催化氧化活性，提高了检测的灵敏性。通过紫外‑可见光谱技术捕捉磁纳米催化H 2 O 2 氧化ABTS产生的颜色变化，实现了脂多糖的分析检测。本发明方法简单、快速、无需信号标记；灵敏度高，可以在0.00001 μg/mL到180 μg/mL范围内线性检测脂多糖；特异性强，可以有效地区分脂多糖与其他对照物质。

生物传感器及其制备方法

本发明公开了一种生物传感器及其制备方法，包括：集成光源，该光源被配置为产生光学信号；滤波单元，包括环形谐振单元，该滤波单元被配置为接收输入光源信号并产生带宽较窄的检测输入光学信号；传感单元，包括环形谐振器阵列，该传感单元被配置为接收输入光学信号并产生传感光学信号，该传感光学信号的波长和光强会根据检测物质材料的浓度等信息而发生变化；检测单元，所述的检测单元用于根据输出传感光学信号分析得到所测混合物中各物质成分的存在及浓度信息。

生体試料を生存状態で観察する顕微鏡および方法

化学発光を生成する化学発光物質を含む生体試料を生存状態で顕微鏡により観察する。前記顕微鏡は、前記化学発光の状態を変化させる制御光を射出する光源と、前記生体試料の観察面に照射される前記制御光の照射パターンを画定する画定部と、前記生体試料から射出された前記化学発光を検出する検出器と、を備える。

一种高温净气除一氧化碳催化剂的制作方法

本发明公开了一种高温净气除一氧化碳催化剂的制作方法，涉及催化剂制造技术领域；本发明包括S1、载体加工：将催化剂载体放置于加工装置内部进行加工，使用钻孔装置对催化剂载体表面进行钻孔，从而钻出多个贯穿孔，并在钻孔完成后，使用疏通排杂装置将贯穿孔内部残留的催化剂载体废料粉末排出；S2、催化剂原料制作：将Pd、Pt等金属混合，并通过细化装置加工为纳米级材料，同时在加工过程中将催化剂原料内部的杂质剔除。本发明通过对催化剂原料进行耐高温检测可以在催化剂生产初期对催化剂原料质量进行判断，从而在催化剂原料品质较差的情况下减少后续加工操作，不仅可以提高良品率，还可以降低加工成本。

Microscope and method for observing biological sample in living state

高灵敏度生物传感器及其制备方法

本发明公开了一种高灵敏度生物传感器及其制备方法，包括：集成光源，该光源被配置为产生光学信号；滤波单元，包括环形谐振单元，该滤波单元被配置为接收输入光源信号并产生带宽较窄的检测输入光学信号；传感单元，包括环形阵列及马赫‑曾德尔干涉仪阵列，该传感单元被配置为接收输入光学信号并产生传感光学信号，该传感光学信号的波长和光强会根据检测物质材料的浓度等信息而发生变化；检测单元，所述的检测单元用于根据输出传感光学信号分析得到所测混合物中各物质成分的存在及浓度信息。

生体試料を生存状態で観察する顕微鏡および方法

化学発光を生成する化学発光物質を含む生体試料を生存状態で顕微鏡により観察する。前記顕微鏡は、前記化学発光の状態を変化させる制御光を射出する光源と、前記生体試料の観察面に照射される前記制御光の照射パターンを画定する画定部と、前記生体試料から射出された前記化学発光を検出する検出器と、を備える。

감광활성 측정 제제, 및 이를 이용한 키트 및 방법

포르마잔을 포함하는 감광활성 측정 제제는, 감광성 화합물과 직접적으로 반응하여 신속하고 간편하게 감광활성을 측정할 수 있다. 상기 감광활성 측정 제제는, 다양한 구성의 측정 키트 또는 방법에 적용되어, 각종 감광성 화합물의 추적과 감광성 화합물의 화학 반응에 관련된 광범위한 연구 및 산업적 활용을 가능하게 한다.

光谱分析装置

本发明公开了一种光谱分析装置。该可见光光谱分析装置包括壳体组件、机芯组件以及光电组件；机芯组件设在壳体组件内,机芯组件具有电源部件；光电组件设于壳体组件内，光电组件包括纳米试剂加热模块、光信号接收部件、光信号发射部件、温度检测部件以及致冷部件，纳米试剂加热模块具有用于供PCR管放置的反应槽以及贯穿纳米试剂加热模块且与反应槽连通的检测通孔，光信号发射部件设置于检测通孔的一端开口处，光信号接收部件设置于检测通孔的另一端开口处；温度检测部件用于检测括纳米试剂加热模块的温度，电源部件与纳米试剂加热模块、光信号接收部件、光信号发射部件以及温度检测部件电性连接。该可见光光谱分析装置体积小、成本低。

Sistema de cartucho interferometrico y metodos relacionados.

