Method for preparing levogyrate amlodipine of maleic acid and combination of medication of conataining it

A laevo-amlodipine maleate used to prepare the medicines for treating hypertension and angina pectoris, its preparing process and said medicines are disclosed.

Red sage root ligustrazine freeze dried injecta and preparation method thereof

The invention provides a red sage root ligustrazine freeze dried injecta and its preparation, wherein the injection is in powder form, and comprises red sage root extract, Chuangxiongzine Hydrochlorid and right amount of filling agent by the weight proportion of 400-1100:50-150:0-200, the preparing process comprises extracting red sage root liquid, configuring the soup, freeze drying and packaging.

Pharmaceutical composition for treating chronic stable angina pectoris with hyperlipemia

The invention relates to a pharmaceutical composition for treating chronic stable angina pectoris with hyperlipermia, which comprises the components of a drug carrier, a sino atrial node If current selective specificity inhibitor or pharmaceutical salt thereof, and an HMG-CoA reductase selective depressant or pharmaceutical salt thereof; the sino atrial node If current selective specificity inhibitor or the pharmaceutical salt thereof is Ivabradine hydrochloride; and the contents of the components of the medical composition by mass unit are 2.5 to 10 of the sino atrial node If current selective specificity inhibitor and 2.5 to 100 of the HMG-CoA reductase selective depressant. The medical composition has good synergistic effect when treating the chronic stable angina pectoris with the hyperlipermia, and has good effect of lowering hyperlipemia for hyperlipoidemia and hemorheology effect.

Oxiracetam preparation and method of preparing the same

The invention provides an oxiracetam agent and the preparation method, which relates to medical technical field and is used to induce the drug to penetrate through blood-brain barrier and to improve treatment effects. The agent contains oxiracetam nano-particle and excipientpharmaceutical excipient. After improved, the oxiracetam nano-particle and excipientpharmaceutical excipient contains drug core and a modified layer. The drug core mainly comprises principal agent and carrier, wherein the carrier is polymer material containing amino polysaccharide with a content of 70 to 95 percent, and theprincipal agent is oxiracetam with a content of 5 to 30 percent. The invention adopts polymer material containing amino polysaccharide as carrier to carry the oxiracetam and endow the oxiracetam withgood brain targeting function. And the invention adopts surfactant to modify the nano surface of the carrier and lengthens the recycling time of the carrier nano-granule and the nano-particle in therecycling ...

Soft capsule of atovastatine salts and prepn. method therefor

Anti-cold medicine soft capsule and its preparing method

The present invention provides a soft anti-cold medicine capsule and its preparation process and belongs to the field of medicine technology. The content consists of active medicine component and stuffing, the active medicine component includes acetaminophen, pseudoephedrine hydrochloride and dextromethorphan hydrobromide, and the stuffing includes dispersing medium, surfactant, suspension assistant and microemulsifier. The present invention has fast acting and obvious curative effect on cold syndrome, and the soft capsule is clear and transparent.

Cephalofruxin ester liposome, its preparation and medicinal composition containing it

Acemetacin sustained-release preparation and preparation method

The present invention relates to an acemetacin sustained-release preparation and the preparation method, which pertains to the field of pharmaceutical technology and is used for solving the problems of the short plasma half-life time and short lasting time of the treatment of acemetacin. The present invention is composed of a drug core of acemetacin and controller-release layers wrapping the drug core, the controller-release layer is composed of the xanthan gum-chitosan mixture, wherein, the content of the xanthan gum accounts for 20 percent to 80 percent of the total weight of the xanthan gum-chitosan. The present invention is provided with a plurality of controller-release layers which wrap the outside of the drug core of acemetacin, so as to slow down the release speed of the drug by increasing the number of the layers of the controller-release layers or the wrapping rate. The trials show that the preparation can better control the release of the drug compared with the conventional preparations ...

Freeze dried powder injection of tramadol hydrochloride and its preparation process

Antipyretic and analgetic aspirin enteric-coated preparation and production thereof

An enteric composite aspirin for antipressis and analgesia is proportionally prepared from aspirin, VC, filler, disintegrant, lubricant, moistening agent or adhesive, and enteric coating material.

Cefadroxil dry suspension and preparing method

The present invention relates to dry cefadroxil suspension and its preparation process, belongs to the field of medicine technology, and is for raising the water solubility and bioavailability of cefadroxil. The dry cefadroxil suspension consists of cefadroxil and supplementary material comprising including agent, water soluble stuffing, distintegrating agent, suspension assistant and adhesive. The dry cefadroxil suspension has the features of high medicine solubility, high medicine bioavailability, high chemical stability, good taste, convenient taking, high patient's compliance, full absorption in gastrointestinal tract, less irritation to gastrointestinal tract of medicine, etc.

