Simultaneous determination of 6 beta-blockers, 3 calcium-channel antagonists, 4 angiotensin-II antagonists and 1 antiarrhytmic drug in post-mortem whole blood by automated solid phase extraction and liquid chromatography mass spectrometry - Method development and robustness testing by experimental design

被引:130
作者
Kristoffersen, Lena
Oiestad, Elisabeth Leere
Opdal, Mimi Stokke
Krogh, Mette
Lundanes, Elsa
Christophersen, Asbjorg Solberg
机构
[1] Norwegian Inst Publ Hlth, Div Forens Toxicol & Drug Abuse, N-0403 Oslo, Norway
[2] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 850卷 / 1-2期
关键词
cardiovascular drugs; beta-blockers; calcium-channel antagonists; angiotensin-II antagonists; antiarrythmic drug; whole blood; experimental design; SPE; HPLC-MS;
D O I
10.1016/j.jchromb.2006.11.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for the simultaneous determination of the beta-blockers atenolol, sotalol, metoprolol, bisoprolol, propranolol and carvedilol, the calcium-channel antagonists diltiazem, amlodipine and verapamil, the angiotensin-II antagonists losartan, irbesartan, valsartan and telmisartan, and the antiarrythmic drug flecainide, in whole blood samples from forensic autopsies was developed. Sample clean-up was achieved by precipitation and solid phase extraction (SPE) with a mixed-mode column. Quantification was performed by reversed phase high performance liquid chromatography with positive electrospray ionization mass spectrometric detection (HPLC-MS). The method has been developed and robustness tested by systematically searching for satisfactory conditions using experimental designs including factorial and response surface designs. With the exception of amlodipine, the concentration limit of quantification (cLOQ) covered low therapeutic concentration levels for all the compounds. Within assay precisions and accuracies (bias) were 3.4-21 % RSD and from -24 to 21 % for the concentration range 1.00-5.00 mu M, respectively. Between assay precisions were 4.4-28% RSD for the concentration range from 0. 1 to 5 mu M and recoveries varied from 9 to 103%. The method is used for determination of cardiovascular drugs in post-mortem whole blood samples from forensic autopsy cases. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 160
页数:14
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