多粘菌素B输送系统:提高抗菌活性和降低毒性的智能解决方案。

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Ying Cheng, Mingdong Yang, Bin Lin, Wei Hu, Yangmin Hu, Haibin Dai, Junjun Xu
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引用次数: 0

摘要

多粘菌素B (PMB)是治疗多重耐药革兰氏阴性细菌感染的最后一线药物。然而,由于其具有显著的肾毒性和神经毒性,其临床应用受到限制。近年来,智能给药系统已成为一个研究热点,旨在优化PMB的功能和治疗效果。本文系统综述了PMB的结构特点和抗菌机制,以及其在治疗耐药细菌感染方面面临的挑战。本文还讨论了PMB智能给药策略的进展,包括耐多药给药、抗生物膜技术、靶向给药、局部给药和协同治疗策略。这些策略通过增加局部药物浓度、降低毒性、增强抗菌谱和抑制耐药,为PMB的精确治疗提供了新的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymyxin B delivery systems: smart solutions for improved antibacterial activity and reduced toxicity.

Polymyxin B (PMB) serves as the last-line drug for treating multidrug-resistant Gram-negative bacterial infections. However, its clinical application is limited due to significant nephrotoxicity and neurotoxicity. In recent years, smart drug delivery systems have emerged as a research hotspot, aiming to optimise the functions and therapeutic effects of PMB. This article systematically reviews the structural characteristics and antibacterial mechanisms of PMB, as well as the challenges it faces in treating drug-resistant bacterial infections. The progress in smart delivery strategies for PMB is also discussed, including multidrug-resistant delivery, anti-biofilm technologies, targeted delivery, local administration, and synergistic treatment strategies. These strategies offer new directions for the precise treatment of PMB by increasing local drug concentration, reducing toxicity, enhancing the antibacterial spectrum, and inhibiting drug resistance.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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