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Volumn 25, Issue 12, 1997, Pages 1359-1369

Nonspecific binding to microsomes: Impact on scale-up of in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine, and propranolol

Author keywords

[No Author keywords available]

Indexed keywords

IMIPRAMINE; PROPRANOLOL DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; WARFARIN;

EID: 0031466149     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (277)

References (37)
  • 1
    • 0016566218 scopus 로고
    • A physiological approach to hepatic drug clearance
    • G. R. Wilkinson and D. G. Shand: A physiological approach to hepatic drug clearance. Clin. Pharmacol. Ther. 18, 377-390 (1975).
    • (1975) Clin. Pharmacol. Ther. , vol.18 , pp. 377-390
    • Wilkinson, G.R.1    Shand, D.G.2
  • 2
    • 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
    • K. S. Pang and M. Rowland: 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).
    • (1977) J. Pharmacokinet. Biopharm. , vol.5 , pp. 625-653
    • Pang, K.S.1    Rowland, M.2
  • 3
    • 0017335453 scopus 로고
    • Prediction of hepatic extraction ratio from in vitro measurement of intrinsic clearance
    • A. Rane, G. R. Wilkinson, and D. G. Shand: Prediction of hepatic extraction ratio from in vitro measurement of intrinsic clearance. J. Pharmacol. Exp. Ther. 200, 420-424 (1977).
    • (1977) J. Pharmacol. Exp. Ther. , vol.200 , pp. 420-424
    • Rane, A.1    Wilkinson, G.R.2    Shand, D.G.3
  • 4
    • 0028342648 scopus 로고
    • Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
    • J. B. Houston: Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance. Biochem. Pharmacol. 47, 1469-1479 (1994).
    • (1994) Biochem. Pharmacol. , vol.47 , pp. 1469-1479
    • Houston, J.B.1
  • 6
    • 0029071988 scopus 로고
    • Report on the international workshop on the use of human in vitro liver preparations to study drug metabolism in drug development
    • P. Skett, C. Tyson, A. Guillouzo, and P. Maier: Report on the international workshop on the use of human in vitro liver preparations to study drug metabolism in drug development. Biochem. Pharmacol. 50, 280-285 (1995).
    • (1995) Biochem. Pharmacol. , vol.50 , pp. 280-285
    • Skett, P.1    Tyson, C.2    Guillouzo, A.3    Maier, P.4
  • 7
    • 0029908277 scopus 로고    scopus 로고
    • The importance of nonspecific binding in in vitro matrices, its impact on enzyme kinetic studies of drug metabolism reactions, and implications for in vitro-in vivo correlations
    • R. S. Obach: The importance of nonspecific binding in in vitro matrices, its impact on enzyme kinetic studies of drug metabolism reactions, and implications for in vitro-in vivo correlations. Drug Metab. Dispos. 24, 1047-1049 (1996).
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 1047-1049
    • Obach, R.S.1
  • 8
    • 0022542635 scopus 로고
    • In vivo pharmacokinetics of felodipine predicted from in vitro studies in rat, dog, and man
    • C. Baarnhielm, H. Dahlback, and I. Skanberg: In vivo pharmacokinetics of felodipine predicted from in vitro studies in rat, dog, and man. Acta Pharmacol. Toxicol. 59, 113-122 (1986).
    • (1986) Acta Pharmacol. Toxicol. , vol.59 , pp. 113-122
    • Baarnhielm, C.1    Dahlback, H.2    Skanberg, I.3
  • 10
    • 0015451733 scopus 로고
    • Sodium warfarin
