Effects of free radical initiators on polyethylene glycol dimethacrylate hydrogel properties and biocompatibility

自愈水凝胶 材料科学 聚合 乙二醇 过硫酸铵 自由基聚合 聚乙二醇 PEG比率 乙二醇二甲基丙烯酸酯 生物相容性 化学工程 组织工程 生物医学工程 高分子化学 复合材料 聚合物 经济 冶金 甲基丙烯酸 工程类 医学 财务
作者
Thomas S. Wilems,Xi Lu,Yuki E. Kurosu,Zara Khan,Hyun Ju Lim,Laura A. Smith Callahan
出处
期刊:Journal of Biomedical Materials Research Part A [Wiley]
卷期号:105 (11): 3059-3068 被引量:41
标识
DOI:10.1002/jbm.a.36160
摘要

Abstract Many studies have utilized Irgacure 2959 photopolymerized poly(ethylene glycol) (PEG) hydrogels for tissue engineering application development. Due to the limited penetration of ultraviolet light through tissue, Irgacure 2959 polymerized hydrogels are not suitable for use in tissues where material injection is desirable, such as the spinal cord. To address this, several free radical initiators (thermal initiator VA044, ammonium persulfate (APS)/TEMED reduction–oxidation reaction, and Fenton chemistry) are evaluated for their effects on the material and mechanical properties of PEG hydrogels compared with Irgacure 2959. To emulate the effects of endogenous thiols on in vivo polymerization, the effects of chain transfer agent (CTA) dithiothreitol on gelation rates, material properties, Young's and shear modulus, are examined. Mouse embryonic stem cells and human induced pluripotent stem cell derived neural stem cells were used to investigate the cytocompatibility of each polymerization. VA044 and Fenton chemistry polymerization of PEG hydrogels both had gelation rates and mechanical properties that were highly susceptible to changes in CTA concentration and showed poor cytocompatibility. APS/TEMED polymerized hydrogels maintained consistent gelation rates and mechanical properties at high CTA concentration and had a similar cytocompatibility as Irgacure 2959 when cells were encapsulated within the PEG hydrogels. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 3059–3068, 2017.
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