Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of method of producing nadroparin calcium by heparin sodium crude product

A technology of nadroparin calcium and heparin sodium, which is applied in the production of biochemical raw materials, can solve the problems of difficulty in ensuring the safety of the final product, the quality of heparin sodium, and increasing the pressure on environmental protection, so as to ensure product quality and low energy consumption , The effect of simple preparation process

Active Publication Date: 2017-06-20
NORTH CHINA PHARMA HUAKUN HEBEI BIOTECH
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The heparin sodium removal step in the method is not easy to ensure the quality of heparin sodium used to prepare nadroparin calcium, and barium chloride is also used when preparing nadroparin calcium from heparin sodium, which is highly toxic. If there is residue, the safety of the final product is difficult. Guarantee, and increase environmental pressure

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
  • A kind of method of producing nadroparin calcium by heparin sodium crude product

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Take 1kg of crude heparin sodium, dissolve it in 8L of purified water, add 80g of sodium chloride, raise the temperature to 50°C, and at the same time adjust the pH value to 8.5 with 1mol / L sodium hydroxide solution, and perform salt hydrolysis for 2 hours under this condition. The salt solution was centrifuged to obtain heparin sodium pretreatment solution. Lower the temperature of the heparin sodium pretreatment solution to 28°C, add hydrogen peroxide, the volume of which is 1% of the volume of the heparin sodium pretreatment solution, stir evenly, add to a resin column equipped with 15L OC1074 resin for adsorption, and control the adsorption rate to 0.05 BV / h, the resin after adsorption is first washed with 5.5% sodium chloride solution, the flow rate is 0.5BV / h, and washed to absorbance A 260nm ≤0.20,A 280nmWhen ≤0.20, use 12% sodium chloride solution to elute, the elution rate is 0.05BV / h, detect the refraction of the column liquid, start collecting the eluate whe...

Embodiment 2

[0039] Take 1kg of crude heparin sodium, dissolve it in 10L of purified water, add 200g of sodium chloride, raise the temperature to 60°C, and adjust the pH value to 9.0 with 3mol / L sodium hydroxide solution, and perform salt solution for 3 hours under this condition , and the salt solution was centrifuged to obtain a heparin sodium pretreatment solution. The temperature of the sodium heparin pretreatment solution is down to 32 DEG C, add hydrogen peroxide, its volume is 2% (of the volume of the sodium heparin pretreatment solution, after stirring, add to the resin column that 15L FPA98 resin is housed and carry out adsorption, the control adsorption speed is 0.06BV / h, the resin after adsorption is first washed with 6% sodium chloride solution, the flow rate is 0.5BV / h, and washed to absorbance A 260nm ≤0.20,A 280nm When ≤0.20, elute with 12% sodium chloride solution, the elution rate is 0.06BV / h, detect the refraction of the column liquid, and start collecting the eluate whe...

Embodiment 3

[0041] Take 1kg of crude heparin sodium, dissolve it in 10L of purified water, add 200g of sodium chloride, raise the temperature to 50°C, and at the same time adjust the pH value to 8.5 with 6mol / L sodium hydroxide solution, and perform salt hydrolysis for 2 hours under this condition. The salt solution was centrifuged to obtain heparin sodium pretreatment solution. Lower the temperature of the heparin sodium pretreatment solution to 30°C, add hydrogen peroxide, the volume of which is 1.5% of the volume of the heparin sodium pretreatment solution, stir evenly, add to a resin column equipped with 15L FPA98 resin for adsorption, and control the adsorption rate to 0.05 BV / h, the resin after adsorption is first washed with 5.5% sodium chloride solution, the flow rate is 0.5BV / h, and washed to absorbance A 260nm ≤0.20,A 280nm When ≤0.20, use 12% sodium chloride solution to elute, the elution rate is 0.05BV / h, detect the refraction of the column liquid, start collecting the eluate...

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 discloses a method for producing nadroparin calcium from crude heparin sodium. The method uses crude heparin sodium as raw material, pretreatment by salt solution process, oxidation, ion exchange resin adsorption, washing, elution, and finally ultrafiltration and freeze-drying to obtain heparin sodium fine product, which is then depolymerized , reduction, graded alcohol precipitation, calcium transfer, and freeze-drying to obtain nadroparin calcium. The invention has the advantages of controlling the quality of nadroparin calcium from source and process, short production cycle, low production energy consumption and high product quality, and is suitable for large-scale industrial production.

Description

technical field [0001] The invention belongs to the technical field of production of biochemical raw materials, in particular to a method for producing nadroparin calcium from crude heparin sodium. Background technique [0002] Nadroparin calcium is a low-molecular-weight heparin calcium salt, which is obtained by depolymerizing heparin derived from porcine intestinal mucosa and then grading it with nitrous acid, and selectively removing most sugar chains with a molecular weight less than 2000. It consists of a series of complex oligosaccharides that have not been fully characterized. The non-reducing end is mainly composed of 2-O-thio-α-L-iduronic acid, and the reducing end is mainly composed of 6-O-thio-2,5-anhydro -D-mannitol composition. Its weight average molecular weight should be 3600-5000. Calculated on dry basis, the anti-Xa factor activity is 95IU / mg-130IU / mg, and the ratio of anti-Xa factor potency to anti-IIa factor potency is 2.5-4.0. Nadroparin calcium can b...

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 Patents(China)
IPC IPC(8): C08B37/10
Inventor 段宝玲任风芝张雪霞陈书红高任龙魏松波刘建芬李宁李丽红米文强
Owner NORTH CHINA PHARMA HUAKUN HEBEI BIOTECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products