Effect of Activated Charcoal on Rivaroxaban Complex Absorption

被引:35
作者
Ollier, Edouard [1 ,2 ,5 ]
Hodin, Sophie [2 ]
Lanoiselee, Julien [1 ,2 ]
Escal, Jean [1 ,2 ]
Accassat, Sandrine [2 ,4 ,6 ]
De Magalhaes, Elodie [1 ,3 ]
Basset, Thierry [1 ,2 ]
Bertoletti, Laurent [1 ,3 ,4 ]
Mismetti, Patrick [1 ,3 ,4 ]
Delavenne, Xavier [1 ,2 ,4 ]
机构
[1] INSERM, U1059, Dysfonct Vasc & Hemostase, St Etienne, France
[2] Hop Nord St Etienne, CHU St Etienne, INSERM UMR 1059, Lab Pharmacol Toxicol, F-42055 St Etienne, France
[3] CHU St Etienne, Serv Med Therapeut, St Etienne, France
[4] Univ Lyon, Univ Jean Monnet, St Etienne, France
[5] Univ Claude Bernard Lyon 1, Villeurbanne, France
[6] CHU St Etienne, Unite Rech Clin Innovat & Pharmacol, St Etienne, France
关键词
FACTOR-XA INHIBITOR; ORAL ANTICOAGULANTS; PHARMACOKINETICS; MODEL; PHARMACODYNAMICS; DABIGATRAN; APIXABAN; OVERDOSE; DRUGS; FOOD;
D O I
10.1007/s40262-016-0485-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:793 / 801
页数:9
相关论文
共 28 条
  • [1] The pharmacokinetics of sertraline in overdose and the effect of activated charcoal
    Cooper, Joyce M.
    Duffull, Stephen B.
    Saiao, Ana S.
    Isbister, Geoffrey K.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 79 (02) : 307 - 315
  • [2] The use of a sum of inverse Gaussian functions to describe the absorption profile of drugs exhibiting complex absorption
    Csajka, C
    Drover, D
    Verotta, D
    [J]. PHARMACEUTICAL RESEARCH, 2005, 22 (08) : 1227 - 1235
  • [3] European Medicines Agency, 2008, CHMP XAR INN RIV
  • [4] Holford N., 2005, VISUAL PREDICTIVE CH
  • [5] Activated charcoal for acute overdose: a reappraisal
    Juurlink, David N.
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2016, 81 (03) : 482 - 487
  • [6] Kuhn E., 2004, ESAIM Probab. Stat, V8, P115, DOI [DOI 10.1051/PS:2004007, 10.1051/ps:2004007]
  • [7] What do we mean by identifiability in mixed effects models?
    Lavielle, Marc
    Aarons, Leon
    [J]. JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2016, 43 (01) : 111 - 122
  • [8] Incidence of aspiration pneumonia in intubated patients receiving activated charcoal
    Moll, J
    Kerns, W
    Tomaszewski, C
    Rose, R
    [J]. JOURNAL OF EMERGENCY MEDICINE, 1999, 17 (02) : 279 - 283
  • [9] Mueck W, 2007, INT J CLIN PHARM TH, V45, P335
  • [10] Population pharmacokinetics and pharmacodynamics of once- and twice-daily rivaroxaban for the prevention of venous thromboembolism in patients undergoing total hip replacement
    Mueck, Wolfgang
    Borris, Lars C.
    Dahl, Ola E.
    Haas, Sylvia
    Huisman, MennoV.
    Kakkar, Ajay K.
    Kalebo, Peter
    Muelhofer, Eva
    Misselwitz, Frank
    Eriksson, Bengt I.
    [J]. THROMBOSIS AND HAEMOSTASIS, 2008, 100 (03) : 453 - 461