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Volumn 45, Issue 7, 2017, Pages 755-764

Mechanisms and predictions of drug-drug interactions of the hepatitis C virus three direct-acting antiviral regimen: Paritaprevir/ritonavir, ombitasvir, and dasabuvir

Author keywords

[No Author keywords available]

Indexed keywords

BREAST CANCER RESISTANCE PROTEIN; CYTOCHROME P450 2C8; CYTOCHROME P450 3A; DASABUVIR; DRUG METABOLIZING ENZYME; GLUCURONOSYLTRANSFERASE; OMBITASVIR; PARITAPREVIR; RITONAVIR; SOLUTE CARRIER ORGANIC ANION TRANSPORTER 1B1; SOLUTE CARRIER ORGANIC ANION TRANSPORTER 1B3; ABT-267; ABT-333; ABT-450; ANILIDE; ANTIVIRUS AGENT; CARBAMIC ACID DERIVATIVE; CARRIER PROTEIN; CYTOCHROME P450; CYTOCHROME P450 INHIBITOR; MACROCYCLIC COMPOUND; MULTIDRUG RESISTANCE PROTEIN 1; SULFONAMIDE; URACIL;

EID: 85020907428     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.116.074518     Document Type: Article
Times cited : (36)

References (33)
  • 1
    • 84928068548 scopus 로고    scopus 로고
    • Pharmacokinetics and dose recommendations for cyclosporine and tacrolimus when coadministered with ABT-450, ombitasvir, and dasabuvir
    • Badri P, Dutta S, Coakley E, Cohen D, Ding B, Podsadecki T, Bernstein B, Awni W, and Menon R (2015) Pharmacokinetics and dose recommendations for cyclosporine and tacrolimus when coadministered with ABT-450, ombitasvir, and dasabuvir. Am J Transplant 15: 1313–1322.
    • (2015) Am J Transplant , vol.15 , pp. 1313-1322
    • Badri, P.1    Dutta, S.2    Coakley, E.3    Cohen, D.4    Ding, B.5    Podsadecki, T.6    Bernstein, B.7    Awni, W.8    Menon, R.9
  • 2
    • 27444445468 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
    • Brown HS, Ito K, Galetin A, and Houston JB (2005) Prediction of in vivo drug-drug interactions from in vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 60: 508–518.
    • (2005) Br J Clin Pharmacol , vol.60 , pp. 508-518
    • Brown, H.S.1    Ito, K.2    Galetin, A.3    Houston, J.B.4
  • 4
    • 84893565092 scopus 로고    scopus 로고
    • In vitro oatp1b1 and oatp1b3 inhibition is associated with observations of benign clinical unconjugated hyperbilirubinemia
    • Chiou WJ, de Morais SM, Kikuchi R, Voorman RL, Li X, and Bow DA (2014) In vitro OATP1B1 and OATP1B3 inhibition is associated with observations of benign clinical unconjugated hyperbilirubinemia. Xenobiotica 44: 276–282.
    • (2014) Xenobiotica , vol.44 , pp. 276-282
    • Chiou, W.J.1    De Morais, S.M.2    Kikuchi, R.3    Voorman, R.L.4    Li, X.5    Bow, D.A.6
  • 5
    • 77954371490 scopus 로고    scopus 로고
    • Hepatic OATP and OCT uptake transporters: Their role for drug-drug interactions and pharmacogenetic aspects
    • Fahrmayr C, Fromm MF, and König J (2010) Hepatic OATP and OCT uptake transporters: their role for drug-drug interactions and pharmacogenetic aspects. Drug Metab Rev 42: 380–401.
    • (2010) Drug Metab Rev , vol.42 , pp. 380-401
    • Fahrmayr, C.1    Fromm, M.F.2    König, J.3
  • 8
    • 84896388709 scopus 로고    scopus 로고
    • Establishment of optimized mdck cell lines for reliable efflux transport studies
    • Gartzke D and Fricker G (2014) Establishment of optimized MDCK cell lines for reliable efflux transport studies. J Pharm Sci 103: 1298–1304.
    • (2014) J Pharm Sci , vol.103 , pp. 1298-1304
    • Gartzke, D.1    Fricker, G.2
  • 9
    • 84880271700 scopus 로고    scopus 로고
