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A Versatile Monomer for Preparing Well-Defined Functional Polycarbonates and Poly(ester-carbonates).一种用于制备结构明确的功能性聚碳酸酯和聚(酯-碳酸酯)的通用单体。
Macromolecules. 2011 Apr 26;44(8):2660-2667. doi: 10.1021/ma200021m.
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Hyaluronic acid hydrogels for biomedical applications.透明质酸水凝胶在生物医学中的应用。
Adv Mater. 2011 Mar 25;23(12):H41-56. doi: 10.1002/adma.201003963. Epub 2011 Mar 10.
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The performance of human mesenchymal stem cells encapsulated in cell-degradable polymer-peptide hydrogels.细胞可降解聚合物-肽水凝胶包封的人骨髓间充质干细胞的性能。
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Biocompatible copper(I) catalysts for in vivo imaging of glycans.用于聚糖体内成像的生物相容铜(I)催化剂。
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Peptide-Functionalized Click Hydrogels with Independently Tunable Mechanics and Chemical Functionality for 3D Cell Culture.用于3D细胞培养的具有独立可调力学性能和化学功能的肽功能化点击水凝胶
Chem Mater. 2010 Aug 24;22(16):4783-4790. doi: 10.1021/cm101391y. Epub 2010 Jul 22.
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Live-cell imaging of cellular proteins by a strain-promoted azide-alkyne cycloaddition.通过应变促进的叠氮化物-炔烃环加成对细胞蛋白质进行活细胞成像。
Chembiochem. 2010 Oct 18;11(15):2092-5. doi: 10.1002/cbic.201000419.
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Mineralization of hydrogels for bone regeneration.水凝胶的矿化用于骨再生。
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Methods for photocrosslinking alginate hydrogel scaffolds with high cell viability.具有高细胞活力的藻酸盐水凝胶支架的光交联方法。
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Visualizing enveloping layer glycans during zebrafish early embryogenesis.可视化斑马鱼早期胚胎发生过程中的被膜层聚糖。
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无铜应变促进点击化学交联的细胞相容聚(乙二醇)-共聚碳酸酯水凝胶。

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

机构信息

Department of Orthopedics & Physical Rehabilitation, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.

出版信息

Chem Asian J. 2011 Oct 4;6(10):2730-7. doi: 10.1002/asia.201100411. Epub 2011 Aug 24.

DOI:10.1002/asia.201100411
PMID:21954076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3689886/
Abstract

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 "clicking" 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.

摘要

用于再生医学应用的策略是将细胞封装在具有可调机械性能和可降解性的细胞相容性三维水凝胶中,而不会产生有害的凝胶条件。在这里,我们报道了一种通过无铜应变促进叠氮化物-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。通过在生理条件下将叠氮基功能化的聚(乙二醇)-共-聚碳酸酯大分子单体与二苯并环辛炔功能化的聚(乙二醇)点击,在数分钟内形成具有不同机械性能的水凝胶。与包封在光交联聚乙二醇二甲基丙烯酸酯中的细胞相比,包封在这些凝胶中的骨髓基质细胞表现出更高的细胞活力。对大分子单体组成、细胞相容性 SPAAC 交联和聚碳酸酯段的可降解性的精确控制使这些水凝胶成为支架和干细胞辅助组织修复和再生的有前途的候选物。