治疗 COVID-19 的新型药物设计:临床前研究的系统回顾

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Canadian Journal of Infectious Diseases & Medical Microbiology Pub Date : 2022-09-25 eCollection Date: 2022-01-01 DOI:10.1155/2022/2044282
Sarah Mousavi, Shima Zare, Mahmoud Mirzaei, Awat Feizi
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引用次数: 0

摘要

背景:自新型冠状病毒(SARS-CoV-2)疾病爆发以来,人们对发现该疾病的潜在治疗药物越来越感兴趣。为此,我们对治疗 COVID-19 的药物开发(硅学、体外和体内)进行了系统回顾:从 2019 年 12 月到 2021 年 3 月,我们在主要数据库(包括 PubMed、Web of Science、Scopus、EMBASE 和 Google Scholar)中进行了系统检索。使用了以下术语组合:冠状病毒、COVID-19、SARS-CoV-2、药物设计、药物开发、硅学、体外和体内。对每项结果指标的数据综合采用了叙事综合法作为定性方法:结果:通过检索数据库,共发现了 2168 篇文章。最后,共纳入 315 项研究(266 项硅学研究、34 项体外研究和 15 项体内研究)。在采用硅学方法的研究中,98篇文章研究了COVID-19的再利用药物,91篇研究评估了草药。在通过计算方法重新确定用途的 260 种药物中,结果最好的是沙奎那韦(9 例)、利托那韦(8 例)和洛匹那韦(6 例)。主要蛋白酶(n = 154)、尖峰糖蛋白(n = 62)和病毒的其他非结构蛋白(n = 45)是研究最多的靶点。多西环素、氯丙嗪、阿奇霉素、肝素、贝普利地尔和甘草酸对 SARS-CoV-2 均有抑制作用:针对 COVID-19 的新型药物设计的临床前研究主要以主要蛋白酶和尖峰糖蛋白作为抗病毒开发的靶点。从评估的结构来看,硅学研究中的沙奎那韦、利托那韦、桉树、椴树、芦荟、绿茶、姜黄素、吡唑和三唑衍生物,体外研究中的多西环素、氯丙嗪和肝素,以及体内研究中的人类单克隆抗体都显示出了良好的疗效。看来,由于 COVID-19 疾病的性质,寻找一些具有多靶点抗病毒作用和抗炎潜力的药物是很有价值的,而一些草药就具有这种潜力。
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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Novel Drug Design for Treatment of COVID-19: A Systematic Review of Preclinical Studies.

Background: Since the beginning of the novel coronavirus (SARS-CoV-2) disease outbreak, there has been an increasing interest in discovering potential therapeutic agents for this disease. In this regard, we conducted a systematic review through an overview of drug development (in silico, in vitro, and in vivo) for treating COVID-19.

Methods: A systematic search was carried out in major databases including PubMed, Web of Science, Scopus, EMBASE, and Google Scholar from December 2019 to March 2021. A combination of the following terms was used: coronavirus, COVID-19, SARS-CoV-2, drug design, drug development, In silico, In vitro, and In vivo. A narrative synthesis was performed as a qualitative method for the data synthesis of each outcome measure.

Results: A total of 2168 articles were identified through searching databases. Finally, 315 studies (266 in silico, 34 in vitro, and 15 in vivo) were included. In studies with in silico approach, 98 article study repurposed drug and 91 studies evaluated herbal medicine on COVID-19. Among 260 drugs repurposed by the computational method, the best results were observed with saquinavir (n = 9), ritonavir (n = 8), and lopinavir (n = 6). Main protease (n = 154) following spike glycoprotein (n = 62) and other nonstructural protein of virus (n = 45) was among the most studied targets. Doxycycline, chlorpromazine, azithromycin, heparin, bepridil, and glycyrrhizic acid showed both in silico and in vitro inhibitory effects against SARS-CoV-2.

Conclusion: The preclinical studies of novel drug design for COVID-19 focused on main protease and spike glycoprotein as targets for antiviral development. From evaluated structures, saquinavir, ritonavir, eucalyptus, Tinospora cordifolia, aloe, green tea, curcumin, pyrazole, and triazole derivatives in in silico studies and doxycycline, chlorpromazine, and heparin from in vitro and human monoclonal antibodies from in vivo studies showed promised results regarding efficacy. It seems that due to the nature of COVID-19 disease, finding some drugs with multitarget antiviral actions and anti-inflammatory potential is valuable and some herbal medicines have this potential.

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
108
审稿时长
>12 weeks
期刊介绍: Canadian Journal of Infectious Diseases and Medical Microbiology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to infectious diseases of bacterial, viral and parasitic origin. The journal welcomes articles describing research on pathogenesis, epidemiology of infection, diagnosis and treatment, antibiotics and resistance, and immunology.
期刊最新文献
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