铂类药物和水凝胶:一种前景广阔的抗肿瘤组合。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2023-12-01 Epub Date: 2023-12-11 DOI:10.1080/10717544.2023.2287966
Jiamin Yao, Shaojuan Song, Hang Zhao, Yao Yuan
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引用次数: 0

摘要

铂类药物被广泛用作一线抗肿瘤化疗药物。然而,由于药物在血液循环中游离,它们也有不可忽视的副作用。因此,有必要开发高效、安全的给药系统,以更好地靶向肿瘤细胞。水凝胶是一种很有前景的抗肿瘤药物载体,它可以形成铂金/水凝胶联合释药系统,在一些研究中显示出较好的抗肿瘤效果。然而,在这一领域缺乏系统的总结。本综述旨在通过以下几个部分对铂金/水凝胶组合系统进行全面概述:第一,介绍铂类药物;第二,分析铂金/水凝胶组合系统;第三,讨论基于水凝胶的给药系统的优势。我们希望这篇综述能为铂金/水凝胶组合系统的发展提供一些启示,以便更好地治疗癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Platinum-based drugs and hydrogel: a promising anti-tumor combination.

Platinum-based drugs are widely used as first-line anti-tumor chemotherapy agents. However, they also have nonnegligible side effects due to the free drugs in circulation. Therefore, it is necessary to develop efficient and safe delivery systems for better tumor cell targeting. Hydrogel is a promising anti-tumor drug carrier that can form a platinum/hydrogel combination system for drug release, which has shown better anti-tumor effects in some studies. However, there is a lack of systematic summary in this field. This review aims to provide a comprehensive overview of the platinum/hydrogel combination system with the following sections: firstly, an introduction of platinum-based drugs; secondly, an analysis of the platinum/hydrogel combination system; and thirdly, a discussion of the advantages of the hydrogel-based delivery system. We hope this review can offer some insights for the development of the platinum/hydrogel combination system for better cancer therapy.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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