Suppr超能文献

用于治疗新冠肺炎的新型药物设计:临床前研究的系统综述

Novel Drug Design for Treatment of COVID-19: A Systematic Review of Preclinical Studies.

作者信息

Mousavi Sarah, Zare Shima, Mirzaei Mahmoud, Feizi Awat

机构信息

Department of Clinical Pharmacy and Pharmacy Practice, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Can J Infect Dis Med Microbiol. 2022 Sep 25;2022:2044282. doi: 10.1155/2022/2044282. eCollection 2022.

Abstract

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 ( = 9), ritonavir ( = 8), and lopinavir ( = 6). Main protease ( = 154) following spike glycoprotein ( = 62) and other nonstructural protein of virus ( = 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.

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的兴趣与日俱增。在这方面,我们通过对治疗新冠肺炎的药物研发(计算机模拟、体外和体内)进行综述,开展了一项系统评价。

方法

于2019年12月至2021年3月在主要数据库中进行系统检索,包括PubMed、科学网、Scopus、EMBASE和谷歌学术。使用了以下术语的组合:冠状病毒、新冠肺炎、SARS-CoV-2、药物设计、药物研发、计算机模拟、体外和体内。采用叙述性综合作为一种定性方法,对每个结局指标的数据进行综合分析。

结果

通过检索数据库共识别出2168篇文章。最终纳入315项研究(266项计算机模拟研究、34项体外研究和15项体内研究)。在计算机模拟研究中,98篇文章研究了药物重新利用,91项研究评估了草药对新冠肺炎的作用。在通过计算方法重新利用的260种药物中,沙奎那韦(得分=9)、利托那韦(得分=8)和洛匹那韦(得分=6)的效果最佳。主要蛋白酶(得分=154)是研究最多的靶点之一,其次是刺突糖蛋白(得分=62)和病毒的其他非结构蛋白(得分=45)。多西环素、氯丙嗪、阿奇霉素、肝素、苄普地尔和甘草酸在计算机模拟和体外实验中均显示出对SARS-CoV-2的抑制作用。

结论

新冠肺炎新药设计的临床前研究主要聚焦于将主要蛋白酶和刺突糖蛋白作为抗病毒研发的靶点。从评估的结构来看,计算机模拟研究中的沙奎那韦、利托那韦、桉树叶、心叶青牛胆、芦荟、绿茶、姜黄素、吡唑和三唑衍生物,以及体外研究中的多西环素、氯丙嗪和肝素,还有体内研究中的人单克隆抗体,在疗效方面均显示出有前景的结果。由于新冠肺炎疾病的特性,找到一些具有多靶点抗病毒作用和抗炎潜力的药物很有价值,一些草药具有这种潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f70/9527439/becdad0321e7/CJIDMM2022-2044282.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验