Synthesis and On-Demand Gelation of Multifunctional Poly(ethylene glycol)-Based Polymers

被引:13
|
作者
Sokolovskaya, Ekaterina [1 ]
Barner, Leonie [1 ,2 ]
Braese, Stefan [2 ,3 ,4 ]
Lahann, Joerg [1 ,2 ,5 ]
机构
[1] KIT, Inst Funct Interfaces IFG, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] KIT, Soft Matter Synth Lab, D-76344 Eggenstein Leopoldshafen, Germany
[3] KIT, IOC, D-76131 Karlsruhe, Germany
[4] KIT, Inst Toxicol & Genet ITG, D-76344 Eggenstein Leopoldshafen, Germany
[5] Univ Michigan, Biointerfaces Inst, Ann Arbor, MI 48109 USA
关键词
aldehydes; crosslinking; hydrogel; photochemistry; poly(ethylene glycol); HYDROGELS; DELIVERY; DOXORUBICIN;
D O I
10.1002/marc.201300909
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The synthesis of a novel photoreactive poly(ethylene glycol) (PEG)-based polymer with caged carbonyl groups is reported. We further demonstrate its use for the on-demand fabrication of hydrogels. For rapid gelation, a hydrazide-functionalized PEG is used as the second component for the hydrogel preparation. The photoreactive PEG-based polymer is designed for controlled cleavage of the protecting groups upon exposure to UV light releases free aldehyde moieties, which readily react with hydrazide groups in situ. This hydrogel system may find applications in controlled release drug delivery applications, when combined with in situ gelation. Furthermore, the possibility of forming gels specifically upon UV irradiation gives an opportunity for 3D fabrication of degradable scaffolds.
引用
收藏
页码:780 / 786
页数:7
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