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Deer collagen peptide lipidosome having blood glucose reducing function, and preparation and application thereof

A liposome and blood sugar-lowering technology, which is applied in the direction of liposome delivery, medical preparations containing active ingredients, peptide/protein components, etc., can solve the problem of losing biological activity, etc., and achieve simple methods, easy large-scale production, The effect of expanding the range of application

Inactive Publication Date: 2017-04-05
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Deer collagen peptides have dipeptidyl peptidase inhibitory activity and are used in medicines, health products, food and other fields to play a role in lowering blood sugar. However, as with other active peptides, when bioactive peptides enter the human digestive system orally , Oral deer collagen peptides are easily degraded by proteases in the digestive system, thus losing biological activity

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Prepare deer collagen peptide liposomes according to the following process:

[0022] Using fresh sika deer skin as the raw material, the deer skin is boiled at 50℃ for 30 minutes with a mass concentration of 10% NaOH for degreasing treatment and then cleaned with pure water, cut into pieces of 2 to 3 square centimeters, and the deer skin pieces are in accordance with 1:80 ( Material: buffer mass ratio) was added 0.01M acetate buffer, then pepsin was added at a mass ratio of 1:10 (enzyme: raw material), and the reaction was stirred at 40°C for 1 hour. Adjust the pH of the above reaction solution to 7 with 1M NaOH, add complex enzymes (trypsin, alkaline protease, mass mixing ratio 1:1) for enzymatic hydrolysis, the amount of enzyme added is 0.1% of the mass of the reactant raw materials, at 20°C The reaction was stirred for 1 hour, and the reaction was inactivated at 90°C for 20 minutes. Centrifuge the above reaction solution at 5000 rpm for 5 min, collect the supernatant, ...

Embodiment 2

[0025] Using fresh sika deer tendon as raw material, the deer tendon is boiled in 5% NaOH at 80°C for 10 minutes for degreasing treatment and then cleaned with pure water, cut into pieces of 2 to 3 square centimeters. The deer tendon pieces are according to 1:100 (raw material : Buffer mass ratio) add 0.01M phosphate buffer, then add trypsin at a mass ratio of 1:500 (enzyme: raw material), and react with stirring at 35°C for 10 hours. Adjust the pH of the above reaction solution to 6 with 0.1M HCI, add complex enzymes (papain, bromelain, mass ratio 1:1) for enzymatic hydrolysis, the amount of enzyme added is 1% of the reactant mass, and the reaction is stirred at 50°C After 10 hours, the reaction was inactivated at 100°C for 5 minutes. Centrifuge the above reaction solution at 2000 rpm for 10 min, collect the supernatant, and freeze-dry to obtain deer collagen peptide.

[0026] Take 50 mg of a mixture of dry phospholipids and cholesterol, the mass ratio of phospholipids to chole...

Embodiment 3

[0028] Using fresh red deer tendon as raw material, deer tendon is boiled with 30% NaOH by mass concentration at 70°C for 10 minutes for degreasing treatment and then cleaned with pure water. After ethanol degreasing treatment, it is cleaned with pure water and cut into pieces of 2 to 3 square centimeters. The deer tendon fragments were added with 0.01M phosphate buffer at a mass ratio of 1:10 (raw material: buffer), and then neutral protease was added at a weight ratio of 1:50 (enzyme: raw material), and the reaction was stirred at 45°C for 5 hours. Adjust the pH of the above reaction solution to 8 with 0.5M NaOH, add complex enzymes (papain, alkaline protease, flavor protease, mass ratio 1:1:1) for enzymatic hydrolysis, the amount of enzyme added is 0.5% of the mass of the reactant , Stir the reaction at 60°C for 5 hours, and inactivate at 70°C for 20 minutes after the reaction. Centrifuge the above reaction solution at 8000 rpm for 5 min, collect the supernatant, and freeze-...

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Abstract

The invention relates to a deer collagen peptide lipidosome, and in particularly, provides a deer collagen peptide lipidosome having a blood glucose reducing function, and preparation and application thereof. In the invention, deer collagen peptide is processed into a lipidosome, which has the blood glucose reducing function with inhibition on activity of dipeptidyl peptidase as a target. According to the deer collagen peptide lipidosome, degradation on the deer collagen peptide due to digestive tract enzyme is avoided, so that the deer collagen peptide lipidosome can directly arrive at a target organ to achieve the inhibition on activity of the dipeptidyl peptidase, thereby reducing blood glucose. The product solves a difficult problem that the deer collagen peptide is liable to be degraded by the digestive tract enzyme and is deactivated when being orally taken. The product increases bioavailability of the deer collagen peptide, enlarges dosages of the deer collagen peptide, can be applied in the field of medicine, functional foods, food additives and the like, and has wide application prospect.

Description

Technical field [0001] The invention relates to a deer collagen peptide, in particular to a deer collagen peptide liposome with the function of lowering blood sugar and its preparation and application. Background technique [0002] Dipeptidyl peptidase IV (dipeptidyl peptidase-IV DPP-IV) (EC3.4.14.5) is a serine protease widely distributed in the human body. DPP-IV inactivates the polypeptide by shearing it, so as to regulate physiological functions. DPP-IV preferentially hydrolyzes proteins with proline (Pro) or alanine (Ala) at the second position of the N-terminal. Its substrates include: glucagon-like peptide-1 (GLP217-36), gastric inhibitory peptide (GIP1-42), neuropeptide (NPY), YY peptide (PYY) and pancreatic polypeptide family (PP-family), etc. . The common feature of these substances is that the second amino acid residue at the N-terminal is either proline or alanine residue. DPP-IV plays an important role in diabetes, glucose tolerance, obesity, appetite regulation,...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K38/39A61K9/127A23L33/18A23L29/00A61P3/10
Inventor 邹汉法靳艳
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI