PHARMACOKINETICS OF SULPIRIDE IN HUMANS AFTER INTRAVENOUS AND INTRAMUSCULAR ADMINISTRATIONS

被引:17
作者
BRES, J
BRESSOLLE, F
机构
[1] Laboratoire de Pharmacocinétique, Faculté de Pharmacie, Université de Montpellier I, Montpellier, 34060
关键词
D O I
10.1002/jps.2600801206
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
The pharmacokinetics of sulpiride in plasma, red blood cells (RBC), and urine were investigated after administration of 100 mg by the iv route to 15 subjects and by the im route to 12 subjects. The concentrations of sulpiride in plasma, RBC, and urine were measured by HPLC. All the data were consistent with a two-compartment, open-body model. After iv administration, the mean +/- SD apparent elimination half-life of sulpiride was 6.47 +/- 1.00 h, and the mean +/- SD volume of distribution at steady state was 0.94 +/- 0.23 L/kg. Renal clearance (119.5 +/- 28.2 mL/min) was very close to total clearance (127.8 +/- 26.2 mL/min). In urine, the mean +/- SD recovery in form of the unchanged drug was 90.0 +/- 9.68% of the administered dose, and the excretion rate versus time showed an elimination half-life similar to that found in plasma. The values of all these parameters were very close to those obtained after im administration. The sulpiride partition coefficient between RBC and plasma did not show any significant change as a function of time and concentration, with a mean value +/- SD of 1.00 +/- 0.043, indicating that sulpiride is evenly distributed between RBC and plasma. The pharmacokinetic parameters determined from the plasma and the RBC data were similar.
引用
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页码:1119 / 1124
页数:6
相关论文
共 27 条
[1]
ALAM AS, 1979, ARCH INT PHARMACOD T, V242, P4
[2]
RELATIONSHIPS BETWEEN DRUG CONCENTRATIONS IN SERUM AND CSF, CLINICAL EFFECTS AND MONOAMINERGIC VARIABLES IN SCHIZOPHRENIC-PATIENTS TREATED WITH SULPIRIDE OR CHLORPROMAZINE [J].
ALFREDSSON, G ;
BJERKENSTEDT, L ;
EDMAN, G ;
HARNRYD, C ;
OXENSTIERNA, G ;
SEDVALL, G ;
WIESEL, FA .
ACTA PSYCHIATRICA SCANDINAVICA, 1984, 69 :49-74
[3]
PLASMA AND INTRACELLULAR KINETICS OF LITHIUM AFTER ORAL-ADMINISTRATION OF VARIOUS LITHIUM-SALTS [J].
ALTAMURA, AC ;
GOMENI, R ;
SACCHETTI, E ;
SMERALDI, E .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1977, 12 (01) :59-63
[4]
BRES J, 1985, THERAPIE, V40, P433
[5]
BRES J, 1979, C HISPANO FRANCAIS B, V3, P25
[6]
SULPIRIDE PHARMACOKINETICS IN HUMANS AFTER INTRAMUSCULAR ADMINISTRATION AT 3 DOSE LEVELS [J].
BRESSOLLE, F ;
BRES, J ;
BLANCHIN, MD ;
GOMENI, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (08) :1128-1136
[7]
QUANTITATIVE-ANALYSIS OF SULPIRIDE AND SULTOPRIDE BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY FOR PHARMACOKINETIC STUDIES [J].
BRESSOLLE, F ;
BRES, J .
JOURNAL OF CHROMATOGRAPHY, 1985, 341 (02) :391-399
[8]
PHARMACOKINETICS OF SULPIRIDE AFTER INTRAVENOUS ADMINISTRATION IN PATIENTS WITH IMPAIRED RENAL-FUNCTION [J].
BRESSOLLE, F ;
BRES, J ;
MOURAD, G .
CLINICAL PHARMACOKINETICS, 1989, 17 (05) :367-373
[9]
BRESSOLLE F, 1986, BIOACTIVE ANAL INCLU, V16, P189
[10]
BRESSOLLE F, 1984, 2ND EUR C BIOPH PHAR, V3, P287