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PUBMED FOR HANDHELDS

Journal Abstract Search


179 related items for PubMed ID: 8410683

  • 41. PBPK modeling to unravel nonlinear pharmacokinetics of verapamil to estimate the fractional clearance for verapamil N-demethylation in the recirculating rat liver preparation.
    Yang QJ, Si L, Tang H, Sveigaard HH, Chow EC, Pang KS.
    Drug Metab Dispos; 2015 Apr; 43(4):631-45. PubMed ID: 25650380
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  • 42. Correlation of drug conjugative metabolism rates between in vivo and in vitro: glucuronidation and sulfation of p-nitrophenol as a model compound in rat.
    Mizuma T, Machida M, Hayashi M, Awazu S.
    J Pharmacobiodyn; 1982 Oct; 5(10):811-7. PubMed ID: 7161709
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  • 43. Membrane transport in hepatic clearance of drugs. I: Extended hepatic clearance models incorporating concentration-dependent transport and elimination processes.
    Kwon Y, Morris ME.
    Pharm Res; 1997 Jun; 14(6):774-9. PubMed ID: 9210196
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  • 47. Hepatic elimination of drugs with concentration-dependent serum protein binding.
    Huang JD, Oie S.
    J Pharmacokinet Biopharm; 1984 Feb; 12(1):67-81. PubMed ID: 6747819
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  • 50. After 50 Years of Hepatic Clearance Models, Where Should We Go from Here? Improvements and Implications for Physiologically Based Pharmacokinetic Modeling.
    Pang KS, Lu WI, Mulder GJ.
    Drug Metab Dispos; 2024 Jul 16; 52(8):919-931. PubMed ID: 39013583
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  • 52. Nonlinear elimination and hepatic concentration of conjugation-metabolite of valproate in guinea-pigs.
    Yu HY, Wu MS, Shen YZ.
    Biopharm Drug Dispos; 1993 May 16; 14(4):297-312. PubMed ID: 8499581
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  • 53. Physiologic models of hepatic drug clearance: influence of altered protein binding on the elimination of diclofenac in the isolated perfused rat liver.
    Hussein Z, Evans AM, Rowland M.
    J Pharm Sci; 1993 Sep 16; 82(9):880-5. PubMed ID: 8229684
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  • 54. Disposition of glycyrrhizin in the perfused liver of rats.
    Ishida S, Sakiya Y, Taira Z.
    Biol Pharm Bull; 1994 Jul 16; 17(7):960-9. PubMed ID: 8000386
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