Intraindividual variability of paracetamol absorption kinetics after a semi-solid meal in healthy volunteers

被引:14
作者
Paintaud, G [1 ]
Thibault, P
Queneau, PE
Magnette, J
Bérard, M
Rumbach, L
Bechtel, PR
Carayon, P
机构
[1] Bretonneau Univ Hosp, Dept Pharmacol & Toxicol, F-37044 Tours, France
[2] Jean Minjoz Univ Hosp, Dept Clin Pharmacol, Besancon, France
[3] Jean Minjoz Univ Hosp, Dept Gastroenterol, Besancon, France
[4] Jean Minjoz Univ Hosp, Dept Neurol, Besancon, France
关键词
paracetamol; absorption;
D O I
10.1007/s002280050393
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The absorption kinetics of paracetamol is dependent on gastric emptying and its measurement was proposed as a non-invasive method to estimate gastric emptying rate. The objective of this study was to evaluate the intraindividual variability of paracetamol absorption kinetics after a semi-solid meal. Methods: The pharmacokinetics of paracetamol was studied on two occasions in 15 healthy volunteers without Helicobacter pylori antibodies. A 1-g dose of paracetamol was given as a solution together with a standardised semi-solid meal and the subjects stayed in the supine position. Results: For most of the subjects, the time course of paracetamol concentrations was similar on the two occasions. The intraindividual variability was low, with coefficients of variation of 38.3 %, 8.0 % and 3.8 % for time to maximum plasma concentration, maximum concentration and area under the plasma concentration - time curve until 6 h, respectively. Conclusion: The assessment of paracetamol absorption kinetics is reproducible when the drug is given together with a semi-solid meal in Helicobacter pylori-negative healthy subjects.
引用
收藏
页码:355 / 359
页数:5
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