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环糊精在药物传递中的应用:探索支架、性质和前沿应用。

Cyclodextrin in drug delivery: Exploring scaffolds, properties, and cutting-edge applications.

机构信息

Department of Mechanical Engineering, University of Connecticut, Connecticut, United States.

Department of Chemistry, Hemvati Nandan Bahuguna Garhwal University (A Central University), Srinagar, Garhwal, Uttarakhand, India.

出版信息

Int J Pharm. 2024 Sep 5;662:124485. doi: 10.1016/j.ijpharm.2024.124485. Epub 2024 Jul 17.

Abstract

Cyclodextrins (CDs) are unique cyclic compounds that can form inclusion complexes via host-guest complexation with a wide range of molecules, thereby altering their physicochemical properties. These molecules offer the formation of inclusion complexes without the formation of covalent bonds, making them suitable for a variety of applications in pharmaceutical and biomedical fields. Due to their supramolecular host-guest properties, CDs are being utilized in the fabrication of biomaterials, metal-organic frameworks, and nano-drug carriers. Additionally, CDs in combination with biomolecules are biocompatible and can deliver nano to macromolecules at the site of drug actions. However, the availability of free hydroxyl groups and a simple crosslinking process for supramolecular fabrication show immense opportunities for researchers in the field of tissue engineering and biomedical applications. In this review article, we have covered the historical development, various types of chemical frameworks, unique chemical and physical properties, and important applications of CDs in drug delivery and biomedical sciences.

摘要

环糊精(CDs)是独特的环状化合物,可通过主客体络合作用与广泛的分子形成包合物,从而改变其物理化学性质。这些分子在不形成共价键的情况下形成包合物,使其适用于药物和生物医学领域的各种应用。由于其超分子主体-客体性质,CD 正在被用于生物材料、金属有机框架和纳米药物载体的制造中。此外,与生物分子结合的 CD 具有生物相容性,并可在药物作用部位递送纳米至大分子。然而,游离羟基基团的可用性和用于超分子制造的简单交联过程为组织工程和生物医学应用领域的研究人员提供了巨大的机会。在这篇综述文章中,我们涵盖了 CDs 在药物传递和生物医学科学中的历史发展、各种化学框架类型、独特的化学和物理性质以及重要应用。

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