메뉴 건너뛰기




Volumn 33, Issue 6, 2005, Pages 726-732

Nonlinear pharmacokinetics of propafenone in rats and humans: Application of a substrate depletion assay using hepatocytes for assessment of nonlinearity

Author keywords

[No Author keywords available]

Indexed keywords

HUMAN SERUM ALBUMIN; OROSOMUCOID; PROPAFENONE;

EID: 18844363220     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: 10.1124/dmd.104.002550     Document Type: Article
Times cited : (19)

References (34)
  • 1
    • 0842332512 scopus 로고    scopus 로고
    • High-throughput screening for stability and inhibitory activity of compounds toward cytochrome P450-mediated metabolism
    • Ansede JH and Thakker DR (2004) High-throughput screening for stability and inhibitory activity of compounds toward cytochrome P450-mediated metabolism. J Pharm Sci 93:239-255.
    • (2004) J Pharm Sci , vol.93 , pp. 239-255
    • Ansede, J.H.1    Thakker, D.R.2
  • 2
    • 0025185309 scopus 로고
    • Dose-dependent kinetics of methylphenidate enantiomers after oral administration of racemic methylphenidate to rats
    • Aoyama T, Kotaki H, and Iga T (1990) Dose-dependent kinetics of methylphenidate enantiomers after oral administration of racemic methylphenidate to rats. J Pharmacobio-Dyn 13:647-652.
    • (1990) J Pharmacobio-Dyn , vol.13 , pp. 647-652
    • Aoyama, T.1    Kotaki, H.2    Iga, T.3
  • 3
    • 0027460033 scopus 로고
    • Identification and characterization of the cytochrome P450 enzymes involved in N-dealkylation of propafenone: Molecular base for interaction potential and variable disposition of active metabolites
    • Botsch S, Gautier J-C, Beaune P, Eichelbaum M, and Kroemer HK (1993) Identification and characterization of the cytochrome P450 enzymes involved in N-dealkylation of propafenone: molecular base for interaction potential and variable disposition of active metabolites. Mol Pharmacol 43:120-126.
    • (1993) Mol Pharmacol , vol.43 , pp. 120-126
    • Botsch, S.1    Gautier, J.-C.2    Beaune, P.3    Eichelbaum, M.4    Kroemer, H.K.5
  • 4
    • 0018967595 scopus 로고
    • Interspecies variation in liver weight, hepatic blood flow and antipyrine intrinsic clearance: Extrapolation of data to benzodiazepines and phenytoin
    • Boxenbaum H (1980) Interspecies variation in liver weight, hepatic blood flow and antipyrine intrinsic clearance: extrapolation of data to benzodiazepines and phenytoin. J Pharmacokinet Biopharm 8:165-176.
    • (1980) J Pharmacokinet Biopharm , vol.8 , pp. 165-176
    • Boxenbaum, H.1
  • 5
    • 0034824439 scopus 로고    scopus 로고
    • Utility of metabolic stability screening: Comparison of in vitro and in vivo clearance
    • Clarke SE and Jeffrey P (2001) Utility of metabolic stability screening: comparison of in vitro and in vivo clearance. Xenobiotica 31:591-598.
    • (2001) Xenobiotica , vol.31 , pp. 591-598
    • Clarke, S.E.1    Jeffrey, P.2
  • 6
    • 0025171473 scopus 로고
    • The relationship between the pharmacokinetics of ibuprofen enantiomers and the dose of racemic ibuprofen in humans
    • Evans AM, Nation RL, Sansom LN, Bochner F, and Somogyi AA (1990) The relationship between the pharmacokinetics of ibuprofen enantiomers and the dose of racemic ibuprofen in humans. Biopharm Drug Dispos 11:507-518.
    • (1990) Biopharm Drug Dispos , vol.11 , pp. 507-518
    • Evans, A.M.1    Nation, R.L.2    Sansom, L.N.3    Bochner, F.4    Somogyi, A.A.5
