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Preparation method of fatty acid-based VC lipidosome

A fatty acid-based, fatty acid-based technology is applied in liposome delivery, skin care preparations, medical preparations of non-active ingredients, etc. It can solve the problems of low encapsulation efficiency and damage to the stability of vitamin C, so as to promote absorption, The effect of widening the formation range

Active Publication Date: 2020-08-21
JIANGNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The technical problem to be solved by the present invention is that vitamin C is stable under acidic conditions, while the existing method of utilizing liposomes to embed vitamin C needs to be carried out under neutral or alkaline conditions, which will destroy the stability of vitamin C , and the encapsulation efficiency is low

Method used

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  • Preparation method of fatty acid-based VC lipidosome
  • Preparation method of fatty acid-based VC lipidosome
  • Preparation method of fatty acid-based VC lipidosome

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Embodiment 1 uses the VC liposome prepared by palmitic acid-CLA-SDS

[0049] step one)

[0050] At 60°C, mix 0.1g palmitic acid and 1.3g 95% industrial CLA (CLA average molecular weight 278.73), then add the mixed CLA-palmitic acid to 250mL SDS aqueous solution (the mass concentration of SDS aqueous solution is 0.056%, containing SDS0.14g), simply mixed to obtain a mixture system. The pH of the mixture system was adjusted to pH 3.5 with dilute hydrochloric acid, and a suspension was obtained after homogenization.

[0051] Step (2)

[0052] Add 250mL of 2mg / mL VC aqueous solution dropwise to the above suspension while stirring at 25°C and 150rpm, and the VC aqueous solution will be added dropwise within 30min; shake the mixed solution after adding VC dropwise at 50rpm and 25°C Shake for 30min.

[0053] In the obtained fatty acid-based VC liposome solution, the concentration of fatty acid was 10 mmol / L, and the concentration of VC was 1 mg / mL. The encapsulation effic...

Embodiment 2

[0073] Embodiment 2 uses the VC liposome prepared by palmitic acid-CLA-SDS

[0074] step one)

[0075] At 60°C, 1g of palmitic acid and 13g of 95% industrial CLA (CLA average molecular weight 278.73) were mixed evenly, and then 250mL of SDS aqueous solution (the mass concentration of SDS aqueous solution was 0.56%, containing 1.4g of SDS) was added to the mixed CLA- In palmitic acid, simply mix to obtain a mixture system. Then, adjust the pH of the mixture system to pH 3.5 with dilute hydrochloric acid, and obtain a suspension after homogenization.

[0076] Step (2)

[0077] 250 mL of 10 mg / mL VC aqueous solution was added dropwise to the above suspension while stirring at 25°C and 150 rpm, and the addition was completed within 30 minutes. The mixed solution containing VC was shaken at 30 rpm and 25°C for 90 min.

[0078] In the obtained fatty acid-based VC liposome system, the concentration of fatty acid was 100 mmol / L, the concentration of VC was 5 mg / mL, and the encapsu...

Embodiment 3

[0080] Embodiment 3 uses the VC liposome prepared by stearic acid-CLA-SDS

[0081] step one)

[0082] Mix 1g of stearic acid and 13g of 95% industrial CLA evenly at 60°C, then add 250mL of SDS aqueous solution (the mass concentration of SDS aqueous solution is 0.56%, containing 1.4g of SDS) into the mixed CLA-stearic acid, simply Mix well to obtain a mixture system. Then, the pH of the mixture system was adjusted to pH 3.8 with dilute hydrochloric acid, and a suspension was obtained after homogenization.

[0083] Step (2)

[0084]250 mL of 10 mg / mL VC aqueous solution was added dropwise to the above suspension while stirring at 25°C and 150 rpm, and the addition was completed within 30 minutes. The mixed solution was shaken at 20 rpm for 50 min at 20°C.

[0085] In the obtained fatty acid-based VC liposome system, the concentration of fatty acid is 100mmol / L, the concentration of VC is 5mg / mL, and the encapsulation efficiency of VC is 66.5%.

[0086] Compared with Example...

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Abstract

The invention discloses a preparation method of fatty acid-based VC lipidosome, which belongs to the field of pharmaceutical preparations. According to the invention, a compound of industrial conjugated linoleic acid, other fatty acids and lauryl sodium sulfate is used as a capsule material, and vitamin C is self-assembled and embedded into the capsule material in a water phase under an acidic condition (the pH value is less than 7) to form the fatty acid-based vitamin C liposome. According to the preparation method disclosed by the invention, substances harmful to a human body, such as an organic solvent, are not used, the fatty acid liposome has the characteristics of safety and health, and the prepared fatty acid liposome not only can encapsulate VC under an acidic condition, but also can play a role in slowly releasing VC.

Description

technical field [0001] The invention relates to a preparation method of fatty acid-based VC liposome, belonging to the field of pharmaceutical preparations. Background technique [0002] Vitamin C (Vitamin C, VC), also known as L-ascorbic acid, is a commonly used food additive and the main component of cosmetics, and can be used as an antioxidant in vitamin supplements and cosmetics. However, VC is very unstable in neutral or alkaline aqueous solution. as attached figure 1 Shown: at 25°C, when the initial concentration of VC in deionized water is 0.27mg / mL, VC degrades 29% after 12h; when the temperature is higher than 50°C, after 6h in deionized water, VC The degradation rate can reach 80%. [0003] Therefore, the storage stability of VC is a problem to be solved. In order to enhance the storage stability of VC, the technology of encapsulating VC with various wall materials, such as polysaccharides, proteins, polyethylene or polyethylene glycol, and various liposomes ha...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/127A61K47/12A61K47/20A61K31/375A61P3/02A61K8/67A61K8/36A61K8/14A61Q19/00A23L33/15A23L33/12A23L29/00
CPCA61K9/1271A61K47/12A61K47/20A61K31/375A61P3/02A61K8/676A61K8/361A61K8/14A61Q19/00A23L33/15A23L33/12A23L29/055A23L29/04A23V2002/00A23V2250/708A23V2250/1876A23V2250/188A23V2250/1886A23V2250/1872A61K9/0014A61K8/463A61K9/1278
Inventor 夏咏梅柳欢孟新宇方云樊晔沈洁刘湘
Owner JIANGNAN UNIV