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Cytocompatible poly(ethylene glycol)-co-polycarbonate hydrogels cross-linked by copper-free, strain-promoted click chemistry

机译:细胞相容的聚(乙二醇) - 共聚碳酸酯水凝胶通过无铜,应变促进的点击化学交联

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摘要

Strategies to encapsulate cells in cytocompatible three-dimensional hydrogels with tunable mechanical properties and degradability without harmful gelling conditions are highly desired for regenerative medicine applications. Here we reported a method for preparing poly(ethylene glycol)-co-polycarbonate hydrogels through copper-free, strain-promoted azide-alkyne cycloaddition (SPAAC) click chemistry. Hydrogels with varying mechanical properties were formed by \u22clicking\u22 azido-functionalized poly(ethylene glycol)-co-polycarbonate macromers with dibenzocyclooctyne-functionalized poly(ethylene glycol) under physiological conditions within minutes. Bone marrow stromal cells encapsulated in these gels exhibited higher cellular viability than those encapsulated in photo-cross-linked poly(ethylene glycol) dimethacrylate. The precise control over the macromer compositions, cytocompatible SPAAC cross-linking, and the degradability of the polycarbonate segments make these hydrogels promising candidates for scaffold and stem cell assisted tissue repair and regeneration.
机译:对于再生医学应用,非常需要将细胞封装在具有可调节的机械性能和可降解性而没有有害胶凝条件的细胞相容性三维水凝胶中的策略。在这里,我们报道了一种通过无铜,应变促进的叠氮化物-炔烃环加成(SPAAC)点击化学制备聚(乙二醇)-共聚碳酸酯水凝胶的方法。通过在数分钟内在生理条件下用叠氮基官能化的聚(乙二醇)-共聚碳酸酯大分子单体与二苯并环辛炔官能化的聚(乙二醇)单击形成具有不同机械性能的水凝胶。封装在这些凝胶中的骨髓基质细胞比封装在光交联的聚乙二醇二甲基丙烯酸酯中的细胞具有更高的细胞活力。对大分子单体组成的精确控制,细胞相容性SPAAC交联以及聚碳酸酯链段的降解性,使这些水凝胶有望成为支架和干细胞辅助组织修复和再生的候选药物。

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