    • P. A. O'Reilly: Sodium warfarin. Pharmacology 8, 181-190 (1972).
    • (1972) Pharmacology , vol.8 , pp. 181-190
    • O'Reilly, P.A.1
  • 11
    • 0015723925 scopus 로고
    • Plasma binding of imipramine and clinical outcome
    • A. H. Glassman, M. J. Hurwic, and J. M. Perel: Plasma binding of imipramine and clinical outcome. Am. J. Psychiat. 130, 1367-1369 (1973).
    • (1973) Am. J. Psychiat. , vol.130 , pp. 1367-1369
    • Glassman, A.H.1    Hurwic, M.J.2    Perel, J.M.3
  • 12
    • 0021052764 scopus 로고
    • Imipramine serum protein binding in healthy subjects
    • C. B. Kristensen: Imipramine serum protein binding in healthy subjects. Clin. Pharmacol. Ther. 34, 689-694 (1983).
    • (1983) Clin. Pharmacol. Ther. , vol.34 , pp. 689-694
    • Kristensen, C.B.1
  • 13
    • 0025218419 scopus 로고
    • Clinical pharmacokinetics of imipramine and desipramine
    • F. R. Sallee and B. G. Pollack: Clinical pharmacokinetics of imipramine and desipramine. Clin. Pharmacokinet. 18, 346-364 (1990).
    • (1990) Clin. Pharmacokinet. , vol.18 , pp. 346-364
    • Sallee, F.R.1    Pollack, B.G.2
  • 14
    • 0018126170 scopus 로고
    • Correlation between in vitro and in vivo drug metabolism rate: Oxidation of ethoxybenzamide in rat
    • J. H. Lin, M. Hayashi, S. Awazu, and M. Hanano: Correlation between in vitro and in vivo drug metabolism rate: oxidation of ethoxybenzamide in rat. J. Pharmacokinet. Biopharm. 6, 327-337 (1978).
    • (1978) J. Pharmacokinet. Biopharm. , vol.6 , pp. 327-337
    • Lin, J.H.1    Hayashi, M.2    Awazu, S.3    Hanano, M.4
  • 15
    • 0018962319 scopus 로고
    • Kinetic studies on the deethylation of ethoxybenzamide: A comparative study with isolated hepatocytes and liver microsomes of rat
    • J. H. Lin, Y. Sugiyama, S. Awazu, and M. Hanano: Kinetic studies on the deethylation of ethoxybenzamide: a comparative study with isolated hepatocytes and liver microsomes of rat. Biochem. Pharmacol. 29, 2825-2830 (1980).
    • (1980) Biochem. Pharmacol. , vol.29 , pp. 2825-2830
    • Lin, J.H.1    Sugiyama, Y.2    Awazu, S.3    Hanano, M.4
  • 16
    • 0025279535 scopus 로고
    • Pharmacokinetic correlation between in vitro hepatic microsomal enzyme kinetics and in vivo metabolism of imipramine and desipramine in rats
    • M. Chiba, S. Fujita, and T. Suzuki: Pharmacokinetic correlation between in vitro hepatic microsomal enzyme kinetics and in vivo metabolism of imipramine and desipramine in rats. J. Pharm. Sci. 79, 281-287 (1990).
    • (1990) J. Pharm. Sci. , vol.79 , pp. 281-287
    • Chiba, M.1    Fujita, S.2    Suzuki, T.3
  • 17
    • 0029561539 scopus 로고
    • Concentration dependent metabolism of diazepam in the mouse
    • M. V. St. Pierre and K. S. Pang: Concentration dependent metabolism of diazepam in the mouse. J. Pharmacokinet. Biopharm. 23, 243-266 (1995).
    • (1995) J. Pharmacokinet. Biopharm. , vol.23 , pp. 243-266
    • St. Pierre, M.V.1    Pang, K.S.2
  • 19
    • 0015962809 scopus 로고
    • Binding of basic and acidic drugs to rat tissue subcellular fractions
    • M. H. Bickel and J. W. Steele: Binding of basic and acidic drugs to rat tissue subcellular fractions. Chem.-Biol. Interact. 8, 151-162 (1974).
    • (1974) Chem.-Biol. Interact. , vol.8 , pp. 151-162
    • Bickel, M.H.1    Steele, J.W.2
  • 20
    • 0017357703 scopus 로고
