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抗病毒治疗的革命:揭示增强药物疗效的创新方法。

Revolutionizing Antiviral Therapeutics: Unveiling Innovative Approaches for Enhanced Drug Efficacy.

机构信息

Department of Pharmaceutical Analysis and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran, Sumedang, 45363, Indonesia.

Research Collaboration Centre for Theranostic Radio Pharmaceuticals, National Research and Innovation Agency (BRIN), Sumedang, 45363, Indonesia.

出版信息

Int J Nanomedicine. 2024 Mar 20;19:2889-2915. doi: 10.2147/IJN.S447721. eCollection 2024.

Abstract

Since the beginning of the coronavirus pandemic in late 2019, viral infections have become one of the top three causes of mortality worldwide. Immunization and the use of immunomodulatory drugs are effective ways to prevent and treat viral infections. However, the primary therapy for managing viral infections remains antiviral and antiretroviral medication. Unfortunately, these drugs are often limited by physicochemical constraints such as low target selectivity and poor aqueous solubility. Although several modifications have been made to enhance the physicochemical characteristics and efficacy of these drugs, there are few published studies that summarize and compare these modifications. Our review systematically synthesized and discussed antiviral drug modification reports from publications indexed in Scopus, PubMed, and Google Scholar databases. We examined various approaches that were investigated to address physicochemical issues and increase activity, including liposomes, cocrystals, solid dispersions, salt modifications, and nanoparticle drug delivery systems. We were impressed by how well each strategy addressed physicochemical issues and improved antiviral activity. In conclusion, these modifications represent a promising way to improve the physicochemical characteristics, functionality, and effectiveness of antivirals in clinical therapy.

摘要

自 2019 年末冠状病毒大流行以来,病毒感染已成为全球三大死亡原因之一。免疫接种和使用免疫调节剂是预防和治疗病毒感染的有效方法。然而,管理病毒感染的主要治疗方法仍然是抗病毒和抗逆转录病毒药物。不幸的是,这些药物通常受到物理化学限制的限制,例如低靶选择性和差的水溶解度。尽管已经对这些药物进行了多种修饰以增强其物理化学特性和功效,但很少有发表的研究对这些修饰进行总结和比较。我们的综述系统地综合和讨论了 Scopus、PubMed 和 Google Scholar 数据库中索引的出版物中有关抗病毒药物修饰的报告。我们研究了各种方法来解决物理化学问题并提高活性,包括脂质体、共晶、固体分散体、盐修饰和纳米颗粒药物递送系统。我们对每种策略解决物理化学问题和提高抗病毒活性的效果印象深刻。总之,这些修饰代表了改善抗病毒药物在临床治疗中的物理化学特性、功能和效果的有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5a1/10961067/325cfce043cb/IJN-19-2889-g0001.jpg

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