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PDMSstar-PEG Hydrogels Prepared via Solvent-Induced Phase Separation (SIPS) and Their Potential Utility as Tissue Engineering Scaffolds

机译:PDMSSTAR-PEG水凝胶通过溶剂诱导的相分离(啜饮)和它们作为组织工程支架的潜在效用制备

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摘要

Inorganic-organic hydrogels based on methacrylated star polydimethylsiloxane (PDMSstar-MA) and diacrylated poly(ethylene glycol) (PEG-DA) macromers were prepared via solvent-induced phase separation (SIPS). The macromers were combined in a dichloromethane (DCM) precursor solution and sequentially photopolymerized, dried and hydrated. The chemical and physical properties of the hydrogels were further tailored by varying the number average molecular weight (Mn) of PEG-DA (Mn = 3.4k and 6k g/mol) as well as the weight % (wt%) ratio of PDMSstar-MA (Mn = 7k g/mol) to PEG-DA from 0:100 to 20:80. Compared to analogous hydrogels fabricated from aqueous precursor solutions, SIPS produced hydrogels with a macroporous morphology, a more even distribution of PDMSstar-MA, increased modulus and enhanced degradation rates. The morphology, swelling ratio, mechanical properties, bioactivity, non-specific protein adhesion, controlled introduction of cell-adhesion, and cytocompatibility of the hydrogels were characterized. As a result of their tunable properties, this library of hydrogels is useful to study material-guided cell behavior and ultimate tissue regeneration.
机译:通过溶剂诱导相分离(SIPS)制备了基于甲基丙烯酸酯化的星形聚二甲基硅氧烷(PDMSstar-MA)和二丙烯酸化的聚乙二醇(PEG-DA)大分子单体的无机-有机水凝胶。将大分子单体在二氯甲烷(DCM)前体溶液中合并,并依次光聚合,干燥和水合。通过改变PEG-DA的数均分子量(Mn)(Mn = 3.4k和6k g / mol)以及PDMSstar-wt的重量%(wt%)比,进一步调整水凝胶的化学和物理性质。 MA(Mn = 7k g / mol)从PEG-DA从0:100到20:80。与由前体水溶液制备的类似水凝胶相比,SIPS生产的水凝胶具有大孔形态,PDMSstar-MA分布更均匀,模量增加和降解速率提高。表征了水凝胶的形态,溶胀率,机械性能,生物活性,非特异性蛋白粘附,细胞粘附的受控引入和细胞相容性。由于其可调性,该水凝胶库可用于研究材料指导的细胞行为和最终的组织再生。

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