    • Mechanisms of pharmacokinetic enhancement between ritonavir and saquinavir; micro/small dosing tests using midazolam (CYP3A4), fexofenadine (p-glycoprotein), and pravastatin (OATP1B1) as probe drugs
    • Ieiri I, Tsunemitsu S, Maeda K, Ando Y, Izumi N, Kimura M, Yamane N, Okuzono T, Morishita M, Kotani N, et al. (2013) Mechanisms of pharmacokinetic enhancement between ritonavir and saquinavir; micro/small dosing tests using midazolam (CYP3A4), fexofenadine (p-glycoprotein), and pravastatin (OATP1B1) as probe drugs. J Clin Pharmacol 53: 654–661.
    • (2013) J Clin Pharmacol , vol.53 , pp. 654-661
    • Ieiri, I.1    Tsunemitsu, S.2    Maeda, K.3    Ando, Y.4    Izumi, N.5    Kimura, M.6    Yamane, N.7    Okuzono, T.8    Morishita, M.9    Kotani, N.10
  • 10
    • 84891867228 scopus 로고    scopus 로고
    • A mechanistic framework for in vitro-in vivo extrapolation of liver membrane transporters: Prediction of drug-drug interaction between rosuvastatin and cyclosporine
    • Jamei M, Bajot F, Neuhoff S, Barter Z, Yang J, Rostami-Hodjegan A, and Rowland-Yeo K (2014) A mechanistic framework for in vitro-in vivo extrapolation of liver membrane transporters: prediction of drug-drug interaction between rosuvastatin and cyclosporine. Clin Pharmacokinet 53: 73–87.
    • (2014) Clin Pharmacokinet , vol.53 , pp. 73-87
    • Jamei, M.1    Bajot, F.2    Neuhoff, S.3    Barter, Z.4    Yang, J.5    Rostami-Hodjegan, A.6    Rowland-Yeo, K.7
  • 11
    • 84930085341 scopus 로고    scopus 로고
    • Clinical pharmacology profile of boceprevir, a hepatitis C virus NS3 protease inhibitor: focus on drug-drug interactions
    • Khalilieh S, Feng HP, Hulskotte EG, Wenning LA, and Butterton JR (2015) Clinical pharmacology profile of boceprevir, a hepatitis C virus NS3 protease inhibitor: focus on drug-drug interactions. Clin Pharmacokinet 54: 599–614.
    • (2015) Clin Pharmacokinet , vol.54 , pp. 599-614
    • Khalilieh, S.1    Feng, H.P.2    Hulskotte, E.G.3    Wenning, L.A.4    Butterton, J.R.5
  • 12
    • 84964825681 scopus 로고    scopus 로고
    • Evaluation of drug-drug interactions between hepatitis C antiviral agents ombitasvir, paritaprevir/ritonavir, and dasabuvir and HIV-1 protease inhibitors
    • Khatri A, Dutta S, Wang H, Podsadecki T, Trinh R, Awni W, and Menon R (2016) Evaluation of drug-drug interactions between hepatitis C antiviral agents ombitasvir, paritaprevir/ritonavir, and dasabuvir and HIV-1 protease inhibitors. Clin Infect Dis 62: 972–979.
    • (2016) Clin Infect Dis , vol.62 , pp. 972-979
    • Khatri, A.1    Dutta, S.2    Wang, H.3    Podsadecki, T.4    Trinh, R.5    Awni, W.6    Menon, R.7
  • 13
    • 84888205222 scopus 로고    scopus 로고
    • Prediction of clinical drug-drug interactions of veliparib (ABT-888) with human renal transporters (OAT1, OAT3, OCT2, MATE1, and MATE2K)
    • Kikuchi R, Lao Y, Bow DA, Chiou WJ, Andracki ME, Carr RA, Voorman RL, and De Morais SM (2013) Prediction of clinical drug-drug interactions of veliparib (ABT-888) with human renal transporters (OAT1, OAT3, OCT2, MATE1, and MATE2K). J Pharm Sci 102: 4426–4432.
    • (2013) J Pharm Sci , vol.102 , pp. 4426-4432
    • Kikuchi, R.1    Lao, Y.2    Bow, D.A.3    Chiou, W.J.4    Andracki, M.E.5    Carr, R.A.6    Voorman, R.L.7    De Morais, S.M.8
  • 14
    • 84933671704 scopus 로고    scopus 로고
    • Pharmacokinetic, pharmacody-namic, and drug-interaction profile of the hepatitis C virus NS5B polymerase inhibitor sofosbuvir
    • Kirby BJ, Symonds WT, Kearney BP, and Mathias AA (2015) Pharmacokinetic, pharmacody-namic, and drug-interaction profile of the hepatitis C virus NS5B polymerase inhibitor sofosbuvir. Clin Pharmacokinet 54: 677–690.
