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载二维肽纳米片-药物偶联物的注射型壳聚糖水凝胶用于谷胱甘肽响应的持续药物递送。

Injectable Chitosan Hydrogels Doped with 2D Peptide Nanosheet-Drug Conjugates for Glutathione-Responsive Sustained Drug Delivery.

机构信息

College of Chemistry and Chemical Engineering, Qingdao University, 266071, Qingdao, PR China.

Department of Orthopedic Surgery, The Affiliated Hospital of Qingdao University, Qingdao, 266035, PR China.

出版信息

Chemistry. 2024 May 17;30(28):e202400021. doi: 10.1002/chem.202400021. Epub 2024 Apr 10.

Abstract

The development of novel and effective drug delivery systems aimed at enhancing therapeutic profile and efficacy of therapeutic agents is a critical challenge in modern medicine. This study presents an intelligent drug delivery system based on self-assembled two-dimensional peptide nanosheets (2D PNSs). Leveraging the tunable properties of amino acid structures and sequences, we design a peptide with the sequence of Fmoc-FKKGSHC, which self-assembles into 2D PNSs with uniform structure, high biocompatibility, and excellent degradability. Covalent attachment of thiol-modified doxorubicin (DOX) drugs to 2D PNSs via disulfide bond results in the peptide-drug conjugates (PDCs), which is denoted as PNS-SS-DOX. Subsequently, the PDCs are encapsulated within the injectable, thermosensitive chitosan (CS) hydrogels for drug delivery. The designed drug delivery system demonstrates outstanding pH-responsiveness and sustained drug release capabilities, which are facilitated by the characteristics of the CS hydrogels. Meanwhile, the covalently linked disulfide bond within the PNS-SS-DOX is responsive to intracellular glutathione (GSH) within tumor cells, enabling controlled drug release and significantly inhibiting the cancer cell growth. This responsive peptide-drug conjugate based on a 2D peptide nanoplatform paves the way for the development of smart drug delivery systems and has bright prospects in the future biomedicine field.

摘要

开发新型有效的药物输送系统,旨在增强治疗剂的治疗效果和疗效,是现代医学面临的一个关键挑战。本研究提出了一种基于自组装二维肽纳米片(2D PNSs)的智能药物输送系统。利用氨基酸结构和序列的可调特性,我们设计了一种具有 Fmoc-FKKGSHC 序列的肽,该肽自组装成具有均匀结构、高生物相容性和优异可降解性的 2D PNSs。通过二硫键将巯基修饰的阿霉素(DOX)药物共价连接到 2D PNSs 上,得到肽-药物缀合物(PDCs),记为 PNS-SS-DOX。随后,将 PDCs 包裹在可注射的、温敏性壳聚糖(CS)水凝胶中用于药物输送。设计的药物输送系统表现出出色的 pH 响应性和持续的药物释放能力,这得益于 CS 水凝胶的特性。同时,PNS-SS-DOX 中连接的二硫键对肿瘤细胞内的谷胱甘肽(GSH)有响应,能够实现控制药物释放,并显著抑制癌细胞生长。这种基于二维肽纳米平台的响应性肽-药物缀合物为智能药物输送系统的发展铺平了道路,在未来的生物医学领域具有广阔的前景。

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