Literature DB >> 6533295

Concentration and pH dependent steady-state volume of distribution of methotrexate estimated by a simple physiologically based method.

C Y Lui, M G Lee, W L Chiou.   

Abstract

The effects of plasma concentration and pH on the steady-state volume of distribution, Vss, of methotrexate (MTX) were studied in five conditioned male beagle-mongrel dogs. Steady-state plasma MTX concentrations of approximately 1, 20, and 100 micrograms/ml were targeted for by i.v. bolus doses followed by i.v. infusions. An isotonic solution of sodium bicarbonate or ammonium chloride was simultaneously infused for the purpose of inducing plasma pH change, while the infusion of an isotonic solution of sodium chloride served as a control. Plasma and urine concentrations of MTX were quantitated by a sensitive high-performance liquid chromatographic method, and the Vss of MTX was estimated by a recently reported physiologically based method of Chiou and Lam. Statistically significant (p less than 0.05) concentration and plasma pH dependent Vss of MTX were observed. Concentration dependence of Vss was noted in sodium chloride and ammonium chloride infused dogs, but not in bicarbonate treated dogs. There was an average 50.0 and 44.8% increase in Vss at 1 microgram/ml relative to the two higher concentrations (20 and 100 micrograms/ml) for dogs treated with ammonium and sodium chloride, respectively. However, Vss of MTX at the targeted concentrations of 20 and 100 micrograms/ml was relatively constant. Plasma pH dependence of Vss was observed only at the plasma concentration of 1 microgram/ml, and on the average, ammonium chloride and sodium chloride treatments resulted in 50.0 and 31.3% higher Vss, respectively, when compared with the bicarbonate treatment. These phenomena appear to be adequately explained by the reported tissue uptake kinetics of MTX.

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Year:  1984        PMID: 6533295     DOI: 10.1007/bf01059555

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


  32 in total

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Authors:  J W JAILER; C G ZUBROD
Journal:  J Pharmacol Exp Ther       Date:  1948-03       Impact factor: 4.030

2.  The fate of thiopental in man and a method for its estimation in biological material.

Authors:  B B BRODIE; L C MARK
Journal:  J Pharmacol Exp Ther       Date:  1950-01       Impact factor: 4.030

3.  A pH-dependent, carrier-mediated transport system for the folate analog, amethopterin, in rat jejunum.

Authors:  W B Strum
Journal:  J Pharmacol Exp Ther       Date:  1977-12       Impact factor: 4.030

4.  A specific HPLC assay to determine the pharmacokinetics of methotrexate in patients.

Authors:  M L Chen; W P McGuire; T E Lad; W L Chiou
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1984-01

5.  Effect of arterial-venous plasma concentration differences on the determination of mean residence time of drugs in the body.

Authors:  W L Chiou; G Lam; M L Chen; M G Lee
Journal:  Res Commun Chem Pathol Pharmacol       Date:  1982-01

6.  Pharmacokinetics of drugs in blood. I. Unusual distribution of gentamicin.

Authors:  M G Lee; M L Chen; S M Huang; W L Chiou
Journal:  Biopharm Drug Dispos       Date:  1981 Jan-Mar       Impact factor: 1.627

7.  Renal tubular transport of methotrexate in the rhesus monkey and dog.

Authors:  K C Huang; B A Wenczak; Y K Liu
Journal:  Cancer Res       Date:  1979-12       Impact factor: 12.701

8.  Methotrexate serum and saliva concentrations in patients.

Authors:  A J Patterson; W A Ritschel; D Zellner; S H Kim
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1981-09

9.  Sensitive and rapid high-performance liquid chromatographic method for the simultaneous determination of methotrexate and its metabolites in plasma, saliva and urine.

Authors:  M L Chen; W L Chiou
Journal:  J Chromatogr       Date:  1981-11-13

10.  Genetically alterable transport of amethopterin in Diplococcus pneumoniae. I. Physiological properties and kinetics of the wild-type system.

Authors:  F M Sirotnak; M G Sargent; D J Hutchison
Journal:  J Bacteriol       Date:  1967-01       Impact factor: 3.490

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  4 in total

Review 1.  The phenomenon and rationale of marked dependence of drug concentration on blood sampling site. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics (Part II).

Authors:  W L Chiou
Journal:  Clin Pharmacokinet       Date:  1989-10       Impact factor: 6.447

2.  Effects of cilastatin on the pharmacokinetics of a new carbapenem, DA-1131, in rats, rabbits, and dogs.

Authors:  S H Kim; J W Kwon; W B Kim; M G Lee
Journal:  Antimicrob Agents Chemother       Date:  1999-10       Impact factor: 5.191

3.  Prognostic importance of systemic clearance of methotrexate in childhood acute lymphoblastic leukemia.

Authors:  J D Borsi; T Revesz; D Schuler
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

4.  Effects of the rate and composition of fluid replacement on the pharmacokinetics and pharmacodynamics of intravenous furosemide.

Authors:  T Li; M G Lee; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1986-10
  4 in total

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