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Gallium Maltolate Has Antiviral Activity Against SARS-CoV-2 and is a Potential Treatment for COVID-19

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Publisher Sage Publications
Date 2020 Dec 23
PMID 33353394
Citations 8
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Abstract

Background: Gallium has demonstrated strong anti-inflammatory activity in numerous animal studies, and has also demonstrated direct antiviral activity against the influenza A H1N1 virus and the human immunodeficiency virus (HIV). Gallium maltolate (GaM), a small metal-organic coordination complex, has been tested in several Phase 1 clinical trials, in which no dose-limiting or other serious toxicity was reported, even at high daily oral doses for several months at a time. For these reasons, GaM may be considered a potential candidate to treat coronavirus disease 2019 (COVID-19), which is caused by the SARS-CoV-2 virus and can result in severe, sometimes lethal, inflammatory reactions. In this study, we assessed the ability of GaM to inhibit the replication of SARS-CoV-2 in a culture of Vero E6 cells.

Methods: The efficacy of GaM in inhibiting the replication of SARS-CoV-2 was determined in a screening assay using cultured Vero E6 cells. The cytotoxicity of GaM in uninfected cells was determined using the Cell Counting Kit-8 (CCK-8) colorimetric assay.

Results: The results showed that GaM inhibits viral replication in a dose-dependent manner, with the concentration that inhibits replication by 50% (EC) being about 14 µM. No cytotoxicity was observed at concentrations up to at least 200 µM.

Conclusion: The activity of GaM against SARS-CoV-2, together with GaM's known anti-inflammatory activity, provide justification for testing GaM in COVID-19 patients.

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References
1.
Shepard D, Mullet D, Apseloff G, Weisbrode S, Gerber N . Gallium nitrate suppresses the production of nitric oxide and liver damage in a murine model of LPS-induced septic shock. Life Sci. 1999; 65(13):1359-71. DOI: 10.1016/s0024-3205(99)00375-6. View

2.
Bernstein L . Mechanisms of therapeutic activity for gallium. Pharmacol Rev. 1998; 50(4):665-82. View

3.
Bernstein L, Tanner T, Godfrey C, Noll B . Chemistry and pharmacokinetics of gallium maltolate, a compound with high oral gallium bioavailability. Met Based Drugs. 2008; 7(1):33-47. PMC: 2365198. DOI: 10.1155/MBD.2000.33. View

4.
Colafrancesco S, Alessandri C, Conti F, Priori R . COVID-19 gone bad: A new character in the spectrum of the hyperferritinemic syndrome?. Autoimmun Rev. 2020; 19(7):102573. PMC: 7199723. DOI: 10.1016/j.autrev.2020.102573. View

5.
Shang J, Wan Y, Luo C, Ye G, Geng Q, Auerbach A . Cell entry mechanisms of SARS-CoV-2. Proc Natl Acad Sci U S A. 2020; 117(21):11727-11734. PMC: 7260975. DOI: 10.1073/pnas.2003138117. View