In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2

The 2019 coronavirus infectious disease (COVID-19) is caused by infection with the new severe acute respiratory syndrome coronavirus (SARS-CoV-2). Currently, the treatment options for COVID-19 are limited. The purpose of the experiments presented here was to investigate the effectiveness of ketotife...

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Main Authors: Pantea Kiani, Andrew Scholey, Thomas A. Dahl, Lauren McMann, Jacqueline M. Iversen, Joris C. Verster
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/13/4/558
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spelling doaj-42207a123ca54024956404a8f5fd8cc82021-03-27T00:02:56ZengMDPI AGViruses1999-49152021-03-011355855810.3390/v13040558In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2Pantea Kiani0Andrew Scholey1Thomas A. Dahl2Lauren McMann3Jacqueline M. Iversen4Joris C. Verster5Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, 3584CG Utrecht, The NetherlandsCentre for Human Psychopharmacology, Swinburne University, Melbourne, VIC 3122, AustraliaSen-Jam Pharmaceutical, 223 Wall St., #130, Huntington, NY 11743, USASen-Jam Pharmaceutical, 223 Wall St., #130, Huntington, NY 11743, USASen-Jam Pharmaceutical, 223 Wall St., #130, Huntington, NY 11743, USADivision of Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, 3584CG Utrecht, The NetherlandsThe 2019 coronavirus infectious disease (COVID-19) is caused by infection with the new severe acute respiratory syndrome coronavirus (SARS-CoV-2). Currently, the treatment options for COVID-19 are limited. The purpose of the experiments presented here was to investigate the effectiveness of ketotifen, naproxen and indomethacin, alone or in combination, in reducing SARS-CoV-2 replication. In addition, the cytotoxicity of the drugs was evaluated. The findings showed that the combination of ketotifen with indomethacin (SJP-002C) or naproxen both reduce viral yield. Compared to ketotifen alone (60% inhibition at EC<sub>50</sub>), an increase in percentage inhibition of SARS-CoV-2 to 79%, 83% and 93% was found when co-administered with 25, 50 and 100 μM indomethacin, respectively. Compared to ketotifen alone, an increase in percentage inhibition of SARS-CoV-2 to 68%, 68% and 92% was found when co-administered with 25, 50 and 100 μM naproxen, respectively. For both drug combinations the observations suggest an additive or synergistic effect, compared to administering the drugs alone. No cytotoxic effects were observed for the administered dosages of ketotifen, naproxen, and indomethacin. Further research is warranted to investigate the efficacy of the combination of ketotifen with indomethacin (SJP-002C) or naproxen in the treatment of SARS-CoV-2 infection in humans.https://www.mdpi.com/1999-4915/13/4/558antiviraldrug repurposingSARS-CoV-2COVID-19SJP-002Cindomethacin
collection DOAJ
language English
format Article
sources DOAJ
author Pantea Kiani
Andrew Scholey
Thomas A. Dahl
Lauren McMann
Jacqueline M. Iversen
Joris C. Verster
spellingShingle Pantea Kiani
Andrew Scholey
Thomas A. Dahl
Lauren McMann
Jacqueline M. Iversen
Joris C. Verster
In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
Viruses
antiviral
drug repurposing
SARS-CoV-2
COVID-19
SJP-002C
indomethacin
author_facet Pantea Kiani
Andrew Scholey
Thomas A. Dahl
Lauren McMann
Jacqueline M. Iversen
Joris C. Verster
author_sort Pantea Kiani
title In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
title_short In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
title_full In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
title_fullStr In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
title_full_unstemmed In Vitro Assessment of the Antiviral Activity of Ketotifen, Indomethacin and Naproxen, Alone and in Combination, against SARS-CoV-2
title_sort in vitro assessment of the antiviral activity of ketotifen, indomethacin and naproxen, alone and in combination, against sars-cov-2
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2021-03-01
description The 2019 coronavirus infectious disease (COVID-19) is caused by infection with the new severe acute respiratory syndrome coronavirus (SARS-CoV-2). Currently, the treatment options for COVID-19 are limited. The purpose of the experiments presented here was to investigate the effectiveness of ketotifen, naproxen and indomethacin, alone or in combination, in reducing SARS-CoV-2 replication. In addition, the cytotoxicity of the drugs was evaluated. The findings showed that the combination of ketotifen with indomethacin (SJP-002C) or naproxen both reduce viral yield. Compared to ketotifen alone (60% inhibition at EC<sub>50</sub>), an increase in percentage inhibition of SARS-CoV-2 to 79%, 83% and 93% was found when co-administered with 25, 50 and 100 μM indomethacin, respectively. Compared to ketotifen alone, an increase in percentage inhibition of SARS-CoV-2 to 68%, 68% and 92% was found when co-administered with 25, 50 and 100 μM naproxen, respectively. For both drug combinations the observations suggest an additive or synergistic effect, compared to administering the drugs alone. No cytotoxic effects were observed for the administered dosages of ketotifen, naproxen, and indomethacin. Further research is warranted to investigate the efficacy of the combination of ketotifen with indomethacin (SJP-002C) or naproxen in the treatment of SARS-CoV-2 infection in humans.
topic antiviral
drug repurposing
SARS-CoV-2
COVID-19
SJP-002C
indomethacin
url https://www.mdpi.com/1999-4915/13/4/558
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