Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation method of high-purity lysophosphatidylcholine

The technology of phosphatidylcholine and phospholipase is applied in the field of preparation of high-purity lysophosphatidylcholine, can solve the problems of many by-products, long reaction time, large amount of monoglyceride added, etc., and achieves stable product properties, The effect of shortening the production cycle and speeding up the response speed

Inactive Publication Date: 2014-12-31
NHWA PHARMA CORPORATION
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Chinese patent CN1210560 expects to improve the hydrolysis effect by adding monoglyceride, but because the reaction temperature is too high and the reaction time is too long, there are still many by-products in the reactant, and the addition of monoglyceride is very large, which is phosphatidylcholine 5 times the amount), the cost is very high
[0004] The phosphatidylcholine hydrolysis method disclosed in the prior art still has some disadvantages, such as low product purity, conversion efficiency of phosphatidylcholine raw material not exceeding 60-70%, glycerol phosphorylcholine and unhydrolyzed phosphatidylcholine When the by-products are high, especially when the phosphatidylcholine with high concentration (concentration is 30-40%) is hydrolyzed, due to the high concentration and the viscosity of the reactant, it takes up to 96 hours of reaction time to convert into lysophosphatidylcholine The efficiency is lower, and the proportion of by-products is higher. In order to obtain high-purity final products, multiple purifications are required to remove by-products, which limits its industrial production.

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
  • Preparation method of high-purity lysophosphatidylcholine
  • Preparation method of high-purity lysophosphatidylcholine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] Add 116ml 0.1mol / L CaCl to the 1000ml reaction bottle equipped with nitrogen protection device 2 Aqueous solution, 50g phosphatidylcholine, 6g sodium cholate, stirred vigorously for 30min to disperse evenly, controlled the initial pH value of the system to 7 by adding 4mol / L NaOH solution, added 1ml phospholipase A2 (Lecitase 10L, 10580IU / ml, Novo Nordisk, Denmark), heated up to 50°C and stirred for 5 hours, cooled to room temperature, slowly added 2L of acetone, precipitated solid, poured out the supernatant, and stirred and washed the solid with 1L of acetone three times, dispersed into powder, suction filtered, 40 ℃ vacuum drying to obtain 25g of powdered lysophosphatidylcholine with a purity of 99.2%.

Embodiment 2

[0021] Add 75ml 0.2mol / L CaCl to the 1000ml reaction bottle equipped with nitrogen protection device 2 Aqueous solution, 50g phosphatidylcholine, 8.22g sodium cholate, stirred vigorously for 30min to disperse evenly, controlled the initial pH value of the system to 8 by adding 4mol / L NaOH solution, added 1ml phospholipase A2 (Lecitase 10L, 10580IU / ml, Novo Nordisk, Denmark), heated up to 50°C and stirred for 5 hours, cooled to room temperature, slowly added 2L of acetone, precipitated solid, poured out the supernatant, and stirred and washed the solid with 1L of acetone three times, dispersed into powder, suction filtered, 40 ℃ vacuum drying to obtain 26.7g powdered lysophosphatidylcholine with a purity of 98.7%.

Embodiment 3

[0023] Add 70ml 0.4mol / L CaCl to the 1000ml reaction bottle equipped with nitrogen protection device 2 Aqueous solution, 50g phosphatidylcholine, 5.48g sodium cholate, stirred vigorously for 30min to disperse evenly, controlled the initial pH value of the system to 7 by adding 4mol / L NaOH solution, added 1ml phospholipase A2 (Lecitase 10L, 10580IU / ml, Novo Nordisk, Denmark), heated to 60°C and stirred for 4 hours, cooled to room temperature, slowly added 2L of acetone, precipitated solid, poured out the supernatant, washed the solid with 1L of acetone for three times, dispersed into powder, and suction filtered, 40 After vacuum drying at ℃, 26 g of powdery lysophosphatidylcholine was obtained with a purity of 99.1%.

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 preparation method of lysophosphatidylcholine. The method comprises the steps: in a calcium ion solution, firstly adding phosphatidylcholine and cholate, stirring, next adding phospholipase A2, carrying out heat preservation, carrying out a hydrolysis reaction to obtain lysophosphatidylcholine, carrying out acetone precipitation, and separating out the product. With addition of the cholate, phosphatidylcholine emulsion droplets become smaller and thinner, the reaction solution becomes diluted, the reactants are completely hydrolyzed in about 5 hours, and the reaction time can be significantly shortened, wherein the phosphatidylcholine concentration reaches up to 30-40%, and the efficiency of converting phosphatidylcholine into lysophosphatidylcholine can still reach 100%. In addition, method by-products such as glycerophosphorylcholine and non-hydrolytic phosphatidylcholine are significantly reduced compared with the prior art. The produced lysophosphatidylcholine has high purity, multi-time purification steps can be omitted, and thus the production cycle can be shortened, and the production cost can be substantially reduced.

Description

technical field [0001] The invention relates to a method for preparing high-purity lysophosphatidylcholine, in particular to a method for preparing high-purity lysophosphatidylcholine from lecithin. Background technique [0002] Lysophosphatidylcholine is a metabolite of lecithin, also known as lysophosphatidylcholine, which can be used as a food additive and emulsifier in the food industry and cosmetics industry. High-purity lysophosphatidylcholine can be used as a drug intermediate in medicine It is a safe and non-toxic drug carrier. For example, in patent CN100536851, as a carrier of valproic acid, its conjugate can be used as a class of excellent antiepileptic drugs, and its preparation usually uses phospholipase A2 to promote the hydrolysis of phosphatidylcholine to produce lysophosphatidylcholine. [0003] It has been known since the beginning of the twentieth century that phosphatidylcholine can be converted to lysophosphatidylcholine by enzymatic hydrolysis. In 193...

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): C12P13/00
Inventor 马彦琴王勇周英珍
Owner NHWA PHARMA CORPORATION