Literature DB >> 3668804

Area method for the estimation of partition coefficients for physiological pharmacokinetic models.

J M Gallo1, F C Lam, D G Perrier.   

Abstract

A new technique, the area method, is derived for the determination of partition coefficients for both blood-flow limited and membrane limited physiological pharmacokinetic models. This method was compared to a standard technique by Monte Carlo simulation. Partition coefficients were calculated for the blood-flow limited case for both eliminating and noneliminating organs. It was found that the area method compared favorably to a standard technique and was less prone to error. This may be attributed to the more subjective interpretation as to which data points are included in the terminal phase, since the standard method relies on the accurate determination of the terminal slope for the calculation of partition coefficients. Both methods are satisfactory for the calculation of partition coefficients with the area method being more accurate and precise.

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Year:  1987        PMID: 3668804     DOI: 10.1007/bf01066322

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  6 in total

1.  Estimation of tissue-to-plasma partition coefficients used in physiological pharmacokinetic models.

Authors:  H S Chen; J F Gross
Journal:  J Pharmacokinet Biopharm       Date:  1979-02

Review 2.  Physiologically based pharmacokinetic modeling: principles and applications.

Authors:  L E Gerlowski; R K Jain
Journal:  J Pharm Sci       Date:  1983-10       Impact factor: 3.534

3.  Physiologic model for the pharmacokinetics of 2'deoxycoformycin in normal and leukemic mice.

Authors:  F G King; R L Dedrick
Journal:  J Pharmacokinet Biopharm       Date:  1981-10

Review 4.  Physiological pharmacokinetics: an in vivo approach to membrane transport.

Authors:  R J Lutz; R L Dedrick; D S Zaharko
Journal:  Pharmacol Ther       Date:  1980       Impact factor: 12.310

5.  In vitro and in vivo evaluation of the tissue-to-blood partition coefficient for physiological pharmacokinetic models.

Authors:  J H Lin; Y Sugiyama; S Awazu; M Hanano
Journal:  J Pharmacokinet Biopharm       Date:  1982-12

6.  A physiologically based pharmacokinetic model for theophylline disposition in the pregnant and nonpregnant rat.

Authors:  J L Gabrielsson; L K Paalzow; L Nordström
Journal:  J Pharmacokinet Biopharm       Date:  1984-04
  6 in total
  19 in total

1.  Quantitative structure-pharmacokinetics relationships: II. A mechanistically based model to evaluate the relationship between tissue distribution parameters and compound lipophilicity.

Authors:  I Nestorov; L Aarons; M Rowland
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Review 2.  Whole body pharmacokinetic models.

Authors:  Ivan Nestorov
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

3.  Physiological pharmacokinetic model of adriamycin delivered via magnetic albumin microspheres in the rat.

Authors:  J M Gallo; C T Hung; P K Gupta; D G Perrier
Journal:  J Pharmacokinet Biopharm       Date:  1989-06

4.  Development of a whole body physiologically based model to characterise the pharmacokinetics of benzodiazepines. 1: Estimation of rat tissue-plasma partition ratios.

Authors:  Ivelina Gueorguieva; Ivan A Nestorov; Susan Murby; Sophie Gisbert; Brent Collins; Kelly Dickens; Judith Duffy; Ziad Hussain; Malcolm Rowland
Journal:  J Pharmacokinet Pharmacodyn       Date:  2004-08       Impact factor: 2.745

5.  A comment on the application of drug tissue-plasma partition coefficients K(p) in eliminating organs to calculation of volume of distribution at steady state.

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Journal:  J Pharmacokinet Pharmacodyn       Date:  2005-12       Impact factor: 2.745

6.  A semiparametric approach to physiological flow models.

Authors:  D Verotta; L B Sheiner; W F Ebling; D R Stanski
Journal:  J Pharmacokinet Biopharm       Date:  1989-08

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Journal:  J Pharm Sci       Date:  2011-10-03       Impact factor: 3.534

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Authors:  Gerald J Fetterly; Robert M Straubinger
Journal:  AAPS PharmSci       Date:  2003-11-21

10.  Physiologically based pharmacokinetics of matrine in the rat after oral administration of pure chemical and ACAPHA.

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Journal:  Drug Metab Dispos       Date:  2009-01-08       Impact factor: 3.922

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