Preparation method and application of hyperbranched polyester based polyurethane medical adhesive
A technology of hyperbranched polyester and polyurethane, which can be used in applications, surgical adhesives, medical science, etc. It can solve the problems of general adhesion, easy infection, and difficulty in completely covering the bacterial invasion and infection of the wound surface, and the modulus can be adjusted. Large range, good biocompatibility, and comfortable and convenient implementation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0019] The first step is to pass N 2 , Under stirring, add 10gH101 (20mmol, 120mmol of -OH) into a round bottom flask, then slowly drop 3.17ml (40mmol) of acryloyl chloride and an equimolar amount of triethylamine into it, react for more than 24h, and separate and purify it. Precursor 1. The second step is to pass N 2 , Add 4.52gLDI (20mmol) into a round bottom flask under stirring environment, then slowly drop 2gPEG200 (10mmol) into it, and react at 60℃ for >12h to obtain precursor 2. The third step is to pass N 2 , Add 6.52g (10mmol, 20mmol of -NCO) precursor 2 into a round bottom flask under stirring, and then slowly drop 1.52g (2.5mmol, 10mmol of -OH) precursor 1 into it to obtain a Double bond hyperbranched polyester-based polyurethane medical adhesive. In the fourth step, the medical adhesive obtained in the third step is uniformly mixed with the 0.1 wt% photoinitiator i2595, and stored in the dark for use. When in use, apply the medical adhesive to the damaged tissue, ...
Embodiment 2
[0021] The first step is to pass N 2 , Add 12gH201 (20mmol, 120mmol of -OH) into a round bottom flask under stirring environment, then slowly drop 6.34ml (80mmol) of acryloyl chloride and an equimolar amount of triethylamine into it, react for more than 24h, and separate and purify it. Precursor 1. The second step is to pass N 2 , Add 4.52gLDI (20mmol) into a round bottom flask under stirring environment, then slowly drop 2gPEG200 (10mmol) into it, and react at 60℃ for >12h to obtain precursor 2. The third step is to pass N 2 , Add 3.586g (5.5mmol, 11mmol of -NCO) precursor 2 into a round bottom flask under stirring, and then slowly drop 1.52g (2.5mmol, 10mmol of -OH) precursor 1 into it to obtain a Hyperbranched polyester-based polyurethane medical adhesive containing double bonds. In the fourth step, the medical adhesive obtained in the third step is uniformly mixed with 0.5 wt% photoinitiator i2595, and stored in the dark for use. When in use, apply the medical adhesive to...
Embodiment 3
[0023] The first step is to pass N 2 , Add 18.4g of H301 (20mmol, 120mmol of -OH) into a round bottom flask under agitation, then slowly add 4.755ml (60mmol) of acryloyl chloride and an equimolar amount of triethylamine to it, react for more than 24h, separate and purify Get the precursor 1. The second step is to pass N 2 , Add 4.52gLDI (20mmol) into a round bottom flask under stirring environment, then slowly drop 2gPEG200 (10mmol) into it, and react at 60℃ for >12h to obtain precursor 2. The third step is to pass N 2 , Add 4.89g (7.5mmol, 15mmol of -NCO) precursor 2 into a round bottom flask under stirring, and then slowly drop 1.52g (2.5mmol, 10mmol of -OH) precursor 1 into it to obtain a Hyperbranched polyester-based polyurethane medical adhesive containing double bonds. In the fourth step, the medical adhesive obtained in the third step is uniformly mixed with the 0.2wt% photoinitiator i2595, and stored in the dark for use. When in use, apply the medical adhesive to the ...
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