Injectable Acylhydrazone-Linked RAFT Polymer Hydrogels for Sustained Protein Release and Cell Encapsulation.
Injectable Acylhydrazone-Linked RAFT Polymer Hydrogels for Sustained Protein Release and Cell Encapsulation.
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用于持续蛋白质释放和细胞封装的可注射酰腙连接 RAFT 聚合物水凝胶。
DOI:
10.1002/adhm.202101284
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发表时间:
2022-04
影响因子:
10
通讯作者:
Lin CC
中科院分区:
文献类型:
--
作者:
Lin FY;Dimmitt NH;Moraes de Lima Perini M;Li J;Lin CC
A new class of temperature responsive polymer, termed PADO, is synthesized by reversible addition-fragmentation chain-transfer (RAFT) polymerization. Synthesized from copolymerization of diacetone acrylamide (DAAM), di(ethylene glycol) ethyl ether acrylate (DEGA), and oligo(ethylene glycol) methyl ether acrylate (OEGA), PADO polymer phase separates at temperature above its LCST (36°C to 42°C) due to enhanced hydrophobic interactions between the short ethylene glycol side chains. Solution of PADO polymers exhibited injectable shear-thinning properties and reached sol-gel transition rapidly (< 5 min) at 37°C. When the ketone moieties on DAAM were linked by adipic acid dihydrazdie (ADH), PADO polymers formed crosslinked and injectable acylhydrazone hydrogels, which were hydrolytically degradable at a mild acidic environment owing to the pH sensitive acylhydrazone bonds. The pH-responsive degradation kinetics could be controlled by tuning polymer contents and ketone/hydrazide ratio. Importantly, the injectable PADO hydrogels were highly cytocompatible and could be easily formulated for pH-responsive sustained protein delivery. A novel class of PADO polymers containing diacetone acrylamide (DAAM), di(ethylene glycol) ethyl ether acrylate (DEGA), and oligo(ethylene glycol) methyl ether acrylate (OEGA) are polymerized via RAFT polymerization. Via acylhydrazone chemistry, the PADO polymers are crosslinked into pH/thermo-sensitive injectable hydrogel for tunable and sustained protein delivery.
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