Acellular dermal matrix guided tissue regeneration membrane material as well as preparation method and application thereof
A technology that guides tissue regeneration and decellularized dermis, applied in tissue regeneration, medical science, prostheses, etc., to achieve the effect of increasing production volume, increasing migration speed, and convenient operation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0032] A preparation method of the acellular dermal matrix-guided tissue regeneration membrane material of the present invention comprises the following steps:
[0033] 1) Pre-treatment: take fish skin, remove fish scales, inner fat and excess fish meat;
[0034] 2) Washing: The fish skin obtained in step 1) is repeatedly rinsed several times with physiological saline, and then, repeatedly rinsed several times with ultrapure water;
[0035] 3) Remove the epidermis and prepare loose noodles: place the tissue obtained in step 1) in a 0.01-1.0mol / L acid solution, shake at 20-37°C for 5-30 minutes, to remove the epidermis and obtain loose noodles ;
[0036] 4) Stabilization: place the tissue obtained in step 3) in a 0.5-2.5 mol / L sodium chloride solution, and shake for 30-120 min at 20-37°C to stabilize the structure;
[0037] 5) Decellularization: freeze-thaw the tissue obtained in step 4) at -80 to -70°C, freeze and thaw several times, and then use 0.5 to 4.0% sodium deoxychol...
Embodiment 1
[0050] A preparation method of the acellular dermal matrix-guided tissue regeneration membrane material of the present invention comprises the following steps:
[0051] 1) Pre-treatment: remove the fish skin from the fish, and remove the fish scales, inner fat and excess fish meat with a knife;
[0052] 2) Washing: The fish skin obtained in step 1) was repeatedly washed with physiological saline for 3 times, each time lasting 10 minutes, and then repeatedly washed with ultrapure water for 3 times, each time lasting 10 minutes;
[0053] 3) Remove the epidermis and prepare loose noodles: put the material obtained in step 2) into 0.01mol / L formic acid solution, and shake for 30 minutes in a constant temperature shaker at 20°C to remove the epidermis and prepare loose noodles;
[0054] 4) Stabilization: put the material obtained in step 3) into a 0.5mol / L sodium chloride solution, and shake for 120 minutes in a constant temperature shaker at 20°C to stabilize the structure;
[00...
Embodiment 2
[0061] A preparation method of the acellular dermal matrix-guided tissue regeneration membrane material of the present invention comprises the following steps:
[0062] 1) Pre-treatment: remove the fish skin from the fish, and remove the fish scales, inner fat and excess fish meat with tweezers;
[0063] 2) Washing: the fish skin obtained in step 1) was repeatedly washed with physiological saline for 5 times, each time lasting 15 minutes, and then repeatedly washed with ultrapure water for 5 times, each time lasting 15 minutes;
[0064] 3) Remove the epidermis and prepare loose noodles: put the material obtained in step 2) into 0.1mol / L hydrochloric acid solution, shake for 10 minutes in a constant temperature shaker at 25°C, remove the epidermis and prepare loose noodles;
[0065] 4) Stabilization: put the material obtained in step 3) into a 1.0mol / L sodium chloride solution, and shake for 90 minutes in a constant temperature shaker at 37°C to stabilize the structure;
[006...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
tensile strength | 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