Development and validation of a stereoselective liquid chromatography-tandem mass spectrometry assay for quantification of S- and R-metoprolol in human plasma

被引:42
作者
Jensen, Berit P. [1 ]
Sharp, Caroline F. [2 ]
Gardiner, Sharon J. [1 ]
Begg, Evan J. [1 ]
机构
[1] Univ Otago, Dept Med, Christchurch 8140, New Zealand
[2] Christchurch Hosp, Dept Pharm, Christchurch, New Zealand
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2008年 / 865卷 / 1-2期
关键词
metoprolol; enantiomers; LC-MS/MS; plasma;
D O I
10.1016/j.jchromb.2008.02.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A stereoselective liquid chromatography-tandem mass spectrometry assay was developed and validated for quantification of S- and R-metoprolol at concentrations of 0.5-50 mu g/L in human plasma. Metoprolol was extracted from plasma by liquid-liquid extraction with ethyl acetate (82% recovery). Chromatographic separation of the enantiomers was achieved on a chiral Chirobiotic T column using an isocratic mobile phase consisting of methanol/acetic acid/ammonia (100/0.15/0.15, v/v/v). An ion trap mass spectrometer with an electrospray interface was used for detection in the positive mode, monitoring the m/z transition 268 -> 191 for metoprolol. Standard curves for S- and R-metoprolol fitted quadratic functions (r(2) >= 0.9995) over the range 0.5-50 mu g/L in plasma, with 0.5 mu g/L representing the limit of quantification. In this range, relative standard deviations were <6% for intra-day precision and <10% for inter-day precision. The accuracy was within the range of 92-105%. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 54
页数:7
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