    • Membrane lipids as intracellular binders of chlorpromazine and related drugs
    • C. DiFrancesco and M. H. Bickel: Membrane lipids as intracellular binders of chlorpromazine and related drugs. Chem.-Biol. Interact. 16, 335-346 (1977).
    • (1977) Chem.-Biol. Interact. , vol.16 , pp. 335-346
    • DiFrancesco, C.1    Bickel, M.H.2
  • 21
    • 0028351919 scopus 로고
    • Metabolic kinetics of pseudoracemic propranolol in human liver microsomes: Enantioselectivity and quinidine inhibition
    • P. H. Marathe, D. D. Shen, and W. L. Nelson: Metabolic kinetics of pseudoracemic propranolol in human liver microsomes: enantioselectivity and quinidine inhibition. Drug Metab. Dispos. 22, 237-247 (1994).
    • (1994) Drug Metab. Dispos. , vol.22 , pp. 237-247
    • Marathe, P.H.1    Shen, D.D.2    Nelson, W.L.3
  • 22
    • 0024993542 scopus 로고
    • Propranolol oxidation by human liver microsomes-the use of cumene hydroperoxide to probe isoenzyme specificity and regio- and stereoselectivity
    • S. V. Otton, E. M. J. Gillam, M. S. Lennard, G. T. Tucker, and H. F. Woods: Propranolol oxidation by human liver microsomes-the use of cumene hydroperoxide to probe isoenzyme specificity and regio- and stereoselectivity. Br. J. Clin. Pharmacol. 30, 751-760 (1990).
    • (1990) Br. J. Clin. Pharmacol. , vol.30 , pp. 751-760
    • Otton, S.V.1    Gillam, E.M.J.2    Lennard, M.S.3    Tucker, G.T.4    Woods, H.F.5
  • 23
    • 0024403279 scopus 로고
    • Characteristics of warfarin hydroxylation catalyzed by human liver microsomes
    • A. E. Rettie, A. C. Eddy, L. D. Heimark, M. Gibaldi, and W. F. Trager: Characteristics of warfarin hydroxylation catalyzed by human liver microsomes. Drug Metab. Dispos. 17, 265-270 (1989).
    • (1989) Drug Metab. Dispos. , vol.17 , pp. 265-270
    • Rettie, A.E.1    Eddy, A.C.2    Heimark, L.D.3    Gibaldi, M.4    Trager, W.F.5
  • 26
    • 0028214359 scopus 로고
    • The role of S-mephenytoin 4′-hydroxylase in imipramine metabolism by human liver microsomes: A two-enzyme kinetic analysis of N-demethylation and 2-hydroxylation
    • K. Chiba, A. Saitoh, E. Koyama, M. Tani, M. Hayashi, and T. Ishizaki: The role of S-mephenytoin 4′-hydroxylase in imipramine metabolism by human liver microsomes: a two-enzyme kinetic analysis of N-demethylation and 2-hydroxylation. Br. J. Clin. Pharmacol. 37, 237-242 (1994).
    • (1994) Br. J. Clin. Pharmacol. , vol.37 , pp. 237-242
    • Chiba, K.1    Saitoh, A.2    Koyama, E.3    Tani, M.4    Hayashi, M.5    Ishizaki, T.6
  • 27
    • 0026795695 scopus 로고
    • Inhibitors of imipramine metabolism by human liver microsomes
    • E. Skjelbo and K. Brosen: Inhibitors of imipramine metabolism by human liver microsomes. Br. J. Clin. Pharmacol. 34, 256-261 (1992).
    • (1992) Br. J. Clin. Pharmacol. , vol.34 , pp. 256-261
    • Skjelbo, E.1    Brosen, K.2
  • 29
    • 0028228640 scopus 로고
    • Disposition of warfarin enantiomers and metabolites in patients during multiple dosing with rac-warfarin
    • E. Chan, A. J. McLachlan, M. Pegg, A. D. MacKay, R. B. Cole, and M. Rowland: Disposition of warfarin enantiomers and metabolites in patients during multiple dosing with rac-warfarin. Br. J. Clin. Pharmacol. 37, 563-569 (1994).
    • (1994) Br. J. Clin. Pharmacol. , vol.37 , pp. 563-569
