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Erschienen in: Clinical Pharmacokinetics 7/2017

02.12.2016 | Original Research Article

Effect of Activated Charcoal on Rivaroxaban Complex Absorption

verfasst von: Edouard Ollier, Sophie Hodin, Julien Lanoiselée, Jean Escal, Sandrine Accassat, Elodie De Magalhaes, Thierry Basset, Laurent Bertoletti, Patrick Mismetti, Xavier Delavenne

Erschienen in: Clinical Pharmacokinetics | Ausgabe 7/2017

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Abstract

Objective

To quantify the impact of activated charcoal (AC) on rivaroxaban exposure in healthy volunteers.

Methods

This was an open-label study with an incomplete cross-over design of single-dose rivaroxaban (40 mg) administered alone or with AC in 12 healthy volunteers. The study comprised three treatment periods in randomised sequence, one with rivaroxaban administered alone and two with AC given at 2, 5 or 8 h post-dose. Rivaroxaban plasma concentration was measured in blood samples drawn at 16 time points. The pharmacokinetic model of rivaroxaban alone or with AC administration was built using a non-linear mixed-effect modelling approach.

Results

The pharmacokinetic model was based on a one-compartment model with an absorption rate described by the sum of three inverse Gaussian densities to reproduce multiphasic and prolonged absorption. The inclusion in the model of each AC administration schedule significantly improved objective function value. AC reduced the area under the rivaroxaban concentration-time curve by 43% when administered 2 h post-dose, by 31% when administered 5 h post-dose and by 29% when administered 8 h post-dose. Based on the estimated pharmacokinetic model, simulations suggested that AC might have an impact even after 8 h post-dose.

Conclusion

AC administration significantly reduces exposure to rivaroxaban even if AC is administered 8 h after rivaroxaban. These results suggest that AC could be used in rivaroxaban overdose and accidental ingestion to antagonise absorption.

ClinicalTrial.gov registration no.

