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Process for preparing phosphatidylserine salts

A technology of phosphatidylserine salt and phosphatidylserine, which is applied in the field of preparation of phosphatidylserine salt, can solve the problems of increasing, affecting the content of phosphatidylserine, affecting the effect of alcohol removal of impurities, etc., to expand the application range, improve the effect of removing impurities, The effect of increasing the content of phosphatidylserine

Active Publication Date: 2020-08-14
NANTONG LICHENG BIOLOGICAL ENG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The phosphatidylserine prepared by the prior art exists in the form of calcium salt, and phosphatidylserine calcium salt is insoluble in most organic solvents such as oil, alcohol, alkanes, etc., which limits the application of phosphatidylserine, and in the purification process Among them, the calcium salt form of other phospholipids is insoluble in organic solvents such as ethanol, which affects the impurity removal effect of organic solvents such as alcohol, and ultimately affects the increase in the content of phosphatidylserine in the product

Method used

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  • Process for preparing phosphatidylserine salts
  • Process for preparing phosphatidylserine salts
  • Process for preparing phosphatidylserine salts

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0099] Add 200g of L-serine, 16g of calcium chloride and 600ml of purified water in 100g of soybean lecithin with a phosphatidylcholine content of 52%, at a constant temperature of 45°C, after stirring for one hour, add 10ml of phospholipase D solution, React at a constant temperature of 45° C. for four hours to obtain a mixture containing calcium salt of phosphatidylserine.

[0100] The mixture containing calcium salt of phosphatidylserine was centrifuged and the supernatant solid was removed.

[0101] Add 500ml of petroleum ether to the upper solid to completely dissolve the upper solid in petroleum ether, then add 300ml of isopropanol and 300ml of water, extract and vibrate, let stand to separate layers, let go of the lower aqueous phase solution, and obtain the first petroleum ether phase solution.

[0102] Add 300ml of an aqueous solution containing 30g of sodium sulfate to the petroleum ether phase solution, react at a temperature of 45°C for 1 hour, and take out the sec...

Embodiment 2

[0109] Add 200g of L-serine, 16g of calcium chloride and 600ml of purified water in 100g of soybean lecithin with a phosphatidylcholine content of 52%, at a constant temperature of 45°C, after stirring for one hour, add 10ml of phospholipase D solution, React at a constant temperature of 45° C. for four hours to obtain a mixture containing calcium salt of phosphatidylserine.

[0110] The mixture containing calcium salt of phosphatidylserine was centrifuged and the supernatant solid was removed.

[0111] Add 500ml of petroleum ether to the upper solid to completely dissolve the upper solid in petroleum ether, then add 300ml of isopropanol and 300ml of water, extract and vibrate, let stand to separate layers, let go of the lower aqueous phase solution, and obtain the first petroleum ether phase solution.

[0112] Add 300ml of an aqueous solution containing 30g of sodium sulfate to the petroleum ether phase solution, react at a temperature of 45°C for 1 hour, and take out the sec...

Embodiment 3

[0118] Add 200g of L-serine, 16g of calcium chloride and 600ml of purified water in 100g of soybean lecithin with a phosphatidylcholine content of 52%, at a constant temperature of 45°C, after stirring for one hour, add 10ml of phospholipase D solution, React at a constant temperature of 45° C. for four hours to obtain a mixture containing calcium salt of phosphatidylserine.

[0119] The mixture containing calcium salt of phosphatidylserine was centrifuged and the supernatant solid was removed.

[0120] Add 500ml of petroleum ether to the upper solid to completely dissolve the upper solid in petroleum ether, then add 300ml of isopropanol and 300ml of water, extract and vibrate, let stand to separate layers, let go of the lower aqueous phase solution, and obtain the first petroleum ether phase solution.

[0121] Add 300ml of an aqueous solution containing 30g of sodium sulfate to the petroleum ether phase solution, react at a temperature of 45°C for 1 hour, and take out the sec...

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Abstract

The invention discloses a method for preparing a phosphatidylserine salt. The method comprises the following steps of: providing a phosphatidylserine first metal salt; carrying out chemical reaction on solution of the phosphatidylserine first metal salt by solution containing second metal ions so as to obtain a phosphatidylserine second metal salt. By the mode, the method disclosed by the invention has the advantages that not only is the application of the phosphatidylserine expanded, but also the content of the phosphatidylserine in a product is increased.

Description

technical field [0001] The invention relates to the field of food health products, in particular to a method for preparing phosphatidylserine salt. Background technique [0002] Phosphatidylserine is a naturally occurring nutritional phospholipid, which exists in the cell membrane and forms the basic structure of the cell membrane with other phospholipids, and plays an important role in intercellular communication and biochemical information transmission to cells. Especially in the nervous system of the human body, it is one of the important components of the brain cell membrane and plays an important role in regulating various functions of the brain. [0003] The main function of phosphatidylserine is to improve the vitality of brain cells. It has a good effect on the treatment of brain atrophy, prevention of Alzheimer's disease, and improvement of brain function in the elderly; it can repair brain damage and treat ADHD in children; it can also promote the recovery and bala...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07F9/10
CPCC07F9/106
Inventor 夏洪志顾钦青徐晓晓朱宇雷沈宇峰
Owner NANTONG LICHENG BIOLOGICAL ENG