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用于靶向抗菌递送以治疗传染病的传统脂质体修饰。

The modification of conventional liposomes for targeted antimicrobial delivery to treat infectious diseases.

作者信息

Okafor Nnamdi Ikemefuna, Omoteso Omobolanle Ayoyinka, Choonara Yahya E

机构信息

Wits Advanced Drug Delivery Platform Research Unit, Department of Pharmacy and Pharmacology, School of Therapeutic Sciences, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa.

Department of Pharmaceutics and Industrial Pharmacy, University of Ibadan, Ibadan, Nigeria.

出版信息

Discov Nano. 2025 Jan 30;20(1):19. doi: 10.1186/s11671-024-04170-x.

Abstract

Some of the most crucial turning points in the treatment strategies for some major infectious diseases including AIDS, malaria, and TB, have been reached with the introduction of antimicrobials and vaccines. Drug resistance and poor effectiveness are key limitations that need to be overcome. Conventional liposomes have been explored as a delivery system for infectious diseases bioactives to treat infectious diseases to provide an efficient approach to maximize the therapeutic outcomes, drug stability, targetability, to reduce the side-effects of antimicrobials, and enhance vaccine performance where necessary. However, as the pathological understanding of infectious diseases become more known, the need for more advanced liposomal technologies was born to continue having a profound effect on targeted chemotherapy for infectious diseases. This review therefore provides a concise incursion into the most recent and vogue liposomal formulations used to treat infectious diseases. An appraisal of immunological, stimuli-responsive, biomimetic and functionalized liposomes and other novel modifications to conventional liposomes is assimilated in sync with mutations of resistant pathogens.

摘要

随着抗菌药物和疫苗的引入,包括艾滋病、疟疾和结核病在内的一些主要传染病的治疗策略已达到一些最关键的转折点。耐药性和疗效不佳是需要克服的关键限制因素。传统脂质体已被探索作为传染病生物活性物质的递送系统,以治疗传染病,从而提供一种有效方法来最大化治疗效果、药物稳定性、靶向性,减少抗菌药物的副作用,并在必要时提高疫苗性能。然而,随着对传染病病理认识的不断深入,对更先进脂质体技术的需求应运而生,这将继续对传染病的靶向化疗产生深远影响。因此,本综述简要介绍了用于治疗传染病的最新和流行的脂质体制剂。结合耐药病原体的突变情况,对免疫脂质体、刺激响应脂质体、仿生脂质体、功能化脂质体以及对传统脂质体的其他新型修饰进行了评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/690f/11782757/bb65d9e4bf3a/11671_2024_4170_Fig1_HTML.jpg

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