Sensitive liquid chromatographic mass spectrometric assay for the simultaneous quantitation of nefazodone and its metabolites hydroxynefazodone m-chlorophenylpiperazine and triazole-dione in human plasma using single-ion monitoring

被引:16
作者
Yao, M [1 ]
Shah, VR [1 ]
Shyu, WC [1 ]
Srinivas, NR [1 ]
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Dept Metab & Pharmacokinet, Princeton, NJ 08543 USA
来源
JOURNAL OF CHROMATOGRAPHY B | 1998年 / 718卷 / 01期
关键词
nefazodone; hydroxynefazodone; m-chlorophenylpiperazine; triazole-dione;
D O I
10.1016/S0378-4347(98)00355-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive, selective, accurate, precise and reproducible high-performance liquid chromatographic-mass spectrometric (LC-MS) assay was developed and validated for the simultaneous determination of nefazodone (NEF), hydroxynefazodone (OH-NEF), m-chlorophenylpiperazine (mCPP), and triazole-dione (Dione) in human plasma using trazodone (TRZ) as the internal standard (LS.). The method involved simultaneous protein precipitation with acetonitrile and liquid-liquid extraction with methylene chloride, after which the organic layer was evaporated to dryness. The residue was reconstituted in 25% acetonitrile in 10 mM ammonium formate (pH 4.0), and an aliquot was injected onto a BDS Hypersil C-18 column at a flow-rate of 0.3 ml/min. The mobile phase comprising of 10 mM ammonium formate (pH 4) and acetonitrile in 55:45 (v/v) was used in an isocratic condition. The mass spectrometer was programmed to admit the protonated molecules at m/z 197.0 (mCPP), 372.0 (I.S.) 470.4 (NEF), 458.1 (Dione), and 486.2 (OH-NEF). Standard curves were Linear (r(2)greater than or equal to 0.995) over the concentration range of 4-2000 ng/ml for Dione and 2-500 ng/ml for other analytes. The lowest standard concentrations were the lower limit of quantitation for each analyte. The mean predicted quality control (QC) concentrations for all analytes deviated less than -12.1% from the corresponding nominal values; the intra-assay and inter-assay precision of the assay for all analytes were within 7.0% relative standard deviation. All analytes including I.S. were stable in the injection solvent at room temperature for at least 24 h. The extraction recovery of the various analytes ranged from 67.3 to 86.5%. The validated assay was applied to a pharmacokinetic study of nefazodone. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:77 / 85
页数:9
相关论文
共 6 条
[1]  
EISON AS, 1989, PSYCHOPHARMACOL B, V25, P219
[2]  
FEIGHNER JP, 1989, PSYCHOPHARMACOL BULL, V25, P219
[3]   HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHOD FOR THE DETERMINATION OF NEFAZODONE AND ITS METABOLITES IN HUMAN PLASMA USING LABORATORY ROBOTICS [J].
FRANC, JE ;
DUNCAN, GF ;
FARMEN, RH ;
PITTMAN, KA .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1991, 570 (01) :129-138
[4]   DETERMINATION OF NEFAZODONE AND ITS METABOLITES IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH COULOMETRIC DETECTION [J].
FRANKLIN, M .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1993, 11 (11-12) :1109-1113
[5]   TRIAZOLO ANTIDEPRESSANTS DO NOT INHIBIT MONOAMINE-OXIDASE [J].
HYSLOP, DK ;
ALLEN, LE ;
TAYLOR, DP .
DRUG DEVELOPMENT RESEARCH, 1988, 12 (01) :77-79
[6]  
MAYOL RF, 1994, DRUG METAB DISPOS, V22, P304