S-carboxymethyl-L-cysteine complex and enteric preparation composition thereof

A cysteine, enteric-coated preparation technology, applied in the directions of drug combination, pill delivery, drug delivery, etc., can solve the problems of poor stability and only 24 months of validity, reduce gastric irritation symptoms, and improve bioavailability. the effect of reducing irritation

Active Publication Date: 2018-07-27
GUANGZHOU BAIYUNSHAN PHARMA HLDG CO LTD BAIYUNSHAN PHARMA GENERAL FACTORY
View PDF6 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At the same time, the long-term storage stability of the common preparation of S-(carboxymethyl)-L-cysteine ​​is not good, and the validity period is only 24 months

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • S-carboxymethyl-L-cysteine complex and enteric preparation composition thereof
  • S-carboxymethyl-L-cysteine complex and enteric preparation composition thereof
  • S-carboxymethyl-L-cysteine complex and enteric preparation composition thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] S-carboxymethyl-L-cysteine ​​enteric-coated tablet, which contains the following substances in weight ratio:

[0027]

[0028]

[0029] Preparation method:

[0030] Preparation of S-carboxymethyl-L-cysteine ​​clathrate: Take an appropriate amount of S-carboxymethyl-L-cysteine ​​and slowly drop it into the insulated saturated aqueous solution of β-cyclodextrin, stir at a constant temperature and refrigerate. Precipitate was precipitated, filtered, washed and dried.

[0031] Weigh the S-carboxymethyl-L-cysteine ​​clathrate, microcrystalline cellulose, and sodium carboxymethyl starch of the prescribed amount, mix them evenly, pass through an 80-mesh sieve, and prepare them with hypromellose ethanol solution. Granules, 24 mesh granules, the obtained wet granules are dried, add the prescribed amount of talcum powder, mix evenly, 24 mesh granules, and tablet.

[0032] Weigh the enteric-coated layer material of the recipe amount, disperse it with purified water to obta...

Embodiment 2

[0034] S-carboxymethyl-L-cysteine ​​enteric-coated tablet, which contains the following substances in weight ratio:

[0035]

[0036] Preparation method:

[0037] Preparation of S-carboxymethyl-L-cysteine ​​inclusion compound: Dissolve appropriate amount of S-carboxymethyl-L-cysteine ​​in hot water, slowly drop into β-cyclodextrin saturated aqueous solution, 60-80°C Stir vigorously, cool to room temperature, stir at room temperature, refrigerate overnight, precipitate precipitate, filter, wash, and dry.

[0038] Weigh the prescription amount of S-carboxymethyl-L-cysteine ​​inclusion compound, lactose and mannitol mixture, sodium carboxymethyl starch, mix well, pass through 80 mesh sieve, and prepare with hydroxypropyl cellulose ethanol solution Granules, 24 mesh granules, the obtained wet granules are dried, add the prescribed amount of talcum powder, mix evenly, 24 mesh granules, and tablet.

[0039] Weigh the enteric-coated layer material of the recipe amount, disperse ...

Embodiment 3

[0041] S-carboxymethyl-L-cysteine ​​enteric-coated tablet, which contains the following substances in weight ratio:

[0042]

[0043] Preparation method:

[0044] Preparation of S-carboxymethyl-L-cysteine ​​inclusion compound: put an appropriate amount of β-cyclodextrin in a mortar, add 2 times the amount of water to grind, add an appropriate amount of S-carboxymethyl-L-cysteine Amino acid is ground into a paste and obtained after drying.

[0045] Weigh the S-carboxymethyl-L-cysteine ​​inclusion compound of the recipe, microcrystalline cellulose, lactose, mannitol mixture, sodium carboxymethyl starch, after mixing evenly, pass through an 80-mesh sieve, and use hydroxypropyl The methyl cellulose ethanol solution is granulated, granulated at 24 mesh, the obtained wet granules are dried, and the prescription amount of talcum powder is added, mixed evenly, granulated at 24 mesh, and compressed into tablets.

[0046]Weigh the enteric-coated layer material of the recipe amount,...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention provides an S-carboxymethyl-L-cysteine complex with the advantages that the dispersion effect is good; the stimulus of the S-carboxymethyl-L-cysteine on the digestive tract can be effectively reduced; the stability of the medicine and the medicine preparation is enhanced. The enteric preparation containing the complex can avoid the damage in the acid environment in the stomach; the stimulus on the stomach is reduced; the S-carboxymethyl-L-cysteine complex directly reaches the absorption position of the small intestine and is fast dissolved to release active ingredients; the bioavailability of the S-carboxymethyl-L-cysteine complex is improved.

Description

technical field [0001] The invention belongs to the field of pharmaceutical preparations, in particular, the invention relates to an inclusion compound and an enteric-coated preparation thereof. Background technique [0002] S-(carboxymethyl)-L-cysteine, also known as carboxycisteine, was first developed and used clinically by the French Joullie company in 1961. It is a mucolytic drug that can affect the secretion of bronchial glands. Increase the secretion of low-viscosity salivary mucin, reduce the production of high-viscosity fucoidal mucin, and directly act on the disulfide bond of mucin to crack mucin molecules to reduce the viscosity of sputum and make it easier to spit out ; Can improve mucociliary clearance; reduce airway hyperresponsiveness. After CMC enters the body, it is easy to remove the carboxymethyl group to form cysteine, and the sulfhydryl group contained in it can interact with electrophilic groups such as reactive oxygen species (ROS) to exert a direct a...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): A61K47/69A61K31/198A61K9/30A61K9/48A61K9/16A61K47/12A61K47/34A61K47/10A61K47/14A61P11/10A61P11/00A61P11/06
CPCA61K9/1617A61K9/1641A61K9/282A61K9/2853A61K9/4858A61K9/4866A61K31/198
Inventor 王健松王玮肖颖裴泽建朱少璇
Owner GUANGZHOU BAIYUNSHAN PHARMA HLDG CO LTD BAIYUNSHAN PHARMA GENERAL FACTORY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap