纳米给药系统抗多药耐药性研究进展

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Changduo Wang, Fashun Li, Tianao Zhang, Min Yu, Yong Sun
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引用次数: 0

摘要

摘要肿瘤化疗偶尔会产生耐药性,这是导致治疗失败的主要原因。较高的药物剂量可以提高治疗效果,但较高的毒性限制了进一步的治疗。为了克服耐药性,人们已经探索了功能性纳米给药系统(NDDS)来敏化抗癌药物并降低其副作用,该系统通过绕过药物外排、控制药物释放和干扰代谢等多种机制应用于对抗多药耐药性(MDR)。本综述从主要MDR原因的简要报告开始。此外,我们检索了NDDS的论文,并介绍了化疗药物对MDR肿瘤增敏的最新进展。最后,我们得出结论,NDDS基于几种机制,并展望了该领域的未来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent advances in anti-multidrug resistance for nano-drug delivery system.

Chemotherapy for tumors occasionally results in drug resistance, which is the major reason for the treatment failure. Higher drug doses could improve the therapeutic effect, but higher toxicity limits the further treatment. For overcoming drug resistance, functional nano-drug delivery system (NDDS) has been explored to sensitize the anticancer drugs and decrease its side effects, which are applied in combating multidrug resistance (MDR) via a variety of mechanisms including bypassing drug efflux, controlling drug release, and disturbing metabolism. This review starts with a brief report on the major MDR causes. Furthermore, we searched the papers from NDDS and introduced the recent advances in sensitizing the chemotherapeutic drugs against MDR tumors. Finally, we concluded that the NDDS was based on several mechanisms, and we looked forward to the future in this field.

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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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