Preparation method and product of fibroblasts for skin scar repair
A technology of fibroblasts and fibroblasts, applied in the field of preparation of fibroblasts for skin scar repair and its products, can solve problems such as pigmentation and complications, and inability to remove scars
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] The preparation of embodiment 1 human fibroblast
[0048] The discarded skin was washed three times with 1×PBS (pH 7.4) containing 2 times penicillin and streptomycin, and then 5-20 mL of 0.1% type II collagenase (purchased by Sigma, USA) at a mass volume ratio of 1:1 was used. Digest overnight in a refrigerator at 4°C; after digestion, take dermis tissue with a mass volume ratio of 0.25% trypsin (containing 0.02% EDTA in mass volume ratio) (purchased by Thermo Fisher, USA) and digest it in a 37°C incubator for 4 hours. Then centrifuge at 1500rpm for 10 minutes, discard the supernatant, add normal saline to resuspend, and filter with 100μm cell sieve; cell suspension is centrifuged at 1000rpm for 10 minutes, cell pellet is resuspended and washed twice with normal saline, then add fibroblast serum-free culture medium (Containing 1ng-100ng / ml fibroblast growth factor, purchased by American R&D company; 0.5ng-100ng / ml vitamin E, purchased by American Sigma company; Identi...
Embodiment 2
[0052] The kit product of the fibroblast used for skin scar repair that embodiment 2 prepares
[0053] The kit of fibroblasts for skin scar repair includes:
[0054] 1) 500ml serum-free medium for fibroblasts;
[0055] 2) 10 4 IU / mL type II collagenase;
[0056] 3) 100ml 0.25% trypsin;
[0057] 4) 10mL 50 times active composition: 50ng-5μg fibroblast growth factor, 25ng-5μg vitamin E, 5mg-100mg phosphate-3-O-rutinoside, 5mg-100mg L-lactic acid;
[0058] 5) 10mL 50 times serum-free supplement;
[0059] 6) instruction manual;
[0060] Wherein, the instructions for use include the methods described in Examples 1-3.
Embodiment 3
[0061] Example 3 In vitro co-culture of human fibroblasts inhibits the proliferation of hypertrophic scar fibroblasts
[0062] Hypertrophic scar fibroblasts in the logarithmic growth phase (purchased from ScienCell, USA) were taken in 3 × 10 5 The concentration of cells / well was inoculated in 6-well Transwell culture plates (0.3 μm, Corning Company, USA), cultured in UltraCULTURETM without serum, 1.5 mL was inoculated in each well, and human fibroblasts were added to the small chamber, 3×105 cells / chamber, 1.5 ml, placed at 37 ℃, 5% CO2 incubator co-cultivation, for grouping. Blank control group A: No fibroblast co-culture (Control) was added to the small chamber, 6 repeated wells; fibroblast experiment group B prepared in Example 1: normal fibroblasts (FB) were added to the small chamber for co-culture, repeated wells 6; and the fibroblast control group C of comparison ratio culture (comparison ratio fibroblast adopts " in adding fibroblast growth factor and not adding in th...
PUM
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