Self-responsive biomimetic short lipopeptide-based delivery systems for enhanced antibiotic efficacy against drug-resistant infections.

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shruti Sharma, Deepanshi Saxena, Aanand Kautu, Sidharth Chopra, Khashti Ballabh Joshi
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引用次数: 0

Abstract

Biocompatible short peptide amphiphile nanostructures were developed as an innovative platform for the efficient delivery of meropenem. These nanostructures exhibit self-responsive behavior, specifically targeting infection sites and releasing the antibiotic in a controlled manner. Testing against clinically relevant bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Staphylococcus aureus (VRSA), demonstrated their ability to enhance antibiotic concentration at the site of infection, significantly improving therapeutic efficacy. By reducing the required dosages, this approach minimizes systemic cytotoxicity and mitigates the side effects associated with higher drug concentrations. The study highlights the potential of these nanostructures as a promising strategy to combat drug-resistant bacterial infections, addressing a critical global health challenge.

基于自我反应的仿生短脂肽输送系统,用于增强抗生素对耐药感染的疗效。
生物相容性短肽两亲性纳米结构被开发为有效递送美罗培南的创新平台。这些纳米结构表现出自响应行为,专门针对感染部位并以可控的方式释放抗生素。对临床相关细菌,包括耐甲氧西林金黄色葡萄球菌(MRSA)和耐万古霉素金黄色葡萄球菌(VRSA)的检测表明,它们能够提高感染部位的抗生素浓度,显著提高治疗效果。通过减少所需的剂量,这种方法最大限度地减少了全身细胞毒性,减轻了与较高药物浓度相关的副作用。这项研究强调了这些纳米结构作为对抗耐药细菌感染的一种有希望的策略的潜力,解决了一个关键的全球健康挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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