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  5. Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy?

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Article
en
2023

Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy?

0 Datasets

0 Files

en
2023
Vol 162
Vol. 162
DOI: 10.1016/j.biopha.2023.114367

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Michael R Hamblin
Michael R Hamblin

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Seyed Mohammad Reza Hashemian
Amirhossein Sheida
Mohammad Taghizadieh
+6 more

Abstract

Despite the need for novel, effective therapeutics for the COVID-19 pandemic, no curative regimen is yet available, therefore patients are forced to rely on supportive and nonspecific therapies. Some SARS-CoV-2 proteins, like the 3 C-like protease (3CLpro) or the major protease (Mpro), have been identified as promising targets for antiviral drugs. The Mpro has major a role in protein processing as well as pathogenesis of the virus, and could be a useful therapeutic target. The antiviral drug nirmatrelvir can keep SARS-CoV-2 from replicating through inhibiting Mpro. Nirmatrelvir was combined with another HIV protease inhibitor, ritonavir, to create Paxlovid (Nirmatrelvir/Ritonavir). The metabolizing enzyme cytochrome P450 3 A is inhibited by ritonavir to lengthen the half-life of nirmatrelvir, so rintonavir acts as a pharmacological enhancer. Nirmatrelvir exhibits potent antiviral activity against current coronavirus variants, despite significant alterations in the SARS-CoV-2 viral genome. Nevertheless, there are still several unanswered questions. This review summarizes the current literature on nirmatrelvir and ritonavir efficacy in treating SARS-CoV-2 infection, and also their safety and possible side effects.

How to cite this publication

Seyed Mohammad Reza Hashemian, Amirhossein Sheida, Mohammad Taghizadieh, Mohammad Yousef Memar, Michael R Hamblin, Hossein Bannazadeh Baghi, Javid Sadri Nahand, Zatollah Asemi, Hamed Mirzaei (2023). Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy?. , 162, DOI: https://doi.org/10.1016/j.biopha.2023.114367.

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Publication Details

Type

Article

Year

2023

Authors

9

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1016/j.biopha.2023.114367

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