DEVELOPMENT AND PRELIMINARY APPLICATION OF HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ASSAY OF URINARY METABOLITES OF DIAZEPAM IN HUMANS

被引:26
作者
CHIBA, K
HORII, H
CHIBA, T
KATO, Y
HIRANO, T
ISHIZAKI, T
机构
[1] SCI UNIV TOKYO,DEPT PHARMACEUT SCI,SHINJUKU KU,TOKYO 162,JAPAN
[2] HIROSAKI UNIV,SCH MED,DEPT NEUROPSYCHIAT,HIROSAKI,AOMORI 036,JAPAN
来源
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS | 1995年 / 668卷 / 01期
关键词
D O I
10.1016/0378-4347(95)00050-S
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple high-performance liquid chromatographic method for the measurement of diazepam (DZP) and its major metabolites, N-desmethyldiazepam (DMDZP), temazepam (TZP) and oxazepam (OZP) in urine was developed. Preliminary studies of DZP metabolism were also undertaken in four healthy volunteers after administration of a single oral dose (4 mg) of DZP. The assay allowed the simultaneous determination of all analytes in 1 ml of urine and the detection limit was 2 ng/ml with a signal-to-noise ratio of 3. None of 22 drugs and 17 metabolites, except for mianserin, maprotiline and imipramine N-oxide, interfered with the detection of DZP metabolites. Recoveries of the analytes and the internal standard (prazepam) were >82%. Intra- and inter-assay coefficients of variation for all analytes were <5.5 and 4.1%, respectively. The mean (+/- S.D.) cumulative urinary excretions of DMDZP, TZP and OZP over 96 h after a single oral administration of DZP were 3.9 +/- 0.4, 6.6 +/- 1.4 and 2.8 +/- 0.6% of the dose, respectively. The urinary excretion of DZP was under the detection limit.
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页码:77 / 84
页数:8
相关论文
共 20 条
[1]   DIAZEPAM METABOLISM BY HUMAN LIVER-MICROSOMES IS MEDIATED BY BOTH S-MEPHENYTOIN HYDROXYLASE AND CYP3A ISOFORMS [J].
ANDERSSON, T ;
MINERS, JO ;
VERONESE, ME ;
BIRKETT, DJ .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1994, 38 (02) :131-137
[2]  
ARNOLD E, 1975, ACTA PHARMACOL TOX, V36, P335
[3]   IMPORTANCE OF GENETIC-FACTORS IN THE REGULATION OF DIAZEPAM METABOLISM - RELATIONSHIP TO S-MEPHENYTOIN, BUT NOT DEBRISOQUIN, HYDROXYLATION PHENOTYPE [J].
BERTILSSON, L ;
HENTHORN, TK ;
SANZ, E ;
TYBRING, G ;
SAWE, J ;
VILLEN, T .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1989, 45 (04) :348-355
[4]   DETERMINATION OF DIAZEPAM AND ITS MAJOR METABOLITES IN MAN AND IN THE CAT BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COTLER, S ;
PUGLISI, CV ;
GUSTAFSON, JH .
JOURNAL OF CHROMATOGRAPHY, 1981, 222 (01) :95-106
[5]   DETERMINATION OF DIAZEPAM ( VALIUM ) IN BLOOD BY GAS LIQUID CHROMATOGRAPHY [J].
DESILVA, JAF ;
SCHWARTZ, MA ;
KAPLAN, J ;
STEFANOVIC, V ;
DARCONTE, L .
ANALYTICAL CHEMISTRY, 1964, 36 (11) :2099-&
[6]   DIAZEPAM DISPOSITION DETERMINANTS [J].
GREENBLATT, DJ ;
ALLEN, MD ;
HARMATZ, JS ;
SHADER, RI .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1980, 27 (03) :301-312
[7]  
GREENBLATT DJ, 1983, NEW ENGL J MED, V309, P354
[8]  
GREENBLATT DJ, 1983, NEW ENGL J MED, V309, P410
[9]   BENZODIAZEPINE KINETICS - IMPLICATIONS FOR THERAPEUTICS AND PHARMACOGERIATRICS [J].
GREENBLATT, DJ ;
DIVOLL, M ;
ABERNETHY, DR ;
OCHS, HR ;
SHADER, RI .
DRUG METABOLISM REVIEWS, 1983, 14 (02) :251-292
[10]  
KANTO J, 1978, INT J CLIN PHARM BI, V16, P258