Preparation method of high-strength light sensitive hydrogel
A high-intensity light and hydrogel technology, applied in the field of high-strength hydrogel preparation, can solve problems such as gel damage and weak hydrogel mechanical properties, and achieve high water absorption, significant photosensitivity, and easy long-term Effects of preservation and long-distance transport
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] Monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (6 mg), SP (0.6 mg) and crosslinker were polymerized Ethylene glycol diacrylate (8.4 mg) was added to a 1.5 ml centrifuge tube, and after dissolving the monomer and cross-linking agent with 210 μl of DMSO, photoinitiator Irgacure 2959 (0.5 mg) was added. The solvent containing monomer, crosslinking agent and initiator was injected into a closed mold, and the mold was irradiated in a UV curing oven for 30 min to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed with deionized water for several times and soaked for 7 days, and the deionized water was replaced every 12 h.
[0033] Cell culture and desorption on the gel surface: The obtained gel was immersed in medical alcohol for 4 hours and then placed in a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. The L929 cell suspension was added to the culture plate wit...
Embodiment 2
[0036] Monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (12 mg), SP (0.9 mg) and crosslinker were polymerized Ethylene glycol diacrylate (12.6 mg) was added to a 1.5 ml centrifuge tube, and after dissolving the monomer and cross-linking agent with 315 μl of DMSO, photoinitiator Irgacure 2959 (0.7 mg) was added. The solvent containing monomer, crosslinking agent and initiator was injected into a closed mold, and the mold was irradiated in a UV curing oven for 30 min to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed with deionized water for several times and soaked for 7 days, and the deionized water was replaced every 12 h.
[0037] Cell culture and detachment on the gel surface: The obtained gel was immersed in medical alcohol for 4 hours and then placed in a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. The L929 cell suspension was added to the culture plate w...
Embodiment 3
[0040] Monomer oligoethylene glycol methacrylate (6 mg), 2-vinyl-4,6-diamino-1,3,5-triazine (18 mg), SP (1.2 mg) and crosslinker were polymerized Ethylene glycol diacrylate (16.8 mg) was added to a 1.5 ml centrifuge tube, and after dissolving the monomer and cross-linking agent with 420 μl of DMSO, photoinitiator Irgacure 2959 (0.9 mg) was added. The solvent containing monomer, crosslinking agent and initiator was injected into a closed mold, and the mold was irradiated in a UV curing oven for 30 min to initiate free radical polymerization. Then the mold was opened to take out the gel, rinsed with deionized water for several times and soaked for 7 days, and the deionized water was replaced every 12 h.
[0041] Cell culture and detachment on the gel surface: The obtained gel was immersed in medical alcohol for 4 hours and then placed in a 96-well plate, and 200 μl of DMEM medium was added to replace the medical alcohol. The L929 cell suspension was added to the culture plate w...
PUM
![No PUM](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/noPUMSmall.5c5f49c7.png)
Abstract
Description
Claims
Application Information
![application no application](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/application.06fe782c.png)
- 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