Liquid chromatographic-mass spectrometric determination of haloperidol and its metabolites in human plasma and urine

被引:38
作者
Arinobu, T [1 ]
Hattori, H
Iwai, M
Ishii, A
Kumazawa, T
Suzuki, O
Seno, H
机构
[1] Aichi Med Univ, Sch Med, Dept Legal Med, Nagakute, Aichi 4801195, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Legal Med & Bioeth, Showa Ku, Nagoya, Aichi 4648550, Japan
[3] Showa Univ, Sch Med, Dept Legal Med, Shinagawa Ku, Tokyo 1428555, Japan
[4] Hamamatsu Univ Sch Med, Dept Legal Med, Hamamatsu, Shizuoka 4313192, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2002年 / 776卷 / 01期
关键词
haloperidol;
D O I
10.1016/S1570-0232(02)00175-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Haloperidol and its two metabolites, reduced haloperidol and 4-(4-chlorophenyl)-4-hydroxypiperidine (CPHP) in human plasma and urine were analyzed by HPLC-MS using a new polymer column (MSpak GF-310), which enabled direct injection of crude biological samples without pretreatment. Recoveries of haloperidol and reduced haloperidol spiked into plasma were 64.4-76.1% and 46.8-50.2%, respectively; those for urine were 87.3-99.4% and 94.2-98.5%, respectively; those of CPHP for both samples were not less than 92.7%. The regression equations for haloperidol, reduced haloperidol and CPHP showed good linearity in the ranges of 10-800, 15-800 and 400-800 ng/ml, respectively, for both plasma and urine. Their detection limits were 5, 10 and 300 ng/ml, respectively, for both samples. Thus, the present method was sensitive enough for detection and determination of high therapeutic and toxic levels for haloperidol and its metabolites present in biological samples. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 113
页数:7
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