Literature DB >> 1133714

Nonliner tissue disposition: salicylic acid in rat brain.

M A Gonzalez, T N Tozer, T T Chang.   

Abstract

A model was developed to detect nonlinear disposition of a drug in a tissue. The model was experimentally tested relating to salicylic acid disposition in the brain. Experimental data obtained in rats are reported for doses of 25 and 40 mg/kg ip. The parameters measured for each dose were the ratio of the area under the brain concentration-time curve to the area under the plasma concentration-time curve and the ratio of the maximum brain concentration of salicylic acid to the plasma concentration at that point in time. The ratios increased with dose; furthermore, ratios calculated using plasma concentrations corrected for plasma protein binding were dose dependent. Calculations performed on literature data for salicylic acid disposition in mouse brain corroborated the results of this sutdy. The existence of a saturable transport system for the elimination of salicylic acid from the brain is supported by the data presented. The rationale necessary to apply the model to any tissue is discussed.

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Year:  1975        PMID: 1133714     DOI: 10.1002/jps.2600640120

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  7 in total

1.  Potential gamma-hydroxybutyric acid (GHB) drug interactions through blood-brain barrier transport inhibition: a pharmacokinetic simulation-based evaluation.

Authors:  Indranil Bhattacharya; Kathleen M K Boje
Journal:  J Pharmacokinet Pharmacodyn       Date:  2006-08-29       Impact factor: 2.745

2.  In vivo specific binding characteristics and pharmacokinetics of a 1,4-dihydropyridine calcium channel antagonist in the senescent mouse brain.

Authors:  S Uchida; S Yamada; Y Deguchi; M Yamamoto; R Kimura
Journal:  Pharm Res       Date:  2000-07       Impact factor: 4.200

3.  Mode of action of tiaspirone on the central cholinergic system.

Authors:  K Kolasa; E Palazzi; P Salmoiraghi; G Guiso; S Caccia; S Garattini; S Consolo
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-09       Impact factor: 3.000

4.  Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred" model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearance.

Authors:  K S Pang; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1977-12

5.  Kinetics and brain uptake of S 9795, a new xanthine derivate, in rats.

Authors:  G Bianchi; S Caccia; F Della Vedova; S Garattini
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1989 Jul-Sep       Impact factor: 2.441

6.  Pharmacological studies in the rat with [2-(1,3-didecanoyloxy)-propyl]2-acetyloxybenzoate (A-45474): an aspirin pro-drug with negligible gastric irritation.

Authors:  G W Carter; P R Young; L R Swett; G Y Paris
Journal:  Agents Actions       Date:  1980-06

7.  Modeling the enhanced uptake of zidovudine (AZT) into cerebrospinal fluid. 1. Effect of probenecid.

Authors:  R J Sawchuk; M A Hedaya
Journal:  Pharm Res       Date:  1990-04       Impact factor: 4.200

  7 in total

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