Validated GC/MS method for the simultaneous determination of clozapine and norclozapine in human plasma. Application in psychiatric patients under clozapine treatment

被引:30
|
作者
Vardakou, I.
Dona, A.
Pistos, C. [1 ]
Alevisopoulos, G. [2 ]
Athanaselis, S.
Maravelias, C.
Spiliopoulou, C.
机构
[1] Univ Athens, Sch Med, Lab Forens Med & Toxicol, Dept Forens Med & Toxicol, GR-11527 Athens, Greece
[2] Univ Athens, Fac Nursing, Dept Psychiat & Behav Sci, GR-11527 Athens, Greece
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2010年 / 878卷 / 25期
关键词
Clozapine; Norclozapine; GC/MS; Plasma; Patients; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; N-DESMETHYLCLOZAPINE; QUANTITATIVE-DETERMINATION; HUMAN SERUM; METABOLITES; DRUGS; OLANZAPINE; BLOOD;
D O I
10.1016/j.jchromb.2010.07.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and specific GC/MS method for the determination of clozapine (CLZ) and its major metabolite norclozapine (NCLZ), in plasma has been developed, optimized and validated. Specimen preparation includes solid-phase extraction of both analytes using Bond-Elut Certify cartridge and further derivatization with TFAA. Clozapine-d8 was used as internal standard for the determination of CLZ and NCLZ. Limits of detection were 0.45 ng/mL for CLZ and 1.59 ng/mL for NCLZ, while limits of quantification were 1.37 ng/mL for CLZ and 4.8 ng/mL for NCLZ, as calculated by the calibration curves. The calibration curves were linear up to 600 ng/mL for CLZ and NCLZ. Absolute recovery ranged from 82.22% to 95.35% for both analytes. Intra- and interday accuracy was less than 7.13% and -12.52%, respectively, while intra- and interday precision was between 9.47% and 12.07%. respectively, for CLZ and NCLZ. The method covers all therapeutic range and proved suitable for the determination of CLZ and NCLZ not only in psychiatric patients but also in forensic cases with clozapine implication. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2327 / 2332
页数:6
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