Literature DB >> 2257860

Paracetamol test: modification by renal function, urine flow and pH.

D Kietzmann1, K W Bock, B Krähmer, D Kettler, J Bircher.   

Abstract

Factors which might affect paracetamol disposition have been studied in a heterogenous group of patients in need of mild analgesia in an intensive care unit. Following oral administration of 1 g of paracetamol, plasma and urinary concentrations of the parent compound and metabolites were assessed by HPLC. The renal clearance of paracetamol was significantly correlated with urine flow (r = 0.84) and creatinine clearance (r = 0.77), but not with urine pH. Metabolite output was diminished in patients with reduced renal function. Despite the heterogeneity of patients and the diversity of drug treatment, the urine to plasma paracetamol concentration ratio appeared remarkably constant in patients with normal renal function (9.8 +/- 2.7). It is concluded that the metabolite to paracetamol ratio may only be regarded as a measure of the drug metabolizing capacity in subjects with normal renal function, if factors influencing urine volume and paracetamol absorption are standardized.

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Year:  1990        PMID: 2257860     DOI: 10.1007/bf00315104

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  12 in total

1.  Paracetamol metabolism following overdosage: application of high performance liquid chromatography.

Authors:  D Howie; P I Adriaenssens; L F Prescott
Journal:  J Pharm Pharmacol       Date:  1977-04       Impact factor: 3.765

2.  The dependence of paracetamol absorption on the rate of gastric emptying.

Authors:  R C Heading; J Nimmo; L F Prescott; P Tothill
Journal:  Br J Pharmacol       Date:  1973-02       Impact factor: 8.739

3.  Absolute bioavailability of paracetamol after oral or rectal administration in healthy volunteers.

Authors:  M Eandi; I Viano; S Ricci Gamalero
Journal:  Arzneimittelforschung       Date:  1984

4.  The binding of paracetamol to plasma proteins of man and pig.

Authors:  B G Gazzard; A W Ford-Hutchinson; M J Smith; R Williams
Journal:  J Pharm Pharmacol       Date:  1973-12       Impact factor: 3.765

5.  Paracetamol metabolism and toxicity in isolated hepatocytes from rat and mouse.

Authors:  P Moldéus
Journal:  Biochem Pharmacol       Date:  1978       Impact factor: 5.858

6.  A kinetic study of drug elimination: the excretion of paracetamol and its metabolites in man.

Authors:  A J Cummings; M L King; B K Martin
Journal:  Br J Pharmacol Chemother       Date:  1967-02

7.  Pharmacokinetics of acetaminophen elimination by anephric patients.

Authors:  D T Lowenthal; S Oie; J C Van Stone; W A Briggs; G Levy
Journal:  J Pharmacol Exp Ther       Date:  1976-03       Impact factor: 4.030

8.  Paracetamol as a test drug to determine glucuronide formation in man. Effects of inducers and of smoking.

Authors:  K W Bock; J Wiltfang; R Blume; D Ullrich; J Bircher
Journal:  Eur J Clin Pharmacol       Date:  1987       Impact factor: 2.953

9.  Drug interactions: inhibition of acetaminophen glucuronidation by drugs.

Authors:  W Bolanowska; T Gessner
Journal:  J Pharmacol Exp Ther       Date:  1978-07       Impact factor: 4.030

Review 10.  Kinetics and metabolism of paracetamol and phenacetin.

Authors:  L F Prescott
Journal:  Br J Clin Pharmacol       Date:  1980-10       Impact factor: 4.335

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  2 in total

1.  Perturbation of paracetamol urinary metabolic ratios by urine flow rate.

Authors:  J O Miners; N J Osborne; A L Tonkin; D J Birkett
Journal:  Br J Clin Pharmacol       Date:  1992-10       Impact factor: 4.335

2.  The biochemistry of acetaminophen hepatotoxicity and rescue: a mathematical model.

Authors:  Rotem Ben-Shachar; Yifei Chen; Shishi Luo; Catherine Hartman; Michael Reed; H Frederik Nijhout
Journal:  Theor Biol Med Model       Date:  2012-12-19       Impact factor: 2.432

  2 in total

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