Silk fibroin-gelatin double crosslinked hydrogel and preparation method thereof
A technology of silk fibroin and hydrogel, which is applied in the field of biomedical materials, can solve problems such as complex preparation process and complex mold, and achieve the effect of simple and easy to operate preparation process, strong mechanical properties, and favorable large-scale industrial production
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0050] Preparation of silk fibroin-gelatin double cross-linked hydrogel
[0051] (1) Dissolve 10g of gelatin completely in 5mM 2-morpholineethanesulfonic acid biological buffer at 50°C, add 5g of tyramine hydrochloride after the solution is cooled to room temperature, and then add 1-(3- Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride 0.3675g and N-hydroxysuccinimide 0.1103g, stirred and reacted at room temperature for 12h, after the reaction was completed, the dialysis bag with a molecular weight cut-off of 10000 was dialyzed for 4 days, Freeze-drying at -50°C to obtain tyramide-modified gelatin;
[0052] The H NMR spectra of unmodified gelatin and tyramide-modified gelatin are as follows: figure 1 As shown, the absorption peak of the modified gelatin in the chemical shift range of 6.6~7.1 indicates the hydrogen atom on the phenol group on the tyramide radical, which shows that the modified gelatin has successfully grafted tyramide for enzymatic cross-linking reaction....
Embodiment 2
[0058] Preparation of silk fibroin-gelatin double cross-linked hydrogel
[0059] (1) Dissolve 10g of gelatin completely in 5mM 2-morpholineethanesulfonic acid biological buffer at 50°C, add 5g of tyramine hydrochloride after the solution is cooled to room temperature, and then add 1-(3- Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride 0.3675g and N-hydroxysuccinimide 0.1103g, stirred and reacted at room temperature for 12h, after the reaction was completed, the dialysis bag with a molecular weight cut-off of 10000 was dialyzed for 4 days, Freeze-drying at -50°C to obtain tyramide-modified gelatin;
[0060] See figure 1 As shown, the absorption peak of the modified gelatin in the chemical shift range of 6.6~7.1 indicates the hydrogen atom on the phenol group on the tyramide radical, which shows that the modified gelatin has successfully grafted tyramide for enzymatic cross-linking reaction. root group.
[0061] (2) Soak 4g of degummed silk in 20ml of bromination soluti...
Embodiment 3
[0066] Preparation of silk fibroin-gelatin double cross-linked hydrogel
[0067] (1) Dissolve 10g of gelatin completely in 5mM 2-morpholineethanesulfonic acid biological buffer at 50°C, add 5g of tyramine hydrochloride after the solution is cooled to room temperature, and then add 1-(3- Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride 0.3675g and N-hydroxysuccinimide 0.1103g, stirred and reacted at room temperature for 12h, after the reaction was completed, the dialysis bag with a molecular weight cut-off of 10000 was dialyzed for 4 days, Freeze-drying at -50°C to obtain tyramide-modified gelatin;
[0068] See figure 1 As shown, the absorption peak of the modified gelatin in the chemical shift range of 6.6~7.1 indicates the hydrogen atom on the phenol group on the tyramide radical, which shows that the modified gelatin has successfully grafted tyramide for enzymatic cross-linking reaction. root group.
[0069] (2) Soak 4g of degummed silk in 20ml of bromination soluti...
PUM
Property | Measurement | Unit |
---|---|---|
Strength | aaaaa | aaaaa |
Compressive strength | aaaaa | aaaaa |
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