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