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通过逐步后聚合交联离散的有机铂(II)金属环配合物的 CO 刺激响应型、可注射嵌段共聚物水凝胶。

CO Stimuli-Responsive, Injectable Block Copolymer Hydrogels Cross-Linked by Discrete Organoplatinum(II) Metallacycles via Stepwise Post-Assembly Polymerization.

机构信息

Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University , Shanghai 200062, P. R. China.

The State Key Laboratory of Molecular Engineering of Polymers and Department of Macromolecular Science, Fudan University , Shanghai 200433, P. R. China.

出版信息

J Am Chem Soc. 2017 Oct 4;139(39):13811-13820. doi: 10.1021/jacs.7b07303. Epub 2017 Sep 20.

Abstract

Supramolecular polymeric gels cross-linked by well-defined, discrete metal-organic macrocycles (MOMs) or metal-organic cages have become a prevailing topic within the field of supramolecular self-assembly. However, the realization of supramolecular polymeric hydrogels cross-linked by discrete organometallic architectures with good biocompatibility is still a great challenge. Herein, we present the successful preparation of CO stimuli-responsive, injectable block copolymer hydrogels cross-linked by discrete organoplatinum(II) metallacycles. Through the combination of coordination-driven self-assembly and stepwise post-assembly polymerization, star block copolymers (SBCPs) containing well-defined hexagonal metallacycles as cores were successfully prepared, which featured CO stimuli-responsive properties including CO-triggered morphology transition and CO-induced thermoresponsive behavior. Interestingly, the resultant SBCPs were capable of forming supramolecular hydrogels with MOMs as junctions near physiological temperature, which allowed the realization of a reversible gel-to-sol transformation through the removal and addition of CO. More importantly, the resultant supramolecular hydrogels presented good cytocompatibility in vitro. Therefore, this study provides a new strategy for the construction of new "smart" supramolecular hydrogels with promising applications as biological materials.

摘要

由明确的离散金属有机大环(MOM)或金属有机笼交联的超分子聚合凝胶已成为超分子自组装领域的一个热门话题。然而,实现具有良好生物相容性的离散有机金属架构交联的超分子聚合水凝胶仍然是一个巨大的挑战。在此,我们成功制备了 CO 刺激响应的、可注射的嵌段共聚物水凝胶,其由离散的有机铂(II)金属配合物交联。通过配位驱动自组装和逐步后组装聚合的结合,成功制备了含有明确的六方金属配合物作为核的星形嵌段共聚物(SBCP),其具有 CO 刺激响应特性,包括 CO 触发的形态转变和 CO 诱导的热响应行为。有趣的是,所得的 SBCP 能够在接近生理温度的条件下形成以 MOM 为连接点的超分子水凝胶,通过去除和添加 CO 可以实现可逆的凝胶-溶胶转变。更重要的是,所得的超分子水凝胶在体外具有良好的细胞相容性。因此,本研究为构建具有作为生物材料的应用前景的新型“智能”超分子水凝胶提供了一种新策略。

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