Yak collagen peptide and application thereof
A collagen peptide and collagen technology, applied in yak collagen peptide and its application field, can solve the problems that imported collagen peptide occupies market share, is not as popular as fish source collagen peptide, and has a low market position, so as to achieve self-improvement Effects of metabolism and repair ability, improvement of SOD activity, and promotion of proliferation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] A yak collagen peptide, the specific steps of its preparation method are as follows:
[0025] (1) Pretreatment: Weigh fresh yak hide, chop it into 1×1cm blocks after depilation, add soda ash with a mass concentration of 5% at room temperature for 8 hours at a material-to-liquid mass ratio of 1:5kg / kg, and soak for 8 hours. After the end, wash the yak skin with water until it is neutral, and then add the yak skin to the mass concentration of 5% salt at a mass ratio of 1:5kg / kg and soak it again for 8 hours. to achieve the purpose of degreasing and removing impurities;
[0026] (2) Homogenization: add 0.05M acetic acid solution into 0.05M acetic acid solution with colloid mill to obtain yak hide homogenate according to the mass ratio of material to liquid after pretreatment;
[0027] (3) Enzymolysis:
[0028] The first enzymatic hydrolysis: Add 1.5g of pepsin with an enzyme activity of 100,000 to the yak hide slurry obtained by homogenizing in step (2), and then heat it...
Embodiment 2
[0039] The effect of yak yak collagen peptide on the proliferation of human fibroblasts was detected by CCK8 method.
[0040] Human fibroblast HFF-1 in DMEM medium (containing 10% fetal bovine serum) in 5% CO 2 , cultured in a carbon dioxide incubator with a constant temperature of 37°C. Take the fibroblasts in the exponential growth phase after subculture, and adjust the cell density to 2.5×10 4 cells / mL, inoculated in 96-well plate, 100 μl per well, cultured in 37°C, 5% CO2 incubator for 24 hours, then added the sample (the sample was dissolved in DMEM culture solution and filtered with a 0.22 μm filter) to make the final concentration Reached 0.312, 3.12, 12.5mg / mL. After continuing to cultivate for 48 hours, aspirate the culture solution and add 100 μl of 10% CCK8, place in a carbon dioxide incubator and culture for 2 hours, use a multi-functional microplate reader to detect the absorbance (OD value) at 450 nm, and finally calculate the cell survival rate of each group. ...
Embodiment 3
[0043] After the yak collagen peptide of the present invention treats the fibroblasts, the intracellular SOD activity is measured.
[0044] After the fibroblasts are treated with the yak collagen peptide of the present invention, a superoxide dismutase (SOD) activity detection kit (Beijing Suolaibao Technology Co., Ltd.) is selected for the determination of intracellular SOD activity.
[0045]Human fibroblast HFF-1 in DMEM medium (containing 10% fetal bovine serum) in 5% CO 2 , cultured in a carbon dioxide incubator with a constant temperature of 37°C. Take the fibroblasts in the exponential growth phase after subculture, and adjust the cell density to 1×10 6 cells / mL, seeded in a six-well plate, 100 μl per well, at 37°C, 5% CO 2 After culturing for 24 hours in an incubator, add samples (the samples were dissolved in DMEM culture solution and filtered with a 0.22 μm filter) so that the final concentrations reached 0.312, 3.12, and 12.5 mg / mL. After 48 h of culture, the dige...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com