Related Experiment Video
Updated: Nov 13, 2025

Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
Hemoadsorption eliminates remdesivir from the circulation: Implications for the treatment of COVID-19
Paul Biever1,2,3, Dawid L Staudacher1,2, Michaela J Sommer4,5
1Heart Center Freiburg University, Department of Cardiology and Angiology I, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Insights
The CytoSorb device significantly removes remdesivir and its active metabolite GS-441524 from blood in vitro. Simultaneous use of remdesivir and CytoSorb therapy in severe COVID-19 patients is not recommended due to drug elimination.
Area of Science:
- Pharmacology
- Critical Care Medicine
- Biomedical Engineering
Background:
- Severe COVID-19 treatment involves antiviral remdesivir and hemoadsorption with CytoSorb.
- CytoSorb adsorbs various molecules, including cytokines and drugs.
- Potential drug-device interactions require investigation.
Purpose of the Study:
- To evaluate the adsorption of remdesivir and its metabolite GS-441524 by the CytoSorb device in vitro.
- To determine the impact of CytoSorb on remdesivir and GS-441524 concentrations.
Main Methods:
- Serum containing remdesivir or GS-441524 was circulated through a CytoSorb device in a custom system.
- Drug concentrations were analyzed using liquid chromatography-tandem mass spectrometry.
- Pre- and post-adsorber concentrations were measured to assess removal efficiency.
Main Results:
- CytoSorb rapidly and almost completely removed remdesivir from the perfusate within 60 minutes.
- GS-441524 showed similar rapid elimination, reaching an adsorption-desorption equilibrium around 48 µg/L.
- Both remdesivir and GS-441524 were significantly reduced by the CytoSorb device in vitro.
Conclusions:
- Remdesivir and its active metabolite GS-441524 are effectively eliminated by the CytoSorb adsorber.
- Concurrent use of remdesivir and CytoSorb in patients should be avoided.
- Close monitoring of therapeutic drug plasma levels during CytoSorb therapy is crucial.
Abstract:
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.
Related Concept Videos
Extracorporeal Removal of Drugs: Hemoperfusion and Hemofiltration
Extracorporeal Removal of Drugs: Continuous Renal Replacement Therapy
Extracorporeal Removal of Drugs: Peritoneal Dialysis and Hemodialysis
Retrovirus Life Cycles
Enhanced Elimination of Poison
Antidotes serve a crucial role in counteracting the effects of poison by inhibiting enzymes responsible for producing harmful drug metabolites. In some cases, these toxic metabolites can be neutralized by endogenous cosubstrates, which are maintained at specific concentrations to prevent interaction with cellular macromolecules and subsequent cell death.
Renal excretion is the...
Pharmacokinetics: Drug–Food and Drug–Viral Interactions