Method for purifying chicken marination processing byproduct chicken oil

The invention discloses a method for purifying a chicken marination processing byproduct chicken oil. The method comprises the following steps of: (1) degumming, namely mixing a byproduct chicken oil generated in chicken marination processing and solution of phosphoric acid, stirring, and centrifuging to remove lower-layer colloidal impurities, wherein the mass ratio of the phosphoric acid to thechicken oil is (0.1-0.2):100; (2) performing alkali refining, namely adding alkali liquor into the treated chicken oil, slowly stirring, heating for 30min, standing for 15min, removing lower-layer nigre to which impurities are absorbed, washing for 2 to 3 times by using water, and performing centrifugal separation to remove a water layer; and (3) drying and dehydrating, namely drying the chicken oil under vacuum conditions until the content of the moisture is less than 0.3 percent. The chicken marination processing byproduct is taken as a raw material, the cost is low, and the method is convenient ...

Oxiracetam preparation and method of preparing the same

The invention provides an oxiracetam agent and the preparation method, which relates to medical technical field and is used to induce the drug to penetrate through blood-brain barrier and to improve treatment effects. The agent contains oxiracetam nano-particle and excipientpharmaceutical excipient. After improved, the oxiracetam nano-particle and excipientpharmaceutical excipient contains drug core and a modified layer. The drug core mainly comprises principal agent and carrier, wherein the carrier is polymer material containing amino polysaccharide with a content of 70 to 95 percent, and the principal agent is oxiracetam with a content of 5 to 30 percent. The invention adopts polymer material containing amino polysaccharide as carrier to carry the oxiracetam and endow the oxiracetam with good brain targeting function. And the invention adopts surfactant to modify the nano surface of the carrier and lengthens the recycling time of the carrier nano-granule and the nano-particle in the recycling ...

Improved malus asiatica soft capsule and its preparation method

Injecting Mailuoning, its preparation and quality control thereof

Salt roasted chicken product and preparation method thereof

The invention discloses a salt roasted chicken product and a preparation method thereof. The preparation method comprises the following steps of: (1) salting; (2) precooking; (3) marinating; (4) colouring, carrying out oxidation and protecting colour; (5) roasting a chicken in salt; (6) cutting and reshaping, drying and then cooling, and then packaging with inner package, carrying out microwave sterilization on a packaged and unsealed product, then vacuumizing the sterilized packaging product, and carrying out heat sealing on a package opening to obtain a semi-finished product; and (7) sterilizing the semi-finished product at a high temperature and high pressure, cleaning, and carrying out air drying to obtain the salt roasted chicken product. The salt roasted chicken product discloses by the invention not only can show unique colour, lustre, taste and flavour of the traditional salt roasted chicken product but also is greatly improved, the salt content is greatly reduced, the chicken has ...

Novel hydrochloric acid tramadol sustained-release tablet and preparation method

The invention discloses a new type sustained release tablets of tramadol hydrochloride and the preparation method. The sustained release tablets comprise tablet core and membrane clothing sheet. The tablet core contains sustained release capsule of tramadol hydrochloride with its weight being 80-90% of total weight of tablet core, and the sustained release capsule is prepared with tramadol hydrochloride and sustained release material with ratio being 1: 1.2-1.5. The sustained release capsule also contains 10% monoglyceride. The sustained release tablet is characterized by stable effective blood concentration, increased biological utilization rate, reduced side effect, good taste and small intake amount of one time per day.

Agastachel patchoule summer heat dispelling soft capsule and its preparation method

Easy-to-administrate oxiracetam granular formulation and preparation method

The invention relates to an easy-to-take oxiracetam particle preparation and a preparation method, which pertains to the technical field of medicine and is used for solving the problems of stability and inconvenient administration. The preparation comprises oxiracetam nano-particles and pharmaceutical excipients, the mix ratio by weight units of the main drug oxiracetam and the pharmaceutical excipients after the improvement is 1.195: 1, the pharmaceutical excipients are composed of mannitol, asipatan, sunset yellow and powdered fragrances, and the mix ratio by weight units of the ingredientsof the pharmaceutical excipients is 440: 5: 0.2: 1. The selection of the excipients in a formula of the preparation of the invention, the mix ratio of the main drug and the excipients and the mix ratio relationship among the excipients are accurate and reasonable, thus being characterized by easy water solubility, better smell and convenient administration, more particularly, the administration by the ...

Novel hydrochloric acid tramadol sustained-release tablet

The invention discloses a new type sustained release tablets of tramadol hydrochloride and the preparation method. The sustained release tablets comprise tablet core and membrane clothing sheet. The tablet core contains sustained release capsule of tramadol hydrochloride with its weight being 80-90% of total weight of tablet core, and the sustained release capsule is prepared with tramadol hydrochloride and sustained release material with ratio being 1: 1.2-1.5. The sustained release capsule also contains 10% monoglyceride. The sustained release tablet is characterized by stable effective blood concentration, increased biological utilization rate, reduced side effect, good taste and small intake amount of one time per day.

