重新利用Poloxamers作为抗菌剂:机制和应用的综合综述

IF 3.5 4区 医学 Q2 CHEMISTRY, MEDICINAL
Sheila I. Peña Corona, Fabiola V. Borbolla-Jiménez, Lorena Duarte-Peña, Angélica Moreno, Luis E. Pérez-Caltzontzin, María Luisa Del Prado-Audelo, Alejandra Romero-Montero, Maykel González-Torres, Hernán Cortés, Hector Hernández-Parra, Javad Sharifi-Rad, Gerardo Leyva-Gómez
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引用次数: 0

摘要

在过去几十年中,误用和过度使用抗微生物药物加速了抗微生物药物耐药性的出现,这一现象与全世界每年约495万人死亡有关。控制这种耐药性是抗菌素疗法和新型药物制剂面临的最大挑战。Poloxamers是一种非离子合成三嵌段共聚物,用作配制抗生素的赋形剂,主要用作乳化剂、胶凝剂、表面活性剂和湿润剂。研究发现,poloxamers可能作为杀微生物剂或微生物抑制剂具有抗菌活性,也可以增强其他杀菌药物的功效。本文综述了poloxamers作为抗菌药物治疗微生物感染的潜在作用机制。本综述的方法包括从PubMed、b谷歌Scholar和Scopus中获取文章,使用特定的医学主题标题来保证准确性和针对性。波洛沙姆的作用机制包括群体感应抑制、细胞膜破坏、细菌生物膜抑制和细菌细胞壁破坏。分子对接的结果表明,poloxamers可以直接与粘附蛋白的活性位点相互作用并改变其功能。实验结果表明,poloxamers 188和407可以有效抑制金黄色葡萄球菌和铜绿假单胞菌的生长,具有抗菌潜力。尽管有令人信服的证据,但需要进一步的研究来克服与泊洛沙莫的生物利用度有关的挑战,并为不同的泊洛沙莫建立有效的给药方案,以保证其作为抗菌药物的使用和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repurposing Poloxamers as Antimicrobial Agents: A Comprehensive Review of Mechanisms and Applications

In the last decades, the misuse and overuse of antimicrobial medications have precipitated the appearance of antimicrobial resistance, a phenomenon associated with around 4.95 million deaths per year worldwide. Control of this resistance represents the biggest challenge for antimicrobial therapies and novel drug formulations. Poloxamers are nonionic synthetic triblock copolymers used as excipients for formulating antibiotics, mainly as emulsifying agents, gelling agents, surfactants, and humectants. It has been discovered that poloxamers may have antimicrobial activity as microbicides or micro biostatics or can also potentiate other germicide drugs' efficacy. This review aims to examine the use of poloxamers and synthesize their potential mechanisms of action as antimicrobial drugs for treating microbial infections. This review's methodology included sourcing articles from PubMed, Google Scholar, and Scopus, using specific medical subject headings terms to warranty precision and pertinence. Poloxamer action mechanisms include quorum sensing inhibition, cellular membrane disruption, bacterial biofilm inhibition, and disruptions in bacteria cell walls. Results of Molecular docking demonstrated that poloxamers could interact directly with active sites of adhesion proteins and alter their functioning. Our experimental tests showed that poloxamers 188 and 407 possess the potential to be antimicrobial agents by effectively inhibiting Staphylococcus aureus and Pseudomonas aeruginosa growth. Despite the convincing evidence, further research is required to overcome challenges related to poloxamers' bioavailability and establish effective dosing regimens for different poloxamers to warrant their use and safety as antimicrobial drugs.

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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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