Estimation of tissue-to-plasma partition coefficients used in physiological pharmacokinetic models
- PMID: 458554
- DOI: 10.1007/BF01059446
Estimation of tissue-to-plasma partition coefficients used in physiological pharmacokinetic models
Abstract
An important parameter in the development of pharmacokinetic models is the ratio of tissue drug concentration to the concentration of the drug in the arterial plasma or the effluent plasma. The relationship between these two tissue/plasma ratios is derived analytically for different routes of drug administration. The two are equal only in compartments with no elimination when the drug is infused at constant rate. For other routes of administration, the two ratios are identical in all compartments only when there is no elimination process. The tissue/plasma concentration ratios for infusion equilibrium are not equal to the corresponding values for the postdistribution phase after an intravenous bolus injection. When the plasma concentration for infusion and injection are the same, more drug will appear in the lung during infusion steady state than during the postdistribution equilibrium. The reverse is true for the other organs. The importance of properly defining the tissue/plasma ratio and its implication for pharmacokinetic modeling are discussed. The results may have important therapeutic implications for the availability of drugs using different routes of administration.
Similar articles
-
Determination of tissue to blood partition coefficients in physiologically-based pharmacokinetic studies.J Pharm Sci. 1982 Apr;71(4):454-6. doi: 10.1002/jps.2600710421. J Pharm Sci. 1982. PMID: 7086658
-
On the accuracy of estimation of basic pharmacokinetic parameters by the traditional noncompartmental equations and the prediction of the steady-state volume of distribution in obese patients based upon data derived from normal subjects.J Pharm Sci. 2011 Jun;100(6):2482-97. doi: 10.1002/jps.22444. Epub 2011 Jan 19. J Pharm Sci. 2011. PMID: 21254063
-
Steady-state plasma concentrations as a function of the absorption rate and dosing interval for drugs exhibiting concentration-dependent clearance: consequences for phenytoin therapy.J Pharmacokinet Biopharm. 1979 Dec;7(6):543-55. doi: 10.1007/BF01061208. J Pharmacokinet Biopharm. 1979. PMID: 529023
-
Is volume of distribution at steady state a meaningful kinetic variable?J Clin Pharmacol. 1983 Aug-Sep;23(8-9):391-400. doi: 10.1002/j.1552-4604.1983.tb02753.x. J Clin Pharmacol. 1983. PMID: 6355205 Review.
-
Drug dosage in renal disease.Clin Pharmacokinet. 1976;1(2):126-34. doi: 10.2165/00003088-197601020-00004. Clin Pharmacokinet. 1976. PMID: 797495 Review.
Cited by
-
A semiparametric approach to physiological flow models.J Pharmacokinet Biopharm. 1989 Aug;17(4):463-91. doi: 10.1007/BF01061458. J Pharmacokinet Biopharm. 1989. PMID: 2614682
-
Physiologically based pharmacokinetic modeling of SNU-0039, an anti-Alzheimer's agent, in rats.J Pharmacokinet Pharmacodyn. 2011 Oct;38(5):637-51. doi: 10.1007/s10928-011-9212-6. Epub 2011 Aug 25. J Pharmacokinet Pharmacodyn. 2011. PMID: 21866408
-
Disposition of azole antifungal agents. II. Hepatic binding and clearance of dichlorophenyl-bis-triazolylpropanol (DTP) in the rat.Pharm Res. 1994 Jul;11(7):951-60. doi: 10.1023/a:1018966800208. Pharm Res. 1994. PMID: 7937554
-
Disposition of azole antifungal agents. I. Nonlinearities in ketoconazole clearance and binding in rat liver.Pharm Res. 1993 Mar;10(3):418-22. doi: 10.1023/a:1018996524141. Pharm Res. 1993. PMID: 8464816
-
Comparative physiologically based pharmacokinetics of hexobarbital, phenobarbital and thiopental in the rat.J Pharmacokinet Biopharm. 1982 Feb;10(1):53-75. doi: 10.1007/BF01059183. J Pharmacokinet Biopharm. 1982. PMID: 7069578