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刺激响应型环糊精超分子组装体作为药物载体。

Stimuli-responsive cyclodextrin-based supramolecular assemblies as drug carriers.

机构信息

School of Biomedical Engineering, Sun Yat-sen University, Shenzhen, 518107, P. R. China.

Department of Hematology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 518107, P. R. China.

出版信息

J Mater Chem B. 2022 Mar 30;10(13):2077-2096. doi: 10.1039/d1tb02683f.

Abstract

Cyclodextrins (CDs) are widely employed in biomedical applications because of their unique structures. Various biomedical applications can be achieved in a spatiotemporally controlled manner by integrating the host-guest chemistry of CDs with stimuli-responsive functions. In this review, we summarize the recent advances in stimuli-responsive supramolecular assemblies based on the host-guest chemistry of CDs. The stimuli considered in this review include endogenous (pH, redox, and enzymes) and exogenous stimuli (light, temperature, and magnetic field). We mainly discuss the mechanisms of the stimuli-responsive ability and present typical designs of the corresponding supramolecular assemblies for drug delivery and other potential biomedical applications. The limitations and perspectives of CD-based stimuli-responsive supramolecular assemblies are discussed to further promote the translation of laboratory products into clinical applications.

摘要

环糊精(CDs)由于其独特的结构,被广泛应用于生物医学领域。通过将 CD 的主客体化学与刺激响应功能相结合,可以实现各种时空可控的生物医学应用。在本综述中,我们总结了基于 CD 主客体化学的刺激响应超分子组装的最新进展。本综述中考虑的刺激包括内源性(pH、氧化还原和酶)和外源性刺激(光、温度和磁场)。我们主要讨论了刺激响应能力的机制,并介绍了相应超分子组装体用于药物输送和其他潜在生物医学应用的典型设计。讨论了基于 CD 的刺激响应超分子组装体的局限性和展望,以进一步促进实验室产品向临床应用的转化。

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