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Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19
Both antiviral treatment with remdesivir and hemoadsorption using a CytoSorb(®) adsorption device are applied in the treatment of severe COVID‐19. The CytoSorb(®) adsorber consists of porous polymer beads that adsorb a broad range of molecules, including cytokines but also several therapeutic drugs....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953359/ https://www.ncbi.nlm.nih.gov/pubmed/33710753 http://dx.doi.org/10.1002/prp2.743 |
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author | Biever, Paul Staudacher, Dawid L. Sommer, Michaela J. Triebel, Hannah Neukamm, Merja A. Bode, Christoph Supady, Alexander Lother, Achim |
author_facet | Biever, Paul Staudacher, Dawid L. Sommer, Michaela J. Triebel, Hannah Neukamm, Merja A. Bode, Christoph Supady, Alexander Lother, Achim |
author_sort | Biever, Paul |
collection | PubMed |
description | Both antiviral treatment with remdesivir and hemoadsorption using a CytoSorb(®) adsorption device are applied in the treatment of severe COVID‐19. The CytoSorb(®) adsorber consists of porous polymer beads that adsorb a broad range of molecules, including cytokines but also several therapeutic drugs. In this study, we evaluated whether remdesivir and its main active metabolite GS‐441524 would be adsorbed by CytoSorb(®). Serum containing remdesivir or GS‐441524 was circulated in a custom‐made system containing a CytoSorb(®) device. Concentrations of remdesivir and GS‐441524 before and after the adsorber were analyzed by liquid chromatography‐tandem mass spectrometry. Measurements of remdesivir in the outgoing tube after the adsorber indicated almost complete removal of remdesivir by the device. In the reservoir, concentration of remdesivir showed an exponential decay and was not longer detectable after 60 mins. GS‐441524 showed a similar exponential decay but, unlike remdesivir, it reached an adsorption–desorption equilibrium at ~48 µg/L. Remdesivir and its main active metabolite GS‐441524 are rapidly eliminated from the perfusate by the CytoSorb(®) adsorber device in vitro. This should be considered in patients for whom both therapies are indicated, and simultaneous application should be avoided. In general, plasma levels of therapeutic drugs should be closely monitored under concurrent CytoSorb(®) therapy. |
format | Online Article Text |
id | pubmed-7953359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79533592021-03-17 Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 Biever, Paul Staudacher, Dawid L. Sommer, Michaela J. Triebel, Hannah Neukamm, Merja A. Bode, Christoph Supady, Alexander Lother, Achim Pharmacol Res Perspect Short Report Both antiviral treatment with remdesivir and hemoadsorption using a CytoSorb(®) adsorption device are applied in the treatment of severe COVID‐19. The CytoSorb(®) adsorber consists of porous polymer beads that adsorb a broad range of molecules, including cytokines but also several therapeutic drugs. In this study, we evaluated whether remdesivir and its main active metabolite GS‐441524 would be adsorbed by CytoSorb(®). Serum containing remdesivir or GS‐441524 was circulated in a custom‐made system containing a CytoSorb(®) device. Concentrations of remdesivir and GS‐441524 before and after the adsorber were analyzed by liquid chromatography‐tandem mass spectrometry. Measurements of remdesivir in the outgoing tube after the adsorber indicated almost complete removal of remdesivir by the device. In the reservoir, concentration of remdesivir showed an exponential decay and was not longer detectable after 60 mins. GS‐441524 showed a similar exponential decay but, unlike remdesivir, it reached an adsorption–desorption equilibrium at ~48 µg/L. Remdesivir and its main active metabolite GS‐441524 are rapidly eliminated from the perfusate by the CytoSorb(®) adsorber device in vitro. This should be considered in patients for whom both therapies are indicated, and simultaneous application should be avoided. In general, plasma levels of therapeutic drugs should be closely monitored under concurrent CytoSorb(®) therapy. John Wiley and Sons Inc. 2021-03-12 /pmc/articles/PMC7953359/ /pubmed/33710753 http://dx.doi.org/10.1002/prp2.743 Text en © 2021 The Authors. Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Short Report Biever, Paul Staudacher, Dawid L. Sommer, Michaela J. Triebel, Hannah Neukamm, Merja A. Bode, Christoph Supady, Alexander Lother, Achim Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title | Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title_full | Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title_fullStr | Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title_full_unstemmed | Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title_short | Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID‐19 |
title_sort | hemoadsorption eliminates remdesivir from the circulation: implications for the treatment of covid‐19 |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953359/ https://www.ncbi.nlm.nih.gov/pubmed/33710753 http://dx.doi.org/10.1002/prp2.743 |
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