Rapidly in situ forming biodegradable robust hydrogels by combining stereocomplexation and photopolymerization

被引:126
作者
Hiemstra, Christine
Zhou, Wei
Zhong, Zhiyuan
Wouters, Marielle
Feijen, Jan
机构
[1] Univ Twente, Inst Biomed Technol, Fac Sci & Technol, Dept Polymer Chem & Biomat, NL-7500 AE Enschede, Netherlands
[2] TNO Sci & Ind, NL-5600 HE Eindhoven, Netherlands
关键词
D O I
10.1021/ja072113p
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Our previous studies have shown that stereocomplexed hydrogels can be rapidly formed in vitro as well as in vivo upon mixing aqueous solutions of eight-arm poly( ethylene glycol)-poly(L-lactide) (PEGPLLA) and poly( ethylene glycol)-poly( D-lactide) (PEG-PDLA) star block copolymers. In this study, stereocomplexation and photopolymerization are combined to yield rapidly in situ forming robust hydrogels. Two types of methacrylate-functionalized PEG-PLLA and PEG-PDLA star block copolymers, PEG-PLLAMA and PEG-PDLA-MA, which have methacrylate groups at the PLA chain ends and PEG-MA/PLLA and PEG-MA/PDLA, which have methacrylate groups at the PEG chain ends, were designed and prepared. Results showed that stereocomplexed hydrogels could be rapidly formed ( within 1-2 min) in a polymer concentration range of 12.5-17.5% (w/v), in which the methacrylate group hardly interfered with the stereocomplexation. When subsequently photopolymerized, these hydrogels showed largely increased storage moduli as compared to the corresponding hydrogels that were cross-linked by stereocomplexation or photopolymerization only. Interestingly, the storage modulus of stereocomplexed-photopolymerized PEG-PLA-MA hydrogels increased linearly with increasing stereocomplexation equilibration time prior to photopolymerization ( from ca. 6 to 32 kPa), indicating that stereocomplexation aids in photopolymerization. Importantly, photopolymerization of stereocomplexed hydrogels could take place at very low initiator concentrations (0.003 wt %). Swelling/degradation studies showed that combining stereocomplexation and photopolymerization yielded hydrogels with prolonged degradation times as compared to corresponding hydrogels cross-linked by photopolymerization only ( 3 vs 1.5 weeks). Stereocomplexed-photopolymerized PEG-MA/PLA hydrogels degraded much slower than corresponding PEG-PLA-MA hydrogels, with degradation times ranging from 7 to more than 16 weeks. Therefore, combining stereocomplexation and photopolymerization is a novel approach to obtain rapidly in situ forming robust hydrogels.
引用
收藏
页码:9918 / 9926
页数:9
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