Quantification of zolmitriptan in plasma by high-performance liquid chromatography-electrospray ionization mass spectrometry

被引:23
|
作者
Zhang, ZJ [1 ]
Xu, FG
Tian, Y
Li, W
Mao, GG
机构
[1] China Pharmaceut Univ, Ctr Instrumental Anal, Nanjing 210009, Peoples R China
[2] Wannan Med Coll, Dept Clin Pharmacol, Wuhu 241000, Peoples R China
关键词
zolmitriptan; HPLC-ESI-MS; human plasma; pharmacokinetics;
D O I
10.1016/j.jchromb.2004.09.043
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and specific liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS) method has been developed and validated for the identification and quantification of zolmitriptan in human plasma. After the addition of the internal standard (IS) and 1.0 M sodium hydroxide solution, plasma samples were extracted with methylene chloride:ethyl acetate mixture (20:80, v/v). The organic layer was evaporated under a stream of nitrogen at 40degreesC. The residue was reconstituted with 100 RI mobile phase. The compounds were separated on a prepacked Lichrospher CN (5 mum, 150 mm x 2.0 mm) column using a mixture of methanol:water (10 mM NH(4)AC, pH 4.0) = 78:22 as mobile phase. Detection was performed on a single quadrupole mass spectrometer by selected ion monitoring (SIM) mode via electrospray ionization (ESI) source. The method was proved to be sensitive and specific by testing six different plasma batches. Linearity was established for the range of concentrations 0.30-16.0 ng/mI with a coefficient of determination (r) of 0.9998 and good back-calculated accuracy and precision. The intra- and inter-day precision (R.S.D.%) were lower than 15% and accuracy ranged from 85 to 115%. The lower limit of quantification was identifiable and reproducible at 0.30 ng/ml. The proposed method enables the unambiguous identification and quantification of zolmitriptan for pharmacokinetic, bioavailability or bioequivalence studies. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:227 / 233
页数:7
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