Literature DB >> 24178037

On the maintenance of hepatocyte intracellular pH 7.0 in the in-vitro metabolic stability assay.

Leonid M Berezhkovskiy1, Susan Wong, Jason S Halladay.   

Abstract

The account of pH difference between hepatocytes (intracellular pH 7.0) and extracellular water (pH 7.4) leads to the novel equation for hepatic clearance (Berezhkovskiy, J Pharma Sci 100:1167-1683, 2011). The metabolic stability assay using hepatocytes is commonly performed in the incubation buffer of pH 7.4. If hepatocytes retain their physiological pH 7.0 in these conditions, then the assay would mimic the in vivo condition, that is pH 7.4 for plasma and extracellular water, and pH 7.0 in hepatocytes. In this case the rate of drug elimination, taken as proportional to unbound drug concentration in buffer, would correspond to the in vivo rate of drug elimination as proportional to the unbound drug concentration in the extracellular water. Consequently the commonly used PBPK equation for the rate of hepatic elimination, and the equation for hepatic clearance would be valid. However, the experiment designed to determine hepatocyte internal pH indicated that it was not maintained in the in vitro stability assay, so that hepatocytes acquire the same pH as the incubation buffer. Thus, the novel equations for hepatic clearance (that include an ionization factor) should be applied regardless if the intrinsic clearance was obtained either from microsomal or hepatocyte stability assay.

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Year:  2013        PMID: 24178037     DOI: 10.1007/s10928-013-9339-8

Source DB:  PubMed          Journal:  J Pharmacokinet Pharmacodyn        ISSN: 1567-567X            Impact factor:   2.745


  10 in total

1.  Evaluation of fresh and cryopreserved hepatocytes as in vitro drug metabolism tools for the prediction of metabolic clearance.

Authors:  Dermot F McGinnity; Matthew G Soars; Richard A Urbanowicz; Robert J Riley
Journal:  Drug Metab Dispos       Date:  2004-07-30       Impact factor: 3.922

2.  Consistency of the novel equations for determination of hepatic clearance and drug time course in liver that account for the difference in drug ionization in extracellular and intracellular tissue water.

Authors:  Leonid M Berezhkovskiy; Ning Liu; Jason S Halladay
Journal:  J Pharm Sci       Date:  2011-11-23       Impact factor: 3.534

3.  Physiologically based pharmacokinetic modelling 2: predicting the tissue distribution of acids, very weak bases, neutrals and zwitterions.

Authors:  Trudy Rodgers; Malcolm Rowland
Journal:  J Pharm Sci       Date:  2006-06       Impact factor: 3.534

Review 4.  Kinetic determinants of hepatic clearance: plasma protein binding and hepatic uptake.

Authors:  M Baker; T Parton
Journal:  Xenobiotica       Date:  2007 Oct-Nov       Impact factor: 1.908

5.  Saturable uptake of lipophilic amine drugs into isolated hepatocytes: mechanisms and consequences for quantitative clearance prediction.

Authors:  David Hallifax; J Brian Houston
Journal:  Drug Metab Dispos       Date:  2007-04-30       Impact factor: 3.922

6.  On the prediction of hepatic clearance using the diluted plasma in metabolic stability assay.

Authors:  Leonid M Berezhkovskiy; S Cyrus Khojasteh; Jason S Halladay; Cornelis E C A Hop
Journal:  J Pharm Sci       Date:  2009-06       Impact factor: 3.534

7.  The corrected traditional equations for calculation of hepatic clearance that account for the difference in drug ionization in extracellular and intracellular tissue water and the corresponding corrected PBPK equation.

Authors:  Leonid M Berezhkovskiy
Journal:  J Pharm Sci       Date:  2011-03       Impact factor: 3.534

8.  Noninvasive measurement of the pH of the endoplasmic reticulum at rest and during calcium release.

Authors:  J H Kim; L Johannes; B Goud; C Antony; C A Lingwood; R Daneman; S Grinstein
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

9.  A dispersion model of hepatic elimination: 2. Steady-state considerations--influence of hepatic blood flow, binding within blood, and hepatocellular enzyme activity.

Authors:  M S Roberts; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1986-06

10.  Intracellular pH of hepatocytes in primary monolayer culture.

Authors:  A S Pollock
Journal:  Am J Physiol       Date:  1984-05
  10 in total
  1 in total

1.  Physiology-based IVIVE predictions of tramadol from in vitro metabolism data.

Authors:  Huybrecht T'jollyn; Jan Snoeys; Pieter Colin; Jan Van Bocxlaer; Pieter Annaert; Filip Cuyckens; An Vermeulen; Achiel Van Peer; Karel Allegaert; Geert Mannens; Koen Boussery
Journal:  Pharm Res       Date:  2014-07-22       Impact factor: 4.200

  1 in total

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