Literature DB >> 7341756

Pharmacokinetics and tissue distribution of chlorpheniramine in rabbits after intravenous administration.

S M Huang, W L Chiou.   

Abstract

Intravenous studies of chlorpheniramine (CPM) were conducted in six New Zealand White male rabbits (mean wt. 3.88 kg). CPM and its two demethylated metabolites in arterial serum and urine were assayed by HPLC. Triexponential equations were needed to fit the i.v. CMP serum data in three rabbits, while biexponential equations were required in the other three rabbits. Harmonic mean of V1, Mss, Varea, CL, and terminal t 1/2 were 2.84, 10.8, and 15.5 liters/kg, and 4.14 liters/kg/hr and 2.57 hr, respectively. The average serum protein binding was 44%. The average blood to plasma concentration ratio was 1.85. Estimated mean hepatic blood extraction ratio based on i.v. studies was 0.88. Tissue distribution studies showed rapid and extensive uptake of CPM by various organs such as lung, kidneys, and brain after i.v. bolus injection, and their concentrations were 160-, 80-, and 31-fold higher than the plasma level. The amount of CPM in the muscle was calculated to represent about 50% of CPM present in the body near the steady state. Variation in plasma protein and tissue binding was postulated to be an important factor for the observed marked interspecies difference in the apparent volume of distribution of CPM. Only 2% of the dose was excreted unchanged in the urine.

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Year:  1981        PMID: 7341756     DOI: 10.1007/bf01070902

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


  28 in total

1.  Simplified gas chromatographic method for the determination of chlorpheniramine in serum.

Authors:  J W Barnhart; J D Johnson
Journal:  Anal Chem       Date:  1977-06       Impact factor: 6.986

2.  GLC determination of chlorpheniramine in human plasma.

Authors:  S Hanna; A Tang
Journal:  J Pharm Sci       Date:  1974-12       Impact factor: 3.534

3.  Metabolism of chlorpheniramine maleate in man.

Authors:  E A Peets; M Jackson; S Symchowicz
Journal:  J Pharmacol Exp Ther       Date:  1972-02       Impact factor: 4.030

4.  The metabolism of chlorpheniramine maleate in the dog and rat.

Authors:  E A Peets; R Weinstein; W Billard; S Symchowicz
Journal:  Arch Int Pharmacodyn Ther       Date:  1972-09

5.  Application of Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equations.

Authors:  K Yamaoka; T Nakagawa; T Uno
Journal:  J Pharmacokinet Biopharm       Date:  1978-04

6.  Critical evaluation of the potential error in pharmacokinetic studies of using the linear trapezoidal rule method for the calculation of the area under the plasma level--time curve.

Authors:  W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1978-12

7.  Potential effect of early blood sampling schedule on calculated pharmacokinetic parameters of drugs after intravenous administration.

Authors:  W L Chiou
Journal:  J Pharm Sci       Date:  1980-07       Impact factor: 3.534

8.  Sensitive GLC-mass spectrometric determination of chlorpheniramine in serum.

Authors:  J A Thompson; F H Leffert
Journal:  J Pharm Sci       Date:  1980-06       Impact factor: 3.534

9.  New calculation method for mean apparent drug volume of distribution and application to rational dosage regimens.

Authors:  W L Chiou
Journal:  J Pharm Sci       Date:  1979-08       Impact factor: 3.534

10.  Pharmocokinetics of hexobarbital in man after intravenous infusion.

Authors:  D D Breimer; C Honhoff; W Zilly; E Richter; J M van Rossum
Journal:  J Pharmacokinet Biopharm       Date:  1975-02
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  9 in total

1.  Dynamics of drug distribution. I. Role of the second and third curve moments.

Authors:  M Weiss; K S Pang
Journal:  J Pharmacokinet Biopharm       Date:  1992-06

2.  Prediction of the volumes of distribution of basic drugs in humans based on data from animals.

Authors:  Y Sawada; M Hanano; Y Sugiyama; H Harashima; T Iga
Journal:  J Pharmacokinet Biopharm       Date:  1984-12

3.  Erythrocytes as barriers for drug elimination in the isolated rat liver. II. Propranolol.

Authors:  H J Lee; W L Chiou
Journal:  Pharm Res       Date:  1989-10       Impact factor: 4.200

4.  Block of HERG k channel by classic histamine h(1) receptor antagonist chlorpheniramine.

Authors:  Hee-Kyung Hong; Su-Hyun Jo
Journal:  Korean J Physiol Pharmacol       Date:  2009-06-30       Impact factor: 2.016

5.  Clearance studies of methotrexate and 7-hydroxy-methotrexate in rabbits after multiple-dose infusion.

Authors:  M L Chen; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1983-10

6.  Pharmacokinetics of methotrexate and 7-hydroxy-methotrexate in rabbits after intravenous administration.

Authors:  M L Chen; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1983-10

7.  Pharmacokinetics of chlorpheniramine after intravenous and oral administration in normal adults.

Authors:  S M Huang; N K Athanikar; K Sridhar; Y C Huang; W L Chiou
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

8.  Oral absorption and presystemic first-pass effect of chlorpheniramine in rabbits.

Authors:  S M Huang; Y C Huang; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1981-12

9.  Long-Term Functional and Cytoarchitectonic Effects of the Systemic Administration of the Histamine H1 Receptor Antagonist/Inverse Agonist Chlorpheniramine During Gestation in the Rat Offspring Primary Motor Cortex.

Authors:  Rocío Valle-Bautista; Berenice Márquez-Valadez; Gabriel Herrera-López; Ernesto Griego; Emilio J Galván; Néstor-Fabián Díaz; José-Antonio Arias-Montaño; Anayansi Molina-Hernández
Journal:  Front Neurosci       Date:  2022-01-24       Impact factor: 4.677

  9 in total

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