NCT02657512.
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Literatur
1.
Zurück zum Zitat Ruff CT, Giugliano RP, Braunwald E, et al. Comparison of the efficacy and safety of new oral anticoagulants with warfarin in patients with atrial fibrillation: a meta-analysis of randomised trials. Lancet. 2014;383:955–62.CrossRefPubMed Ruff CT, Giugliano RP, Braunwald E, et al. Comparison of the efficacy and safety of new oral anticoagulants with warfarin in patients with atrial fibrillation: a meta-analysis of randomised trials. Lancet. 2014;383:955–62.CrossRefPubMed
2.
Zurück zum Zitat Juurlink DN. Activated charcoal for acute overdose: a reappraisal. Br J Clin Pharmacol. 2016;81:482–7.CrossRefPubMed Juurlink DN. Activated charcoal for acute overdose: a reappraisal. Br J Clin Pharmacol. 2016;81:482–7.CrossRefPubMed
3.
Zurück zum Zitat Cooper JM, Duffull SB, Saiao AS, Isbister GK. The pharmacokinetics of sertraline in overdose and the effect of activated charcoal. Br J Clin Pharmacol. 2015;79:307–15.CrossRefPubMedPubMedCentral Cooper JM, Duffull SB, Saiao AS, Isbister GK. The pharmacokinetics of sertraline in overdose and the effect of activated charcoal. Br J Clin Pharmacol. 2015;79:307–15.CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Weinz C, Schwarz T, Kubitza D, et al. Metabolism and excretion of rivaroxaban, an oral, direct factor Xa inhibitor, in rats, dogs, and humans. Drug Metab Dispos. 2009;37:1056–64.CrossRefPubMed Weinz C, Schwarz T, Kubitza D, et al. Metabolism and excretion of rivaroxaban, an oral, direct factor Xa inhibitor, in rats, dogs, and humans. Drug Metab Dispos. 2009;37:1056–64.CrossRefPubMed
7.
Zurück zum Zitat Schmitz EM, Boonen K, van den Heuvel DJ, et al. Determination of dabigatran, rivaroxaban and apixaban by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) and coagulation assays for therapy monitoring of novel direct oral anticoagulants. J Thromb Haemost. 2014;12:1636–46.CrossRefPubMed Schmitz EM, Boonen K, van den Heuvel DJ, et al. Determination of dabigatran, rivaroxaban and apixaban by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) and coagulation assays for therapy monitoring of novel direct oral anticoagulants. J Thromb Haemost. 2014;12:1636–46.CrossRefPubMed
9.
Zurück zum Zitat Kuhn E, Lavielle M. Coupling a stochastic approximation version of EM with an MCMC procedure. ESAIM Prob Stat. 2004;8:115–31.CrossRef Kuhn E, Lavielle M. Coupling a stochastic approximation version of EM with an MCMC procedure. ESAIM Prob Stat. 2004;8:115–31.CrossRef
10.
Zurück zum Zitat Samson A, Lavielle M, Mentré F. Extension of the SAEM algorithm to left-censored data in nonlinear mixed-effects model: application to HIV dynamics model. Comput Stat Data Anal. 2006;51:1562–74.CrossRef Samson A, Lavielle M, Mentré F. Extension of the SAEM algorithm to left-censored data in nonlinear mixed-effects model: application to HIV dynamics model. Comput Stat Data Anal. 2006;51:1562–74.CrossRef
11.
Zurück zum Zitat Wickham H. ggplot2: elegant graphics for data analysis. New York: Springer; 2009.CrossRef Wickham H. ggplot2: elegant graphics for data analysis. New York: Springer; 2009.CrossRef
12.
Zurück zum Zitat R Development Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria, 2013. http://www.R-project.org. Accessed 15 Jun 2016. R Development Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria, 2013. http://​www.​R-project.​org. Accessed 15 Jun 2016.
13.
Zurück zum Zitat Csajka C, Drover D, Verotta D. The use of a sum of inverse Gaussian functions to describe the absorption profile of drugs exhibiting complex absorption. Pharm Res. 2005;22:1227–35.CrossRefPubMed Csajka C, Drover D, Verotta D. The use of a sum of inverse Gaussian functions to describe the absorption profile of drugs exhibiting complex absorption. Pharm Res. 2005;22:1227–35.CrossRefPubMed
14.
Zurück zum Zitat Shivva V, Korell J, Tucker IG, Duffull SB. An approach for identifiability of population pharmacokinetic-pharmacodynamic models. CPT Pharmacomet Syst Pharmacol. 2013;2:1–9.CrossRef Shivva V, Korell J, Tucker IG, Duffull SB. An approach for identifiability of population pharmacokinetic-pharmacodynamic models. CPT Pharmacomet Syst Pharmacol. 2013;2:1–9.CrossRef
15.
Zurück zum Zitat Lavielle M, Aarons L. What do we mean by identifiability in mixed effects models? J Pharmacokinet Pharmacodyn. 2016;43:111–22.CrossRefPubMed Lavielle M, Aarons L. What do we mean by identifiability in mixed effects models? J Pharmacokinet Pharmacodyn. 2016;43:111–22.CrossRefPubMed
16.
Zurück zum Zitat Weiss M, Sermsappasuk P, Siegmund W. Modeling the kinetics of digoxin absorption: enhancement by P-glycoprotein inhibition. J Clin Pharmacol. 2012;52:381–7.CrossRefPubMed Weiss M, Sermsappasuk P, Siegmund W. Modeling the kinetics of digoxin absorption: enhancement by P-glycoprotein inhibition. J Clin Pharmacol. 2012;52:381–7.CrossRefPubMed
17.
Zurück zum Zitat Stampfuss J, Kubitza D, Becka M, Mueck W. The effect of food on the absorption and pharmacokinetics of rivaroxaban. Int J Clin Pharmacol Ther. 2013;51:549–61.CrossRefPubMed Stampfuss J, Kubitza D, Becka M, Mueck W. The effect of food on the absorption and pharmacokinetics of rivaroxaban. Int J Clin Pharmacol Ther. 2013;51:549–61.CrossRefPubMed
