The effect of acetaminophen administration on its disposition and body stores of sulphate
- 1 January 1986
- journal article
- research article
- Published by Springer Nature in European Journal of Clinical Pharmacology
- Vol. 30 (3) , 273-278
- https://doi.org/10.1007/bf00541527
Abstract
This investigation was designed to investigate the effects of ingestion of multiple therapeutic doses of acetaminophen on the disposition of the drug and on the cosubstrate, sulfate. Nine healthy volunteers and nine outpatients receiving acetaminophen for chronic pain were involved in the study. Volunteers were given a single 650 mg oral dose of acetaminophen. One week later they were given 650 mg of acetaminophen every six hours for five doses. Patients were maintained on their normal treatment and dosage schedules (600 mg every 3 to 8 h) for the study. In healthy volunteers the half-life of acetaminophen after single and multiple dosing was not significantly different. However, the fraction of acetaminophen recovered in the urine as the sulfate conjugate was less and the glucuronde conjugate greater after multiple dosing than after a single of the drug. There was no difference in the percentage recovered as the-parent compound between single and multiple dosing. Serum sulfate levels fluctuated over the 6-h period following administration of single and multiple doses of acetaminophen to volunteers. The mean serum sulfate concentration was less after administration of five sequential 650 mg doses of acetaminophen than after a single dose. The renal clearance of inorganic sulfate showed a corresponding decrease. Unexpectedly, patients on chronic acetaminophen therapy exhibited elevated serum sulfate levels (levels higher than the maximum sulfate concentration seen in volunteers).This publication has 19 references indexed in Scilit:
- The role of sulphate conjugation in the metabolism and disposition of oral and intravenous paracetamol in man.British Journal of Clinical Pharmacology, 1984
- Pharmacokinetic Consequences and Toxicologic Implications of Endogenous Cosubstrate DepletionDrug Metabolism Reviews, 1982
- Clinical Pharmacokinetics of ParacetamolClinical Pharmacokinetics, 1982
- High-performance liquid chromatographic determination of acetaminophen in plasma: single-dose pharmacokinetic studiesJournal of Chromatography B: Biomedical Sciences and Applications, 1981
- Absorption, serum levels and urinary excretion of inorganic sulfate after oral administration of sodium sulfate in the conscious ratBiochimica et Biophysica Acta (BBA) - General Subjects, 1979
- Paracetamol (Acetaminophen) Clearance in Patients with Cirrhosis of the LiverActa Medica Scandinavica, 1979
- Pharmacokinetics of paracetamol (acetaminophen) after intravenous and oral administrationEuropean Journal of Clinical Pharmacology, 1977
- Drug Biotransformation Interactions in Man III: Acetaminophen and SalicylamideJournal of Pharmaceutical Sciences, 1971
- A KINETIC STUDY OF DRUG ELIMINATION: THE EXCRETION OF PARACETAMOL AND ITS METABOLITES IN MANMETABOLITES IN MANBritish Journal of Pharmacology and Chemotherapy, 1967
- Turbidimetric Analysis of Inorganic Sulfate in Serum, Plasma and UrineScandinavian Journal of Clinical and Laboratory Investigation, 1960