Polypeptide anti-aging composition adopting inclusion technology and preparation method thereof
An inclusion, anti-aging technology, applied in skin care preparations, medical preparations containing active ingredients, pharmaceutical formulas, etc., can solve the problems of harsh storage conditions, easy inactivation of peptides and EGF, etc.
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Embodiment 1
[0029] The polypeptide anti-aging composition of inclusion technology, the content of carnosine is 12-14 parts, the content of acetylglucosamine is 9-11 parts, the content of glutathione is 6-8 parts, and the content of oligopeptide-1 is 7 to 9 parts, and the content of N-hydroxysuccinimide is 7 to 9 parts. Acetyl glucosamine and N-hydroxysuccinimide are located in the hollow sphere, carnosine, oligopeptide-1 and glutathione are adsorbed on the circumference of the hollow sphere, and covered with acetyl glucosamine and N-hydroxysuccinimide .
[0030] The present invention provides another technical solution, a polypeptide anti-aging composition of inclusion technology, comprising the following steps;
[0031] Step 1: Extract and isolate carnosine from muscle tissue, such as anserine β-alanyl-1-methyl L-histidine, cetyl carnosine β-alanyl-3-methyl L-histidine, N- Acetyl-carnosine and other dipeptides are stored in a physiological pH buffer solution with a pH value of 7.0;
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Embodiment 2
[0037] The polypeptide anti-aging composition of inclusion technology, the content of carnosine is 13 parts, the content of acetylglucosamine is 10 parts, the content of glutathione is 7 parts, the content of oligopeptide-1 is 8 parts, N-hydroxy The content of succinimide is 8 parts. Acetyl glucosamine and N-hydroxysuccinimide are located in the hollow sphere, and carnosine, oligopeptide-1 and glutathione are adsorbed on the circumference of the hollow sphere and coated with acetyl glucosamine and N-hydroxysuccinimide
[0038] The present invention provides another technical solution, a polypeptide anti-aging composition of inclusion technology and a preparation method thereof, comprising the following steps;
[0039] Step 1: Extract and isolate carnosine from muscle tissue, such as anserine β-alanyl-1-methyl L-histidine, cetyl carnosine β-alanyl-3-methyl L-histidine, N- Acetyl-carnosine and other dipeptides are stored in a physiological pH buffer solution with a pH value of ...
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