Se proporciona un sistema de cartucho de interferómetro de guía de onda óptica y métodos relacionados. El sistema de cartucho de interferómetro de guía de onda óptica incluye una carcasa de cartucho que comprende un chip interferométrico y una oblea de celda de flujo, así como un medio de alineación para alinear el sistema de cartucho dentro del sistema interferométrico.

Interferometric cartridge system and related methods

An optical waveguide interferometer cartridge system and related methods are provided. The optical waveguide interferometer cartridge system includes a cartridge housing comprising an interferometric chip and a flow cell wafer as well as an alignment means for aligning the cartridge system within the interferometric system.

시료의 성능평가장치가 구비된 플라즈마중합 연속처리장치

본 발명은 시료의 성능평가장치가 구비된 플라즈마중합 연속처리장치에 관한 것으로서, 본 발명에 의하면 자외선분광계를 이용한 시료의 성능평가장치가 구비된 플라즈마중합 연속처리장치를 제공하여 시료의 성능평가 중에 시료에 손상을 주지 않으면서 연속적으로 시료의 성능평가를 수행할 수 있어, 플라즈마중합처리 후 시료의 불량판별 및 신속한 조치를 용이하게 할 수 있다.

Method and system for inspecting growth quality of graphene

Provided is a method of inspecting a growth quality of a graphene layer of a graphene-grown copper foil obtained by growing the graphene layer on a copper foil layer by chemical vapor deposition (CVD), the method including reacting oxygen or water molecules with the copper foil layer via a defect portion of the graphene layer, partitioning an entire region of the graphene-grown copper foil into partial regions, sequentially obtaining images of the partial regions, detecting, with respect to each of the images of the partial regions, an oxidized region where the copper foil layer is oxidized, and setting the oxidized region as a graphene defect region, and obtaining a ratio of an area of the graphene defect region to an entire area of each of the images of the partial regions.

Camouflaging on chip, methods, and systems and its use for testing biological and non-biological analytes

An apparatus for detection of an analyte includes a first detectable agent having one or more detectable characteristic and masking agent having one or more characteristic that masks the detection of the one or more characteristic of the first detectable agent in absence of the analyte, wherein at least one of the first detectable agent or the masking agent is configurable in the presence of the analyte to allow detection of the one or more characteristic of the first detectable agent which is indicative of the presence of the analyte.

Uv/h2o2降解水中典型有机物反应速率常数的测定方法

本发明公开了一种实际水中UV/H 2 O 2 降解典型有机物反应速率常数的测定方法，包括：(1)采用配套UV/H 2 O 2 高级氧化装置开展静态实验；(2)配套UV/H 2 O 2 高级氧化装置，为静态实验装置；(3)实际水中UV/H 2 O 2 降解UV 254 的一级反应动力学常数测定；(4)实际水中UV 254 降解的二级反应动力学常数测定；(5)竞争动力学模型；(6)实际水中UV 254 和典型有机物C的一级反应动力学常数测定r UV 和r；(7)典型有机物的二级反应动力学常数测定。本发明量化了实际水中NOM、无机离子等对典型痕量有机物的降解速率影响，为UV/H 2 O 2 高级氧化工艺实际应用提供了理论支持和工艺参数设计依据。

一种高温净气除一氧化碳催化剂的制作方法

本发明公开了一种高温净气除一氧化碳催化剂的制作方法，涉及催化剂制造技术领域；本发明包括S1、载体加工：将催化剂载体放置于加工装置内部进行加工，使用钻孔装置对催化剂载体表面进行钻孔，从而钻出多个贯穿孔，并在钻孔完成后，使用疏通排杂装置将贯穿孔内部残留的催化剂载体废料粉末排出；S2、催化剂原料制作：将Pd、Pt等金属混合，并通过细化装置加工为纳米级材料，同时在加工过程中将催化剂原料内部的杂质剔除。本发明通过对催化剂原料进行耐高温检测可以在催化剂生产初期对催化剂原料质量进行判断，从而在催化剂原料品质较差的情况下减少后续加工操作，不仅可以提高良品率，还可以降低加工成本。

一种靶向药物药敏检测装置

本发明公开了一种靶向药物药敏检测装置，包括放置机构，放置机构包括箱体，所述箱体内固定连接有固定板，所述固定板的上端固定连接有多块隔板，多块所述隔板将箱体内部分隔成多个单独空间，多个所述单独空间内均设有滑板，所述滑板与固定板滑动连接，所述固定板内设有用于对多块固定板进行移动的移动机构，所述箱体的前端铰接有多个箱门，多个所述箱门与多个单独空间相匹配，所述滑板的上方放置有培养皿，所述滑板上设有用于对培养皿进行固定的固定机构。本发明对培养皿的放置稳定且对药物检测时具有对比性，对药敏检测效果较好，检测效率高。