    • (2015) Clin Pharmacokinet , vol.54 , pp. 677-690
    • Kirby, B.J.1    Symonds, W.T.2    Kearney, B.P.3    Mathias, A.A.4
  • 15
    • 0030430035 scopus 로고    scopus 로고
    • Cytochrome P450-mediated metabolism of the HIV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes
    • Kumar GN, Rodrigues AD, Buko AM, and Denissen JF (1996) Cytochrome P450-mediated metabolism of the HIV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes. J Pharmacol Exp Ther 277: 423–431.
    • (1996) J Pharmacol Exp Ther , vol.277 , pp. 423-431
    • Kumar, G.N.1    Rodrigues, A.D.2    Buko, A.M.3    Denissen, J.F.4
  • 19
    • 84952984602 scopus 로고    scopus 로고
    • Population pharmacokinetics of paritaprevir, ombitasvir, dasabuvir, ritonavir, and ribavirin in patients with hepatitis c virus genotype 1 infection: Combined analysis from 9 phase 1b/2 studies
    • Mensing S, Polepally AR, König D, Khatri A, Liu W, Podsadecki TJ, Awni WM, Menon RM, and Dutta S (2016) Population pharmacokinetics of paritaprevir, ombitasvir, dasabuvir, ritonavir, and ribavirin in patients with hepatitis C virus genotype 1 infection: combined analysis from 9 phase 1b/2 studies. AAPS J 18: 270–280.
    • (2016) AAPS J , vol.18 , pp. 270-280
    • Mensing, S.1    Polepally, A.R.2    König, D.3    Khatri, A.4    Liu, W.5    Podsadecki, T.J.6    Awni, W.M.7    Menon, R.M.8    Dutta, S.9
  • 20
    • 84893258687 scopus 로고    scopus 로고
    • Suitability of digoxin as a p-glycoprotein probe: Implications of other transporters on sensitivity and specificity
    • Nader AM and Foster DR (2014) Suitability of digoxin as a P-glycoprotein probe: implications of other transporters on sensitivity and specificity. J Clin Pharmacol 54: 3–13.
    • (2014) J Clin Pharmacol , vol.54 , pp. 3-13
    • Nader, A.M.1    Foster, D.R.2
  • 21
    • 84881609366 scopus 로고    scopus 로고
    • Application of permeability-limited physiologically-based pharmacokinetic models: Part II - prediction of p-glycoprotein mediated drug-drug interactions with digoxin
    • Neuhoff S, Yeo KR, Barter Z, Jamei M, Turner DB, and Rostami-Hodjegan A (2013) Application of permeability-limited physiologically-based pharmacokinetic models: part II - prediction of P-glycoprotein mediated drug-drug interactions with digoxin. J Pharm Sci 102: 3161–3173.
    • (2013) J Pharm Sci , vol.102 , pp. 3161-3173
    • Neuhoff, S.1    Yeo, K.R.2    Barter, Z.3    Jamei, M.4    Turner, D.B.5    Rostami-Hodjegan, A.6
  • 22
    • 84983080825 scopus 로고    scopus 로고
    • Drug-drug interactions between the anti-hepatitis c virus 3d regimen of ombitasvir, paritaprevir/ritonavir, and dasabuvir and eight commonly used medications in healthy volunteers
    • Polepally AR, King JR, Ding B, Shuster DL, Dumas EO, Khatri A, Chiu YL, Podsadecki TJ, and Menon RM (2016) Drug-drug interactions between the anti-hepatitis C virus 3D regimen of ombitasvir, paritaprevir/ritonavir, and dasabuvir and eight commonly used medications in healthy volunteers. Clin Pharmacokinet 55: 1003–1014.
    • (2016) Clin Pharmacokinet , vol.55 , pp. 1003-1014
    • Polepally, A.R.1    King, J.R.2    Ding, B.3    Shuster, D.L.4    Dumas, E.O.5    Khatri, A.6    Chiu, Y.L.7    Podsadecki, T.J.8    Menon, R.M.9
  • 23
    • 77549084821 scopus 로고    scopus 로고