    • Chan, E.1    McLachlan, A.J.2    Pegg, M.3    MacKay, A.D.4    Cole, R.B.5    Rowland, M.6
  • 31
    • 0026092176 scopus 로고
    • Metabolic enantiomeric interaction: The inhibition of human (S)-warfann-7-hydroxylase by (R)-warfarin
    • K. L. Kunze, A. C. Eddy, M. Gibaldi, and W. F. Trager: Metabolic enantiomeric interaction: The inhibition of human (S)-warfann-7-hydroxylase by (R)-warfarin. Chirality 3, 24-29 (1991).
    • (1991) Chirality , vol.3 , pp. 24-29
    • Kunze, K.L.1    Eddy, A.C.2    Gibaldi, M.3    Trager, W.F.4
  • 32
    • 0020348530 scopus 로고
    • Pharmacokinetic aspects of some §-adrenoceptor blocking drugs
    • C. G. Regardh: Pharmacokinetic aspects of some §-adrenoceptor blocking drugs. Acta Med. Scand. 665, 49-60 (1982).
    • (1982) Acta Med. Scand. , vol.665 , pp. 49-60
    • Regardh, C.G.1
  • 33
    • 0021917028 scopus 로고
    • Quantitative account of propranolol metabolism in urine of normal man
    • T. Walle, U. K. Walle, and L. S. Olanoff: Quantitative account of propranolol metabolism in urine of normal man. Drug Metab. Dispos. 13, 204-209 (1985).
    • (1985) Drug Metab. Dispos. , vol.13 , pp. 204-209
    • Walle, T.1    Walle, U.K.2    Olanoff, L.S.3
  • 34
    • 0022994696 scopus 로고
    • Partial metabolic clearances as determinants of the oral bioavailability of propranolol
    • T. Walle, U. K. Walle, L. S. Olanoff, and E. C. Conradi: Partial metabolic clearances as determinants of the oral bioavailability of propranolol. Br. J. Clin. Pharmacol. 22, 317-323 (1986).
    • (1986) Br. J. Clin. Pharmacol. , vol.22 , pp. 317-323
    • Walle, T.1    Walle, U.K.2    Olanoff, L.S.3    Conradi, E.C.4
  • 35
    • 0029027857 scopus 로고
    • Prediction of in vivo disposition from in vitro systems: Clearance of phenytoin and tolbutamide using rat hepatic microsomal and hepatocyte data
    • E. I. L. Ashforth, D. J. Carlile, R. Chenery, and J. B. Houston: Prediction of in vivo disposition from in vitro systems: clearance of phenytoin and tolbutamide using rat hepatic microsomal and hepatocyte data. J. Pharmacol. Exp. Ther. 274, 761-766 (1995).
    • (1995) J. Pharmacol. Exp. Ther. , vol.274 , pp. 761-766
    • Ashforth, E.I.L.1    Carlile, D.J.2    Chenery, R.3    Houston, J.B.4
  • 36
    • 0030345024 scopus 로고    scopus 로고
    • (S)-4′-Hydroxypropranolol causes product inhibition and dose-dependent bioavailability of propranolol enantiomers in the isolated perfused rat liver and in rat liver microsomes
    • R. A. Nand, H. Ghabrial, R. A. Smallwood, and D. J. Morgan: (S)-4′-Hydroxypropranolol causes product inhibition and dose-dependent bioavailability of propranolol enantiomers in the isolated perfused rat liver and in rat liver microsomes. Xenobiotica 26, 1249-1261 (1996).
    • (1996) Xenobiotica , vol.26 , pp. 1249-1261
    • Nand, R.A.1    Ghabrial, H.2    Smallwood, R.A.3    Morgan, D.J.4
  • 37
    • 0016817127 scopus 로고
    • Studies on a ketone reductase in human and rat liver and kidney soluble fraction using warfarin as a substrate
    • T. A. Moreland and D. S. Hewick: Studies on a ketone reductase in human and rat liver and kidney soluble fraction using warfarin as a substrate. Biochem. Pharmacol. 24, 1953-1957 (1975).
    • (1975) Biochem. Pharmacol. , vol.24 , pp. 1953-1957
    • Moreland, T.A.1    Hewick, D.S.2


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