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LC-MS/MS 法同时测定大鼠血浆中半枝莲提取物中 5 种黄酮类化合物的浓度及其药代动力学研究。

Simultaneous determination of five flavonoids from Scutellaria Barbata extract in rat plasma by LC-MS/MS and its application to pharmacokinetic study.

机构信息

School of Pharmacy, Hebei Medical University, Shijiazhuang, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jun 1;879(19):1625-32. doi: 10.1016/j.jchromb.2011.03.058. Epub 2011 Apr 8.

DOI:10.1016/j.jchromb.2011.03.058
PMID:21514902
Abstract

A new liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the determination of five flavonoids including scutellarin, naringenin, apigenin, luteoline and wogonin in rat plasma using sulfamethalazole as internal standard (IS). Plasma samples were pretreated with liquid-liquid extraction procedure and acid hydrolysis method was used for converting conjugated flavonoids to their respective free forms. The chromatographic separation was performed on a C(18) column with a linear gradient elution using a mobile phase consisted of 0.01% acetic acid and methanol. The detection was accomplished by multiple-reaction monitoring (MRM) scanning with electrospray ionization (ESI) source operating in the negative ionization mode. The optimized mass transition ion-pairs (m/z) monitored for scutellarin, naringenin, apigenin, luteoline, wogonin and IS were 461.1/285.1, 271.0/119.0, 269.0/117.0, 285.0/132.9, 283.0/268.0 and 252.0/155.9, respectively. The method was linear for all analytes over investigated ranges with all correlation coefficients greater than 0.9915. The lower limit of quantitation (LLOQ) of scutellarin was 9.15 ng/mL and other compounds were all less than 2.0 ng/mL. The proposed method showed appropriate accuracy and repeatability and was suitable for pharmacokinetic studies of the five flavonoids after oral administration of Scutellaria Barbata extract.

摘要

一种新的液相色谱-串联质谱(LC-MS/MS)方法已经被开发并验证,用于测定大鼠血浆中的五种黄酮类化合物,包括野黄芩苷、柚皮素、芹菜素、木犀草素和汉黄芩素,以磺胺甲恶唑为内标(IS)。血浆样品经过液-液萃取预处理,并用酸水解法将结合型黄酮类化合物转化为相应的游离形式。色谱分离在 C(18)柱上进行,采用含有 0.01%乙酸和甲醇的流动相进行线性梯度洗脱。检测采用电喷雾电离(ESI)源的多反应监测(MRM)扫描模式,在负离子模式下进行。优化的质量转移离子对(m/z)监测野黄芩苷、柚皮素、芹菜素、木犀草素、汉黄芩素和 IS 的分别为 461.1/285.1、271.0/119.0、269.0/117.0、285.0/132.9、283.0/268.0 和 252.0/155.9。该方法在研究范围内对所有分析物均呈线性,所有相关系数均大于 0.9915。野黄芩苷的定量下限(LLOQ)为 9.15ng/mL,其他化合物均小于 2.0ng/mL。该方法具有适当的准确性和重复性,适用于口服黄芩提取物后五种黄酮类化合物的药代动力学研究。

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