CPC A61F 9/0017 (2013.01) [A61L 27/12 (2013.01); A61L 27/18 (2013.01); A61L 27/20 (2013.01); A61L 27/227 (2013.01); A61L 27/3687 (2013.01); A61L 27/52 (2013.01)] | 7 Claims |
1. A preparation method of a double-network versatile hydrogel with antibacterial and drug sequential release capabilities, comprising the following steps:
(1) mixing 4-(4-hydroxymethyl-2-methoxy-5-nitrophenoxy) butyric acid, tert-butoxycarbonyl-polyethylene glycol-amino and 1H-benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate in a solvent, and adding trifluoroacetic acid for reaction, and then concentrating and precipitating in a pre-cooled diethyl ether to obtain a precipitate;
(2) re-dissolving the precipitate obtained in step (1), mixing with D/L-lactide, glycoluril and stannous isooctoate, concentrating after a reaction, and precipitating in a pre-cooled diethyl ether to obtain a precipitate;
(3) co-blending the precipitate obtained in step (2) with a drug in a solvent and stirring to obtain drug-loaded micelles; and
(4) mixing methacrylate silk fibroin, glycidyl methacrylate functionalized quaternized chitosan, polydeoxyribonucleotide, and lithium phenyl(2,4,6-trimethylbenzoyl) phosphinate with the drug-loaded micelles, followed by cross-linking under irradiation of ultraviolet to construct the double-network versatile hydrogel with antibacterial and drug sequential release capabilities.
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