PCL (Polycaprolactone)-Tween 80 copolymer as well as preparation method and application thereof
A polymer and reaction technology, applied in medical science, prosthesis, surgery, etc., can solve problems such as insecurity and human health impact, and achieve simple process, no pollution in the preparation process, good biocompatibility and biological The effect of degradability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] Embodiment 1, preparation PCL-Tween80 copolymer
[0036] Accurately weigh 9g (90% of the total monomer mass) of caprolactone monomer and 1g (10% of the total monomer mass) of Tween 80 as raw materials, and take 0.1% of the total monomer mass of the catalyst stannous octoate and add it to the polymerization tube , carry out vacuum degassing and nitrogen replacement process, repeat three times (to ensure the anaerobic condition of the equipment), seal the polymerization tube, and carry out the ring-opening polymerization reaction under heating in an oil bath at 160°C. After 16 hours of polymerization, the product was cooled and dissolved in methylene chloride, and excess methanol was added to precipitate the copolymer. Methanol unreacted monomer and Tween 80 were removed by filtration. The resulting precipitate was vacuum-dried at 45°C for 48 hours to obtain the PCL-Tween80 copolymer provided by the present invention.
[0037] The results of Fourier transform infrared s...
Embodiment 2
[0042] Embodiment 2, preparation PCL-Tween 80 copolymer
[0043] Accurately weigh 6g (monomer total mass 60%) caprolactone monomer and 4g (monomer total mass 40%) Tween 80 as raw materials, take 0.1% catalyst stannous octoate of monomer total mass and add in the polymerization tube , carry out the vacuum degassing and nitrogen replacement process, repeat three times (to ensure the anaerobic condition of the equipment), seal the polymerization tube, and carry out the ring-opening polymerization reaction under heating in an oil bath at 140°C. After 12 hours of polymerization, the product was cooled and dissolved in methylene chloride, and excess methanol was added to precipitate the copolymer. Methanol unreacted monomer and Tween 80 were removed by filtration. Vacuum dry the resulting precipitate at 45°C for 48 hours to obtain a PCL-Tween 80 copolymer with a molecular weight of 1000. In formula I, x is an integer of 2-14, y is an integer of 2-14, and z is an integer of 2-14 , ...
Embodiment 3
[0044] Embodiment 3, preparation PCL-Tween 80 copolymer
[0045] Accurately weigh 9.9g (monomer total mass 99%) caprolactone monomer and 0.1g (monomer total mass 1%) Tween 80 as raw material, get 0.1% catalyst stannous octoate of monomer raw material gross mass and add polymerization In the tube, the process of vacuum degassing and nitrogen replacement was carried out three times (to ensure the anaerobic condition of the equipment), the polymerization tube was sealed, and the ring-opening polymerization reaction was carried out under heating in an oil bath at 160°C. After 16 hours of polymerization, the product was cooled and dissolved in methylene chloride, and excess methanol was added to precipitate the copolymer. Methanol unreacted monomer and Tween 80 were removed by filtration. The resulting precipitate was vacuum-dried at 45°C for 48 hours to obtain a PCL-Tween 80 copolymer with a molecular weight of 43,000. 17, wherein, w+x+y+z=20, l is 2-365, m is 2-365, n is 2-365,...
PUM
| Property | Measurement | Unit |
|---|---|---|
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com