19.
Zurück zum Zitat Wang X, Mondal S, Wang J, et al. Effect of activated charcoal on apixaban pharmacokinetics in healthy subjects. Am J Cardiovasc Drugs. 2014;14:147–54.CrossRefPubMed Wang X, Mondal S, Wang J, et al. Effect of activated charcoal on apixaban pharmacokinetics in healthy subjects. Am J Cardiovasc Drugs. 2014;14:147–54.CrossRefPubMed
20.
Zurück zum Zitat Wendling T, Ogungbenro K, Pigeolet E, et al. Model-based evaluation of the impact of formulation and food intake on the complex oral absorption of mavoglurant in healthy subjects. Pharm Res. 2015;32:1764–78.CrossRefPubMed Wendling T, Ogungbenro K, Pigeolet E, et al. Model-based evaluation of the impact of formulation and food intake on the complex oral absorption of mavoglurant in healthy subjects. Pharm Res. 2015;32:1764–78.CrossRefPubMed
21.
Zurück zum Zitat Ollier E, Hodin S, Basset T, et al. In vitro and in vivo evaluation of drug-drug interaction between dabigatran and proton pump inhibitors. Fundam Clin Pharmacol. 2015;29:604–14.CrossRefPubMed Ollier E, Hodin S, Basset T, et al. In vitro and in vivo evaluation of drug-drug interaction between dabigatran and proton pump inhibitors. Fundam Clin Pharmacol. 2015;29:604–14.CrossRefPubMed
22.
Zurück zum Zitat Mueck W, Becka M, Kubitza D, et al. Population model of the pharmacokinetics and pharmacodynamics of rivaroxaban an oral, direct factor Xa inhibitor in healthy subjects. Int J Clin Pharmacol Ther. 2007;45:335–44.CrossRefPubMed Mueck W, Becka M, Kubitza D, et al. Population model of the pharmacokinetics and pharmacodynamics of rivaroxaban an oral, direct factor Xa inhibitor in healthy subjects. Int J Clin Pharmacol Ther. 2007;45:335–44.CrossRefPubMed
23.
Zurück zum Zitat Mueck W, Kubitza D, Becka M. Co-administration of rivaroxaban with drugs that share its elimination pathways: pharmacokinetic effects in healthy subjects. Br J Clin Pharmacol. 2013;76:455–66.CrossRefPubMedPubMedCentral Mueck W, Kubitza D, Becka M. Co-administration of rivaroxaban with drugs that share its elimination pathways: pharmacokinetic effects in healthy subjects. Br J Clin Pharmacol. 2013;76:455–66.CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Mueck W, Borris LC, Dahl OE, et al. Population pharmacokinetics and pharmacodynamics of once- and twice-daily rivaroxaban for the prevention of venous thromboembolism in patients undergoing total hip replacement. Thromb Haemost. 2008;100:453–61.PubMed Mueck W, Borris LC, Dahl OE, et al. Population pharmacokinetics and pharmacodynamics of once- and twice-daily rivaroxaban for the prevention of venous thromboembolism in patients undergoing total hip replacement. Thromb Haemost. 2008;100:453–61.PubMed
25.
Zurück zum Zitat Xu XS, Moore K, Burton P, et al. Population pharmacokinetics and pharmacodynamics of rivaroxaban in patients with acute coronary syndromes. Br J Clin Pharmacol. 2012;74:86–97.CrossRefPubMedPubMedCentral Xu XS, Moore K, Burton P, et al. Population pharmacokinetics and pharmacodynamics of rivaroxaban in patients with acute coronary syndromes. Br J Clin Pharmacol. 2012;74:86–97.CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Siegal DM, Curnutte JT, Connolly SJ, et al. Andexanet alfa for the reversal of factor Xa inhibitor activity. N Engl J Med. 2015;17(373):2413–24.CrossRef Siegal DM, Curnutte JT, Connolly SJ, et al. Andexanet alfa for the reversal of factor Xa inhibitor activity. N Engl J Med. 2015;17(373):2413–24.CrossRef
27.
Zurück zum Zitat Pernod G, Albaladejo P, Godier A, et al. Management of major bleeding complications and emergency surgery in patients on long-term treatment with direct oral anticoagulants, thrombin or factor-Xa inhibitors: proposals of the Working Group on Perioperative Haemostasis (GIHP). Ann Fr Anesth Reanim. 2013;32:691–700.CrossRefPubMed Pernod G, Albaladejo P, Godier A, et al. Management of major bleeding complications and emergency surgery in patients on long-term treatment with direct oral anticoagulants, thrombin or factor-Xa inhibitors: proposals of the Working Group on Perioperative Haemostasis (GIHP). Ann Fr Anesth Reanim. 2013;32:691–700.CrossRefPubMed
28.
Zurück zum Zitat Moll J, Kerns W, Tomaszewski C, Rose R. Incidence of aspiration pneumonia in intubated patients receiving activated charcoal. J Emerg Med. 1999;17:279–83.CrossRefPubMed Moll J, Kerns W, Tomaszewski C, Rose R. Incidence of aspiration pneumonia in intubated patients receiving activated charcoal. J Emerg Med. 1999;17:279–83.CrossRefPubMed
Metadaten
Titel
Effect of Activated Charcoal on Rivaroxaban Complex Absorption
verfasst von
Edouard Ollier
Sophie Hodin
Julien Lanoiselée
Jean Escal
Sandrine Accassat
Elodie De Magalhaes
Thierry Basset
Laurent Bertoletti
Patrick Mismetti
Xavier Delavenne
Publikationsdatum
02.12.2016
Verlag
Springer International Publishing
Erschienen in
Clinical Pharmacokinetics / Ausgabe 7/2017
Print ISSN: 0312-5963
Elektronische ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-016-0485-1

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