Document Type

Journal Article

Department/Unit

Department of Chemistry

Title

Application of static modeling ­­in the prediction of in vivo drug–drug interactions between rivaroxaban and antiarrhythmic agents based on in vitro inhibition studies

Language

English

Abstract

Rivaroxaban, a direct Factor Xa inhibitor, is indicated for stroke prevention in nonvalvular atrial fibrillation (AF). Studies have revealed that the clearance of rivaroxaban is largely attributed to CYP3A4, CYP2J2 metabolism, and P-glycoprotein (P-gp) efflux pathways. Amiodarone and dronedarone are antiarrhythmic agents employed in AF management. Amiodarone, dronedarone, and their major metabolites, N-desethylamiodarone (NDEA) and N-desbutyldronedarone (NDBD), demonstrate inhibitory effects on CYP3A4 and CYP2J2 with U.S. Food and Drug Administration–recommended probe substrates. In addition, both amiodarone and dronedarone are known P-gp inhibitors. Hence, the concomitant administration of these antiarrhythmic agents has the potential to augment the systemic exposure of rivaroxaban through simultaneous impairment of its clearance pathways. Currently, however, clinical data on the extent of these postulated drug–drug interactions are lacking. In this study, in vitro inhibition assays using rivaroxaban as the probe substrate demonstrated that both dronedarone and NDBD produced reversible inhibition as well as irreversible mechanism-based inactivation of CYP3A4- and CYP2J2-mediated metabolism of rivaroxaban. However, amiodarone and NDEA were observed to cause reversible inhibition as well as mechanism-based inactivation of CYP3A4 but not CYP2J2. In addition, amiodarone, NDEA, and dronedarone, but not NDBD, were determined to inhibit P-gp–mediated rivaroxaban transport. The in vitro inhibition parameters were fitted into a mechanistic static model, which predicted a 37% and 31% increase in rivaroxaban exposure due to the inhibition of hepatic and gut metabolism by amiodarone and dronedarone, respectively. A separate model quantifying the inhibition of P-gp–mediated efflux by amiodarone or dronedarone projected a 9% increase in rivaroxaban exposure.

Keywords

Rivaroxaban, Amiodarone, Dronedarone, CYP3A4, CYP2J2, P-glycoprotein, Static modeling

Publication Date

3-2017

Source Publication Title

Drug Metabolism and Disposition

Volume

45

Issue

3

Start Page

260

End Page

268

Publisher

American Society for Pharmacology and Experimental Therapeutics (ASPET)

Peer Reviewed

1

Funder

This work was supported by the Singapore Ministry of Education Tier 1 Academic Research Funding [Grant R-148-000-193-112] and the National University of Singapore, Department of Pharmacy, Final Year Project Funding [Grant C-148-000-003-001] provided to Eric Chun Yong Chan.

DOI

10.1124/dmd.116.073890

Link to Publisher's Edition

http://dx.doi.org/10.1124/dmd.116.073890

ISSN (print)

00909556

ISSN (electronic)

1521009X

This document is currently not available here.

Share

COinS