Skin beautifying and senility resisting preparation and preparation method thereof
A kind of preparation and autologous technology, applied in the field of biomedicine, can solve the problems that the direction and state of proliferation cannot be well controlled, cannot quickly adapt to the internal environment, and the activity of fibroblasts is poor, so as to achieve uniform and rapid repair of wrinkles, Enhanced wrinkle repair effect, orderly and uniform effect of proliferation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] (1) Preparation of autologous fibroblasts
[0037] Pretreatment: Put the collected skin tissue into a petri dish filled with alcohol and soak it for 1 min, wash it with normal saline with 1% double-antibody for 3-5 times, and remove the fat tissue with hemostatic forceps and scissors. Remove cleanly. Double antibody refers to a solution containing penicillin and streptomycin, in which penicillin is 100IU / ml and streptomycin is 100IU / ml.
[0038] Separate the dermis and epidermis: cut the skin tissue into 2×3mm 2 Strips of the same size were digested with 0.25% β-enzyme at 37°C for 1 hour. After digestion is complete, the epidermis is removed and rinsed with normal saline.
[0039] Primary culture: After the dermis is infiltrated with medium containing cytokines, the bottom layer of the dermis (the side where the dermis is in contact with the fat) is spread on the bottom of the T25 culture bottle, and an appropriate interval is left between the dermis to facilitate tiss...
Embodiment 2
[0047] (1) Preparation of autologous fibroblasts
[0048] Pretreatment: Put the collected skin tissue into a petri dish filled with alcohol and soak it for 1 min, wash it with normal saline with 1% double-antibody for 3-5 times, and remove the fat tissue with hemostatic forceps and scissors. Remove cleanly. Double antibody refers to a solution containing penicillin and streptomycin, in which penicillin is 100IU / ml and streptomycin is 100IU / ml.
[0049] Separate the dermis and epidermis: Digest with 4 mg / ml dispase II (Dispase II, neutral protease) at 37°C for 2 hours. After the digestion is complete, remove the epidermis and rinse with normal saline.
[0050] Primary culture: After the dermis is infiltrated with medium containing cytokines, the bottom layer of the dermis (the side where the dermis is in contact with the fat) is spread on the bottom of the T25 culture bottle, and an appropriate interval is left between the dermis to facilitate tissue cells to crawl out. Put t...
Embodiment 3
[0058] This example is basically the same as Example 1, the difference lies in the composition content of the preparation: take 6ml of PRP and 1ml hyaluronic acid for injection and blow the autologous fibroblasts evenly, the content of autologous fibroblasts is 3×10 7 pcs / ml, drawn with a sterile syringe and sealed for use.
[0059] In addition, in the primary culture step, the cytokines and concentrations in the culture medium are respectively: 120ng / ml FGF, 15ng / ml TGF-β and 60ng / ml IGF-I.
PUM
Property | Measurement | Unit |
---|---|---|
quality score | 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