Literature DB >> 7429676

Prediction of the volume of distribution from in vitro data and use for estimating the absolute extent of absorption.

W A Ritschel, G V Hammer.   

Abstract

The relationship between the volume of distribution, delta', extent of protein binding, EPB, and the apparent partition coefficient, APC, was investigated using 125 different drugs for which the data were retrieved from the literature, calculated, or determined experimentally. Equations were developed which allow one to predict the blood level concentration of a drug knowing the EPB, APC, and certain pharmacokinetic rate constants. Examples from the literature were cited in order to verify these equations. The delta-APC-EPB relationship can be used to estimate a drug's volume of distribution in a patient from in vitro data, and estimate the extent of absorption of extravascularly given drugs when I.V. data cannot be obtained.

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Year:  1980        PMID: 7429676

Source DB:  PubMed          Journal:  Int J Clin Pharmacol Ther Toxicol        ISSN: 0174-4879


  11 in total

1.  The effect of blood sampling site and physicochemical characteristics of drugs on bioavailability after nasal administration in the sheep model.

Authors:  L Illum; M Hinchcliffe; S S Davis
Journal:  Pharm Res       Date:  2003-09       Impact factor: 4.200

2.  The effect of E. coli STa enterotoxin on the absorption of weakly dissociable drugs from rat proximal jejunum in vivo.

Authors:  G T McEwan; M L Lucas
Journal:  Br J Pharmacol       Date:  1990-12       Impact factor: 8.739

Review 3.  Relationships between CSF drug concentrations, receptor binding characteristics, and pharmacokinetic and pharmacodynamic properties of selected 1,4-substituted benzodiazepines.

Authors:  W A Colburn; M L Jack
Journal:  Clin Pharmacokinet       Date:  1987-09       Impact factor: 6.447

Review 4.  Lorazepam: a review of its clinical pharmacological properties and therapeutic uses.

Authors:  B Ameer; D J Greenblatt
Journal:  Drugs       Date:  1981-03       Impact factor: 9.546

5.  Prediction of hepatic first-pass metabolism and plasma levels following intravenous and oral administration of barbiturates in the rabbit based on quantitative structure-pharmacokinetic relationships.

Authors:  N Watari; Y Sugiyama; N Kaneniwa; M Hiura
Journal:  J Pharmacokinet Biopharm       Date:  1988-06

6.  Relationships in the structure-tissue distribution of basic drugs in the rabbit.

Authors:  K Yokogawa; E Nakashima; J Ishizaki; H Maeda; T Nagano; F Ichimura
Journal:  Pharm Res       Date:  1990-07       Impact factor: 4.200

7.  Quantitative structure--pharmacokinetic relationship of a series of sulfonamides in the rat.

Authors:  S Kaul; W A Ritschel
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1990 Jul-Sep       Impact factor: 2.441

8.  The pharmacokinetics and bioavailability of a tracer dose of [3H]-mebendazole in man.

Authors:  M Dawson; P A Braithwaite; M S Roberts; T R Watson
Journal:  Br J Clin Pharmacol       Date:  1985-01       Impact factor: 4.335

9.  Clinical pharmacokinetics of high dose mebendazole in patients treated for cystic hydatid disease.

Authors:  P A Braithwaite; M S Roberts; R J Allan; T R Watson
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

10.  Pharmacokinetics of single doses of sulphinpyrazone and its major metabolites in plasma and urine.

Authors:  I D Bradbrook; V A John; P J Morrison; H J Rogers; R G Spector
Journal:  Br J Clin Pharmacol       Date:  1982-02       Impact factor: 4.335

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