Polyurethane medical compound film and preparation method thereof
A polyurethane and composite membrane technology, applied in the fields of medical science, bandages, absorbent pads, etc., can solve the problem of lack of biological activity, and achieve the effect of conduction bone growth, convenient use and excellent biocompatibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0032] Take 20 g of polyoxypropylene diol (molecular weight 1000) and 25 g of polycaprolactone diol (molecular weight 1250), stir evenly, heat up to 80°C, and add 4,4'-methylene dicyclohexyl diol dropwise under nitrogen protection. Isocyanate (HMDI) 21.6g, and add 80mg stannous octoate to react for 3.5h to prepare polyurethane prepolymer. Cool down to 40°C, use acetone to prepare the polyurethane prepolymer into a solution with a concentration of 40%, add 3.6ml of 1,4-butanediol, and add N,N-dimethylformamide of nano-hydroxyapatite after half an hour Slurry 86g (the mass fraction of n-HA is 35%), compound under full stirring, add deionized water after 3-4 hours, stir evenly, cast into film, the addition of water is the polyurethane prepolymer content in the solution 1.8%. Then remove the solvent at 55°C, cure at room temperature for 24 hours, then soak in deionized water for 2-4 hours, and carefully peel off to obtain a medical composite film of aliphatic polyurethane with a ...
Embodiment 2
[0034] Get polyoxypropylene trihydric alcohol (molecular weight 1500) 15g, polycarbonate dihydric alcohol (molecular weight 1000) 20g, stir evenly, heat up to 70 ℃, under nitrogen protection, dropwise add isophorone diisocyanate (IPDI) 16g, Add 50 mg of triethylenediamine and react for 4 hours to obtain a polyurethane prepolymer; cool down to 35°C, and use a mixed solvent of ethyl acetate / N,N-dimethylformamide (volume 1:1) to prepolymerize the polyurethane The body is prepared into a solution with a concentration of 45%, adding 3.5ml of diethylene glycol, and adding nano-hydroxyapatite N,N-dimethylformamide slurry 90g after 1 hour (n-HA mass fraction is 40 %), compound under fully stirred state, add deionized water after 3-4 hours, stir evenly, and cast to form a film, the addition of water is 1.5% of the polyurethane prepolymer content in the solution. Then remove the solvent at 50°C, cure at room temperature for 24 hours, soak in deionized water for 2-4 hours, and carefully ...
Embodiment 3
[0036] Polytetrahydrofuran ether (molecular weight: 2000) 30g, castor oil (molecular weight: 932) 6.9g, stir evenly, heat up to 80°C, add lysine diisocyanate (LDI) 10.9g dropwise under nitrogen protection, and add 50mg dibutyltin dilaurate acid ester, and reacted for 3.5h to obtain a polyurethane prepolymer. Cool down to 50°C, use N,N-dimethylacetamide to prepare the polyurethane prepolymer into a solution with a concentration of 30%, add 2.5ml hexanediol, and add nano-hydroxyapatite N,N- 100g of dimethylformamide slurry (the mass fraction of n-HA is 25%), compound under the state of full stirring, add deionized water after 3-4 hours, stir evenly, coat and form a film, the amount of water added is the solution 1% of the polyurethane prepolymer content in the medium. Then remove the solvent at 55°C, cure at room temperature for 24 hours, then soak in deionized water for 2-4 hours, and carefully peel off to obtain a medical composite film of aliphatic polyurethane with a thickn...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
thickness | 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