    • Physiologically based mechanistic modelling to predict complex drug-drug interactions involving simultaneous competitive and time-dependent enzyme inhibition by parent compound and its metabolite in both liver and gut - the effect of diltiazem on the time-course of exposure to triazolam
    • Rowland Yeo K, Jamei M, Yang J, Tucker GT, and Rostami-Hodjegan A (2010) Physiologically based mechanistic modelling to predict complex drug-drug interactions involving simultaneous competitive and time-dependent enzyme inhibition by parent compound and its metabolite in both liver and gut - the effect of diltiazem on the time-course of exposure to triazolam. Eur J Pharm Sci 39: 298–309.
    • (2010) Eur J Pharm Sci , vol.39 , pp. 298-309
    • Rowland Yeo, K.1    Jamei, M.2    Yang, J.3    Tucker, G.T.4    Rostami-Hodjegan, A.5
  • 26
    • 78650808366 scopus 로고    scopus 로고
    • The relevance of assessment of intestinal p-gp inhibition using digoxin as an in vivo probe substrate
    • author reply 75
    • Shi JG, Zhang Y, and Yeleswaram S (2011) The relevance of assessment of intestinal P-gp inhibition using digoxin as an in vivo probe substrate. Nat Rev Drug Discov 10: 75–, author reply 75.
    • (2011) Nat Rev Drug Discov , vol.10 , pp. 75
    • Shi, J.G.1    Zhang, Y.2    Yeleswaram, S.3
  • 29
    • 84866708911 scopus 로고    scopus 로고
    • Physiologically based modeling of pravastatin transporter-mediated hepatobiliary disposition and drug-drug interactions
    • Varma MV, Lai Y, Feng B, Litchfield J, Goosen TC, and Bergman A (2012) Physiologically based modeling of pravastatin transporter-mediated hepatobiliary disposition and drug-drug interactions. Pharm Res 29: 2860–2873.
    • (2012) Pharm Res , vol.29 , pp. 2860-2873
    • Varma, M.V.1    Lai, Y.2    Feng, B.3    Litchfield, J.4    Goosen, T.C.5    Bergman, A.6
  • 31
    • 80053923193 scopus 로고    scopus 로고
    • Hepatitis C
    • World Health Organization
    • World Health Organization (2011) Hepatitis C. Wkly Epidemiol Rec 86: 445–447.
    • (2011) Wkly Epidemiol Rec , vol.86 , pp. 445-447
  • 32
    • 33745433348 scopus 로고    scopus 로고
    • Lopinavir/ritonavir induces the hepatic activity of cytochrome p450 enzymes cyp2c9, cyp2c19, and cyp1a2 but inhibits the hepatic and intestinal activity of cyp3a as measured by a phenotyping drug cocktail in healthy volunteers
    • Yeh RF, Gaver VE, Patterson KB, Rezk NL, Baxter-Meheux F, Blake MJ, Eron JJ, Jr, Klein CE, Rublein JC, and Kashuba AD (2006) Lopinavir/ritonavir induces the hepatic activity of cytochrome P450 enzymes CYP2C9, CYP2C19, and CYP1A2 but inhibits the hepatic and intestinal activity of CYP3A as measured by a phenotyping drug cocktail in healthy volunteers. J Acquir Immune Defic Syndr 42: 52–60.
    • (2006) J Acquir Immune Defic Syndr , vol.42 , pp. 52-60
    • Yeh, R.F.1    Gaver, V.E.2    Patterson, K.B.3    Rezk, N.L.4    Baxter-Meheux, F.5    Blake, M.J.6    Eron, J.J.7    Klein, C.E.8    Rublein, J.C.9    Kashuba, A.D.10
  • 33
    • 79251474385 scopus 로고    scopus 로고
    • Correlation between bilirubin glucuronidation and estradiol-3-gluronidation in the presence of model udp-glucuronosyltransferase 1a1 substrates/inhibitors
    • Zhou J, Tracy TS, and Remmel RP (2011) Correlation between bilirubin glucuronidation and estradiol-3-gluronidation in the presence of model UDP-glucuronosyltransferase 1A1 substrates/inhibitors. Drug Metab Dispos 39: 322–329.
    • (2011) Drug Metab Dispos , vol.39 , pp. 322-329
    • Zhou, J.1    Tracy, T.S.2    Remmel, R.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.