Method for directly producing enoxaparin sodium from crude product heparin sodium

A technology of enoxaparin sodium and heparin sodium, which is applied in the field of preparation of enoxaparin sodium, can solve the problems of high sulfate content in finished products, loose control of starting materials, and large amount of organic solvents used, and achieve stable product quality , Product quality is stable and controllable, and the effect of reducing production costs

Active Publication Date: 2012-07-25
DONGYING TIANDONG PHARM CO LTD
View PDF6 Cites 28 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] In order to solve the above-mentioned technical problems existing in the prior art, the object of the present invention is to provide a method for directly producing enoxaparin sodium from crude heparin sodium, which overcomes the large amount of organic solvent used in the original production process and the control of starting materials. It is not strict, the production process is complicated, and the technical problems of high sulfate content in the finished product

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
  • Method for directly producing enoxaparin sodium from crude product heparin sodium
  • Method for directly producing enoxaparin sodium from crude product heparin sodium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Such as figure 1 As shown, the process described in this embodiment includes the following steps:

[0030] Take 100Kg of crude product heparin sodium, add purified water to dissolve it into a crude product sodium heparin aqueous solution with a concentration of 10wt%; use hydrochloric acid or sodium hydroxide with a concentration of 4mol / L to adjust the pH value of the solution to 5.2, and then add 0.4 times the volume of the solution for medicinal Ethanol, adjust the temperature to 0.5°C, leave it for 6 hours, collect the precipitate a, add purified water 5 times the volume of the precipitate a, after it is completely dissolved, add hydrogen peroxide with a volume of 0.2v% of the solution to oxidize for 6 hours, filter with a filter membrane, Add 2 times the volume of ethanol for precipitation, and place the precipitation for 6 hours to obtain precipitate b; add purified water to dissolve the precipitate b to form a heparin sodium solution with a concentration of 10 wt...

Embodiment 2

[0033] Enoxaparin sodium is realized by the following process. Take 100Kg of crude heparin sodium, add purified water to dissolve it into a crude product heparin sodium aqueous solution with a concentration of 15wt%, use hydrochloric acid or sodium hydroxide with a concentration of 4mol / L to adjust the pH value of the solution to 6.7, Then add medicinal ethanol 0.8 times the volume of the solution, adjust the temperature to 9.5°C, let it stand for 24 hours, collect the precipitate a, add purified water 15 times the volume of the precipitate a, after completely dissolving, add 1v% of the solution volume of hydrogen peroxide to oxidize After 12 hours, filter with a filter membrane, add ethanol in an amount twice the volume of the solution to precipitate, and place the precipitate for 12 hours to obtain precipitate b; add purified water to precipitate b to dissolve it into a heparin sodium solution with a concentration of 15 wt%, and take the precipitate b 4 times the weight of be...

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 relates to a preparation method for directly producing enoxaparin sodium from crude product heparin sodium. The preparation method comprises the following steps of: taking the crude product heparin sodium as a raw material, performing fractionated precipitation through an organic solvent to remove most of impurities in the crude product heparin sodium, and then removing part of residual impurity proteins, pigments and other impurities by oxidation through hydrogen peroxide so as to get the high-purity heparin sodium which is in line with the production requirements of the enoxaparin sodium; and taking the high-purity heparin sodium as an intermediate product, preparing a heparin quaternary ammonium salt, preparing heparin benzyl ester, performing alkaline depolymerization on the heparin benzyl ester, neutralizing with an acid, performing alcohol precipitation, refining, decoloring, dehydrating and drying to get an enoxaparin sodium finished product. By adopting the method disclosed by the invention, the use of the organic solvent is greatly reduced, the production efficiency is improved, the influences on the environment are reduced, the enoxaparin sodium finished product which achieves or is better than European Pharmacopoeia 7.0 version is obtained, and the method is simple to operate and can realize industrialized production.

Description

technical field [0001] The invention relates to a method for preparing enoxaparin sodium, more specifically, the invention relates to a method for directly producing enoxaparin sodium from crude heparin sodium. Background technique [0002] European Pharmacopoeia (EP) Version 7.0 defines enoxaparin sodium (enoxaparinsodium) as a sodium salt of low-molecular-weight heparin, composed of complex oligosaccharides that have not yet been fully characterized, and its structure is characterized by the fact that most components are in the sugar chain. The non-reducing end has a 4-enopyranuronic acid structure, and 15%-25% of the components have a 1,6 anhydride structure at the reducing end. EP7.0 stipulates that the average relative molecular weight of enoxaparin sodium ranges from 3800 to 5000, and the characteristic value is about 4500. The proportion of fractions with molecular weights less than 2000D should be 12.0% to 20.0%, and the proportion of fractions from 2000D to 8000D sh...

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): C08B37/10
Inventor 郭林崔慧斐李荣
Owner DONGYING TIANDONG PHARM CO LTD
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