  • 8
    • 2042504362 scopus 로고    scopus 로고
    • Comparison of fresh and cryopreserved rat hepatocyte suspensions for the prediction of in vitro intrinsic clearance
    • Griffin SJ and Houston JB (2004) Comparison of fresh and cryopreserved rat hepatocyte suspensions for the prediction of in vitro intrinsic clearance. Drug Metab Dispos 32:552-558.
    • (2004) Drug Metab Dispos , vol.32 , pp. 552-558
    • Griffin, S.J.1    Houston, J.B.2
  • 9
    • 0032859194 scopus 로고    scopus 로고
    • Nonlinear disposition kinetics of a novel antifolate, MX-68, in rats
    • Han YH, Kato Y, and Sugiyama Y (1999) Nonlinear disposition kinetics of a novel antifolate, MX-68, in rats. J Pharmacol Exp Ther 291:204-212.
    • (1999) J Pharmacol Exp Ther , vol.291 , pp. 204-212
    • Han, Y.H.1    Kato, Y.2    Sugiyama, Y.3
  • 10
    • 0034899540 scopus 로고    scopus 로고
    • ADMET - Turning chemicals into drugs
    • Hodgson J (2001) ADMET - turning chemicals into drugs. Nat Biotechnol 19:722-726.
    • (2001) Nat Biotechnol , vol.19 , pp. 722-726
    • Hodgson, J.1
  • 12
    • 0034105896 scopus 로고    scopus 로고
    • In vitro-in vivo scaling of CYP kinetic data not consistent with classical Michaelis-Menten model
    • Houston JB and Kenworthy KE (2000) In vitro-in vivo scaling of CYP kinetic data not consistent with classical Michaelis-Menten model. Drug Metab Dispos 28:246-254.
    • (2000) Drug Metab Dispos , vol.28 , pp. 246-254
    • Houston, J.B.1    Kenworthy, K.E.2
  • 13
    • 0034894719 scopus 로고    scopus 로고
    • Human alpha-1-glycoprotein and its interactions with drugs
    • Israili ZH and Dayton PG (2001) Human alpha-1-glycoprotein and its interactions with drugs. Drug Metab Rev 33:161-235.
    • (2001) Drug Metab Rev , vol.33 , pp. 161-235
    • Israili, Z.H.1    Dayton, P.G.2
  • 14
    • 0029950964 scopus 로고    scopus 로고
    • Prediction of in vivo drug disposition from in vitro data based on physiological pharmacokinetics
    • Iwatsubo T, Hirota N, Ooie T, Suzuki H, and Sugiyama Y (1996) Prediction of in vivo drug disposition from in vitro data based on physiological pharmacokinetics. Biopharm Drug Dispos 17:273-310.
    • (1996) Biopharm Drug Dispos , vol.17 , pp. 273-310
    • Iwatsubo, T.1    Hirota, N.2    Ooie, T.3    Suzuki, H.4    Sugiyama, Y.5
  • 15
    • 0031870866 scopus 로고    scopus 로고
    • Prediction of in vivo nonlinear first-pass hepatic metabolism of YM796 from in vitro metabolic data
    • Iwatsubo T, Hisaka A, Suzuki H, and Sugiyama Y (1998) Prediction of in vivo nonlinear first-pass hepatic metabolism of YM796 from in vitro metabolic data. J Pharmacol Exp Ther 286:122-127.
    • (1998) J Pharmacol Exp Ther , vol.286 , pp. 122-127
    • Iwatsubo, T.1    Hisaka, A.2    Suzuki, H.3    Sugiyama, Y.4
  • 16
    • 0036761676 scopus 로고    scopus 로고
    • Improvement of "hit-to-lead" optimization by integration of in vitro HTS experimental models for early determination of pharmacokinetic properties
    • Kariv I, Rourick RA, Kassel DB, and Chung TD (2002) Improvement of "hit-to-lead" optimization by integration of in vitro HTS experimental models for early determination of pharmacokinetic properties. Comb Chem High Throughput Screen 5:459-472.
    • (2002) Comb Chem High Throughput Screen , vol.5 , pp. 459-472
    • Kariv, I.1    Rourick, R.A.2    Kassel, D.B.3    Chung, T.D.4
  • 17
    • 0030763543 scopus 로고    scopus 로고