光谱分析装置

本发明公开了一种光谱分析装置。该可见光光谱分析装置包括壳体组件、机芯组件以及光电组件；机芯组件设在壳体组件内,机芯组件具有电源部件；光电组件设于壳体组件内，光电组件包括纳米试剂加热模块、光信号接收部件、光信号发射部件、温度检测部件以及致冷部件，纳米试剂加热模块具有用于供PCR管放置的反应槽以及贯穿纳米试剂加热模块且与反应槽连通的检测通孔，光信号发射部件设置于检测通孔的一端开口处，光信号接收部件设置于检测通孔的另一端开口处；温度检测部件用于检测括纳米试剂加热模块的温度，电源部件与纳米试剂加热模块、光信号接收部件、光信号发射部件以及温度检测部件电性连接。该可见光光谱分析装置体积小、成本低。

광화학 반응 감지 장치

본 발명은 광화학 반응 감지 장치에 관한 것으로, 본 발명의 일면에 따른 광화학 반응 감지 장치는 광화학 반응에 따라 화학중합체 코팅 기판에서 발광된 빛의 세기를 감지함에 따라 각 시점의 센싱값으로 구성된 광검출데이터를 출력하는 광학 검출기 및 광학 검출기로부터 입력된 광검출데이터를 이용해 광화학 반응 여부를 판단하는 제어모듈을 포함하고, 제어모듈은 광학 검출기에서 감지된 센싱값으로 구성된 각 시점에 대한 광검출데이터를 입력받아 기설정된 시간에 따른 샘플링 시점마다 시간 동안 입력된 광검출데이터의 중간값을 산출하고, 초기 샘플링 시점의 중간값과 기설정된 초기값을 가중합해서 1차 필터링값을 산출한 후 직전에 산출된 1차 필터링값을 이용해 각 샘플링 시점의 중간값과 직전에 산출된 1차 필터링값을 가중합하여 각 샘플링 시점의 1차 필터링값을 산출하며, 초기 샘플링 시점의 1차 필터링값과 기설정된 초기값을 가중합해서 2차 필터링값을 산출한 후 직전에 산출된 2차 필터링값을 이용해 각 샘플링 시점의 1차 필터링값과 직전에 산출된 2차 필터링값을 가중합하여 각 샘플링 시점의 2차 필터링값을 산출하고, 각 샘플링 시점의 2차 필터링값에 따라 광화학 반응 여부를 판단한다.

一种靶向药物药敏检测装置

本发明公开了一种靶向药物药敏检测装置，包括放置机构，放置机构包括箱体，所述箱体内固定连接有固定板，所述固定板的上端固定连接有多块隔板，多块所述隔板将箱体内部分隔成多个单独空间，多个所述单独空间内均设有滑板，所述滑板与固定板滑动连接，所述固定板内设有用于对多块固定板进行移动的移动机构，所述箱体的前端铰接有多个箱门，多个所述箱门与多个单独空间相匹配，所述滑板的上方放置有培养皿，所述滑板上设有用于对培养皿进行固定的固定机构。本发明对培养皿的放置稳定且对药物检测时具有对比性，对药敏检测效果较好，检测效率高。

高灵敏度生物传感器及其制备方法

本发明公开了一种高灵敏度生物传感器及其制备方法，包括：集成光源，该光源被配置为产生光学信号；滤波单元，包括环形谐振单元，该滤波单元被配置为接收输入光源信号并产生带宽较窄的检测输入光学信号；传感单元，包括环形阵列及马赫‑曾德尔干涉仪阵列，该传感单元被配置为接收输入光学信号并产生传感光学信号，该传感光学信号的波长和光强会根据检测物质材料的浓度等信息而发生变化；检测单元，所述的检测单元用于根据输出传感光学信号分析得到所测混合物中各物质成分的存在及浓度信息。

生物传感器及其制备方法

本发明公开了一种生物传感器及其制备方法，包括：集成光源，该光源被配置为产生光学信号；滤波单元，包括环形谐振单元，该滤波单元被配置为接收输入光源信号并产生带宽较窄的检测输入光学信号；传感单元，包括环形谐振器阵列，该传感单元被配置为接收输入光学信号并产生传感光学信号，该传感光学信号的波长和光强会根据检测物质材料的浓度等信息而发生变化；检测单元，所述的检测单元用于根据输出传感光学信号分析得到所测混合物中各物质成分的存在及浓度信息。

定性检测方法、服务器及具有存储功能的装置

本发明公开了一种定性检测方法、服务器及具有存储功能的装置，该方法包括：接收来自便携式终端拍照获得的包括待检测对象和空白参照对象的图片，获取并分析图片上待检测对象和空白参照对象所分别对应的RGB数据；根据待检测对象的RGB数据的量值大小和空白参照对象的RGB数据的量值大小以及预设判定策略，确定待检测对象对应的待检测物质含量的检测结果为阳性还是阴性。通过上述方式，本发明能够实现物质简单、快速及客观的定性检测。

Reader devices for optical and electrochemical test devices

This invention relates generally to devices and methods for performing optical and electrochemical assays and, more particularly, to devices having optical and electrochemical detectors and to methods of performing optical and electrochemical assays using such devices. The present invention is particularly useful for performing immunoassays and/or electrochemical assays at the point-of-care.