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采用高效液相色谱-电喷雾电离质谱法对血浆中佐米曲普坦进行定量分析。

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

作者信息

Zhang Zunjian, Xu Fengguo, Tian Yuan, Li Wei, Mao Guoguang

机构信息

Center for Instrumental Analysis, China Pharmaceutical University, Nanjing 210009, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Dec 25;813(1-2):227-33. doi: 10.1016/j.jchromb.2004.09.043.

Abstract

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 40 degrees C. The residue was reconstituted with 100 microl mobile phase. The compounds were separated on a prepacked Lichrospher CN (5 microm, 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/ml 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.

摘要

已开发并验证了一种灵敏且特异的液相色谱-电喷雾电离质谱法(LC-ESI-MS),用于人血浆中佐米曲普坦的鉴定和定量。加入内标(IS)和1.0 M氢氧化钠溶液后,血浆样品用二氯甲烷:乙酸乙酯混合物(20:80,v/v)萃取。有机层在40℃氮气流下蒸发。残留物用100微升流动相复溶。化合物在预填充的Lichrospher CN(5微米,150毫米×2.0毫米)柱上分离,以甲醇:水(10 mM NH4AC,pH 4.0)=78:22的混合物作为流动相。通过电喷雾电离(ESI)源,在单四极杆质谱仪上采用选择离子监测(SIM)模式进行检测。通过测试六个不同的血浆批次,证明该方法灵敏且特异。在0.30-16.0 ng/ml浓度范围内建立了线性关系,测定系数(r)为0.9998,回算精度和精密度良好。日内和日间精密度(R.S.D.%)低于15%,准确度在85%至115%之间。定量下限在0.30 ng/ml时可识别且可重现。所提出的方法能够明确鉴定和定量佐米曲普坦,用于药代动力学、生物利用度或生物等效性研究。

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