Antipyretic and analgetic aspirin enteric-coated preparation and production thereof

No-sugar Mailuoning granule and its preparing process and quality control method

Preparation method of a novel soft capsule for clearing heat and detoxifying

The invention discloses a new making technique of heat clearing and detoxicating soft-capsule, which is characterized by the following: leaching needed medicine in the acid and alkaline environment through ultrasound; condensing the effective component; blending with dispersing dielectric, suspension-assisting agent and surface activator evenly; packing through soft capsule without freezing and sediment.

CIRCUIT TEACHING DEVICE WITH CARDS AND SOCKET CONNECTING UNITS

Easy-to-administrate oxiracetam granular formulation and preparation method

The invention relates to an easy-to-take oxiracetam particle preparation and a preparation method, which pertains to the technical field of medicine and is used for solving the problems of stability and inconvenient administration. The preparation comprises oxiracetam nano-particles and pharmaceutical excipients, the mix ratio by weight units of the main drug oxiracetam and the pharmaceutical excipients after the improvement is 1.195: 1, the pharmaceutical excipients are composed of mannitol, asipatan, sunset yellow and powdered fragrances, and the mix ratio by weight units of the ingredients of the pharmaceutical excipients is 440: 5: 0.2: 1. The selection of the excipients in a formula of the preparation of the invention, the mix ratio of the main drug and the excipients and the mix ratio relationship among the excipients are accurate and reasonable, thus being characterized by easy water solubility, better smell and convenient administration, more particularly, the administration by ...

Method for biological equivalence detection of alendronate sodium

伤口烧烫伤药粉

A Chinese medicine in the form of powder for treating burn and scald by external application is prepared from 3-6 Chinese-medicinal materials including rhubarb, egg shell, dried chicken droppings, borneol, etc. Its advantages are high healing speed, high curative effect and low cost.

Injectable azithromycin freeze-dried powder, and its preparation method

Alendronate pharmaceutical composition and its preparation technique

Chinese medicinal composition for treating restenosis after coronary intervention and preparation method thereof

The invention provides a traditional Chinese medicine composition for treating restenosis after coronary heart disease interventional therapy and a preparation method thereof. The traditional Chinese medicine composition comprises the root of red-rooted salvia, the root bark of the peony tree, honeysuckle and milk veteh. The traditional Chinese medicine composition is prepared by extracting raw material medicines which are prepared into the preparation. The traditional Chinese medicine composition has the efficacy of cooling blood and regenerating tissue and is mainly used for treating restenosis after coronary heart disease interventional therapy.

Chinese medicinal composition for treating restenosis after coronary intervention and preparation method thereof

The invention provides a traditional Chinese medicine composition for treating restenosis after coronary heart disease interventional therapy and a preparation method thereof. The traditional Chinese medicine composition comprises the root of red-rooted salvia, the root bark of the peony tree, honeysuckle and milk veteh. The traditional Chinese medicine composition is prepared by extracting raw material medicines which are prepared into the preparation. The traditional Chinese medicine composition has the efficacy of cooling blood and regenerating tissue and is mainly used for treating restenosis after coronary heart disease interventional therapy.

Medicine composition for treating osteoporosis or preventing bone fracture caused by osteoporosis and its application

The present invention provides a pharmaceutical composition containing alendronate or the pharmaceutical acceptable salt thereof and parathyroid hormone or the derivatives thereof, the pharmaceutical composition can also be added with vitamin D and calcium salt. The pharmaceutical composition of the present invention can be used for the treatment of osteoporosis, on the one hand, the present invention can inhibit the bone resorption fundamentally, on the other hand, the present invention can increase the bone mass and improve the bone formation, the two-pronged approach can ensure the patients to get the scientific and comprehensive treatment, so as to achieve the purposes of treatment of osteoporosis, the prevention of occurrence of bone fracture and the treatment of the fractures caused by osteoporosis.

Enteric soluble preparation of Alun phosphorate and its preparing method

An enteric allenphosphonate in the form of tablet or capsule is prepared from allenphosphonate, medicinal auxiliary and enteric coating.

Pharmaceutical composition for treating chronic stable angina pectoris with hyperlipemia

The invention relates to a pharmaceutical composition for treating chronic stable angina pectoris with hyperlipermia, which comprises the components of a drug carrier, a sino atrial node If current selective specificity inhibitor or pharmaceutical salt thereof, and an HMG-CoA reductase selective depressant or pharmaceutical salt thereof; the sino atrial node If current selective specificity inhibitor or the pharmaceutical salt thereof is Ivabradine hydrochloride; and the contents of the components of the medical composition by mass unit are 2.5 to 10 of the sino atrial node If current selective specificity inhibitor and 2.5 to 100 of the HMG-CoA reductase selective depressant. The medical composition has good synergistic effect when treating the chronic stable angina pectoris with the hyperlipermia, and has good effect of lowering hyperlipemia for hyperlipoidemia and hemorheology effect.

Acemetacin sustained-release preparation and preparation method