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改善抗癌药物治疗的功能配体:现状和在药物传递系统中的应用。

Functional ligands for improving anticancer drug therapy: current status and applications to drug delivery systems.

机构信息

College of Pharmacy, Dongguk University-Seoul, Goyang, Korea.

出版信息

Drug Deliv. 2022 Dec;29(1):1959-1970. doi: 10.1080/10717544.2022.2089296.

Abstract

Conventional chemotherapy lacking target selectivity often leads to severe side effects, limiting the effectiveness of chemotherapy. Therefore, drug delivery systems ensuring both selective drug release and efficient intracellular uptake at the target sites are highly demanded in chemotherapy to improve the quality of life of patients with low toxicity. One of the effective approaches for tumor-selective drug delivery is the adoption of functional ligands that can interact with specific receptors overexpressed in malignant cancer cells. Various functional ligands including folic acid, hyaluronic acid, transferrin, peptides, and antibodies, have been extensively explored to develop tumor-selective drug delivery systems. Furthermore, cell-penetrating peptides or ligands for tight junction opening are also actively pursued to improve the intracellular trafficking of anticancer drugs. Sometimes, multiple ligands with different roles are used in combination to enhance the cellular uptake as well as target selectivity of anticancer drugs. In this review, the current status of various functional ligands applicable to improve the effectiveness of cancer chemotherapy is overviewed with a focus on their roles, characteristics, and preclinical/clinical applications.

摘要

传统的化疗缺乏靶向选择性,往往会导致严重的副作用,限制了化疗的效果。因此,在化疗中需要能够确保药物在靶部位选择性释放和高效细胞内摄取的药物递送系统,以提高低毒性患者的生活质量。肿瘤选择性药物递送的有效方法之一是采用能够与恶性癌细胞中过度表达的特定受体相互作用的功能配体。已经广泛探索了各种功能配体,包括叶酸、透明质酸、转铁蛋白、肽和抗体,以开发肿瘤选择性药物递送系统。此外,还积极研究细胞穿透肽或用于紧密连接开放的配体,以改善抗癌药物的细胞内转运。有时,将具有不同作用的多种配体联合使用,以增强抗癌药物的细胞摄取和靶向选择性。在本文中,我们综述了各种适用于提高癌症化疗效果的功能配体的最新研究进展,重点介绍了它们的作用、特性和临床前/临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74a2/9246174/5af9d772f524/IDRD_A_2089296_F0001_C.jpg

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