    • Drug metabolism in hepatocyte sandwich cultures of rats and humans
    • Kern A, Bader A, Pichlmayr R, and Sewing KF (1997) Drug metabolism in hepatocyte sandwich cultures of rats and humans. Biochem Pharmacol 54:761-772.
    • (1997) Biochem Pharmacol , vol.54 , pp. 761-772
    • Kern, A.1    Bader, A.2    Pichlmayr, R.3    Sewing, K.F.4
  • 18
    • 0032864188 scopus 로고    scopus 로고
    • Physiological based pharmacokinetics of KNI-272, a tripeptide HIV-1 protease inhibitor
    • Kiriyama A, Nishiura T, Yamaji H, and Takada K (1999) Physiological based pharmacokinetics of KNI-272, a tripeptide HIV-1 protease inhibitor. Biopharm Drug Dispos 20:199-205.
    • (1999) Biopharm Drug Dispos , vol.20 , pp. 199-205
    • Kiriyama, A.1    Nishiura, T.2    Yamaji, H.3    Takada, K.4
  • 20
    • 14344255557 scopus 로고    scopus 로고
    • Pharmacokinetics and metabolism of metoprolol and propranolol in the female DA and female Wistar rat: The female DA rat is not always an animal model for poor metabolizers of CYP2D6
    • Komura H and Iwaki M (2005) Pharmacokinetics and metabolism of metoprolol and propranolol in the female DA and female Wistar rat: the female DA rat is not always an animal model for poor metabolizers of CYP2D6. J Pharm Sci 94:397-408.
    • (2005) J Pharm Sci , vol.94 , pp. 397-408
    • Komura, H.1    Iwaki, M.2
  • 21
    • 0025823440 scopus 로고
    • Enantiomer/enantiomer interaction of (S)- And (R)-propafenone for cytochrome P450IID6-catalyzed 5-hydroxylation: In vitro evaluation of the mechanism
    • Kroemer HK, Fischer C, Meese CO, and Eichelbaum M (1991) Enantiomer/enantiomer interaction of (S)- and (R)-propafenone for cytochrome P450IID6-catalyzed 5-hydroxylation: in vitro evaluation of the mechanism. Mol Pharmacol 40:135-142.
    • (1991) Mol Pharmacol , vol.40 , pp. 135-142
    • Kroemer, H.K.1    Fischer, C.2    Meese, C.O.3    Eichelbaum, M.4
  • 22
    • 0024548251 scopus 로고
    • In vitro characterization of the human cytochrome P-450 involved in polymorphic oxidation of propafenone
    • Kroemer HK, Mikus G, Kronbach T, Myer UA, and Eicheilbaum M (1989) In vitro characterization of the human cytochrome P-450 involved in polymorphic oxidation of propafenone. Clin Pharmacol Ther 45:28-33.
    • (1989) Clin Pharmacol Ther , vol.45 , pp. 28-33
    • Kroemer, H.K.1    Mikus, G.2    Kronbach, T.3    Myer, U.A.4    Eicheilbaum, M.5
  • 23
    • 0036893242 scopus 로고    scopus 로고
    • Development of a novel in vitro model to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes
    • Lau YY, Sapidou E, Cui X, White RE, and Cheng K-C (2002) Development of a novel in vitro model to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes. Drug Metab Dispos 30:1446-1454.
    • (2002) Drug Metab Dispos , vol.30 , pp. 1446-1454
    • Lau, Y.Y.1    Sapidou, E.2    Cui, X.3    White, R.E.4    Cheng, K.-C.5
  • 24
    • 0025854599 scopus 로고
    • Nonlinear pharamacokinetics: Clinical implications
    • Ludden TM (1991) Nonlinear pharamacokinetics: clinical implications. Clin Pharmacokinet 20:429-446.
    • (1991) Clin Pharmacokinet , vol.20 , pp. 429-446
    • Ludden, T.M.1
  • 25
    • 0037403950 scopus 로고    scopus 로고
    • Utility of hepatocytes in predicting drug metabolism: Comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro
    • Naritomi Y, Terashita S, Kagayama A, and Sugiyama Y (2003) Utility of hepatocytes in predicting drug metabolism: comparison of hepatic intrinsic clearance in rats and humans in vivo and in vitro. Drug Metab Dispos 31:580-588.
    • (2003) Drug Metab Dispos , vol.31 , pp. 580-588
    • Naritomi, Y.1    Terashita, S.2    Kagayama, A.3    Sugiyama, Y.4
  • 26
    • 8944252342 scopus 로고    scopus 로고
    • Dose dependent pharmacokinetics of naproxen in man
    • Niazi SK, Alam SM, and Ahmad SI (1996) Dose dependent pharmacokinetics of naproxen in man. Biopharm Drug Dispos 17:355-361.
    • (1996) Biopharm Drug Dispos , vol.17 , pp. 355-361
    • Niazi, S.K.1    Alam, S.M.2    Ahmad, S.I.3
  • 27
    • 0035987898 scopus 로고    scopus 로고
    • Measurement of Michaelis constants for cytochrome P450-mediated biotransformation reactions using a substrate depletion approach
    • Obach RS and Reed-Hagen AE (2002) Measurement of Michaelis constants for cytochrome P450-mediated biotransformation reactions using a substrate depletion approach. Drug Metab Dispos 30:831-837.
    • (2002) Drug Metab Dispos , vol.30 , pp. 831-837
    • Obach, R.S.1    Reed-Hagen, A.E.2
  • 28
    • 0017603437 scopus 로고
    • Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred" model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding and the hepatocellular enzymatic activity on hepatic drug clearance
    • Pang KS and Rowland M (1977) Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred" model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding and the hepatocellular enzymatic activity on hepatic drug clearance. J Pharmacokinet Biopharm 5:625-653.
    • (1977) J Pharmacokinet Biopharm , vol.5 , pp. 625-653
    • Pang, K.S.1    Rowland, M.2
  • 29
    • 0034837087 scopus 로고    scopus 로고
    • High-throughput screening approaches for investigating drug metabolism and pharmacokinetics
    • Roberts SA (2001) High-throughput screening approaches for investigating drug metabolism and pharmacokinetics. Xenobiotica 31:557-589.
    • (2001) Xenobiotica , vol.31 , pp. 557-589
    • Roberts, S.A.1
  • 30
    • 0036320379 scopus 로고    scopus 로고
    • Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: An application of serum incubation method
    • Shibata Y, Takahashi H, Chiba M, and Ishii Y (2002) Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: an application of serum incubation method. Drug Metab Dispos 30:892-896.
    • (2002) Drug Metab Dispos , vol.30 , pp. 892-896
    • Shibata, Y.1    Takahashi, H.2    Chiba, M.3    Ishii, Y.4
  • 33
    • 0019854279 scopus 로고
    • A pharmacokinetic analysis program (MULTI) for microcomputer
    • Yamaoka K, Tanigawara Y, Nakagawa T, and Uno T (1981) A pharmacokinetic analysis program (MULTI) for microcomputer. J Pharmacobio-Dyn 4:879-885.
    • (1981) J Pharmacobio-Dyn , vol.4 , pp. 879-885
    • Yamaoka, K.1    Tanigawara, Y.2    Nakagawa, T.3    Uno, T.4
  • 34
    • 0033007586 scopus 로고    scopus 로고
    • Dose-dependent plasma clearance of MK-826, a carbapenem antibiotic, arising from concentration-dependent plasma binding in rats and monkeys
    • Wong BK, Bruhin PJ, and Lin JH (1999) Dose-dependent plasma clearance of MK-826, a carbapenem antibiotic, arising from concentration-dependent plasma binding in rats and monkeys. J Pharm Sci 88:277-280.
    • (1999) J Pharm Sci , vol.88 , pp. 277-280
    • Wong, B.K.1    Bruhin, P.J.2    Lin, J.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.