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Triterpenoid-Based Self-Healing Supramolecular Polymer Hydrogels Formed by Host-Guest Interactions

机译:主体-客体相互作用形成的基于三萜的自修复超分子聚合物水凝胶

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摘要

Pentacyclic triterpenoids, a class of naturally bioactive products having multiple functional groups, unique chiral centers, rigid skeletons, and good biocompatibility, are ideal building blocks for fabricating versatile supramolecular structures. In this research, the natural pentacyclic triterpenoid glycyrrhetinic acid (GA) was used as a guest molecule for -cyclodextrin (-CD) to form a GA/-CD (1:1) inclusion complex. By means of GA and -CD pendant groups in N,N-dimethylacrylamide copolymers, a supramolecular polymer hydrogel can be physically cross-linked by host-guest interactions between GA and -CD moieties. Moreover, self-healing of this hydrogel was observed and confirmed by step-strain rheological measurements, whereby the maximum storage modulus occurred at a [GA]/[-CD] molar ratio of 1:1. Additionally, these polymers displayed outstanding biocompatibility. The introduction of a natural pentacyclic triterpenoid into a hydrogel system not only provides a biocompatible guest-host complementary GA/-CD pair, but also makes this hydrogel an attractive candidate for tissue engineering.
机译:五环三萜类化合物是一类具有多个官能团,独特的手性中心,刚性骨架和良好的生物相容性的天然生物活性产品,是制造通用的超分子结构的理想构建基块。在这项研究中,天然的五环三萜类甘草次酸(GA)被用作-环糊精(-CD)的客体分子,形成GA / -CD(1:1)包合物。借助于N,N-二甲基丙烯酰胺共聚物中的GA和-CD侧基,超分子聚合物水凝胶可以通过GA和-CD部分之间的客体相互作用而物理交联。此外,观察到该水凝胶的自修复并通过分步应变流变学测量证实,由此最大储能模量出现在[GA] / [-CD]摩尔比为1:1时。另外,这些聚合物表现出优异的生物相容性。将天然的五环三萜类化合物引入水凝胶系统,不仅提供了生物相容的客体-宿主互补的GA / CD对,而且使这种水凝胶成为组织工程学的有吸引力的候选人。

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