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采用液相色谱-电喷雾电离质谱法同时灵敏测定大鼠血浆中的补骨脂素、花椒毒素、异茴芹素和佛手柑内酯。

Simultaneous and sensitive determination of xanthotoxin, psoralen, isoimpinellin and bergapten in rat plasma by liquid chromatography-electrospray ionization mass spectrometry.

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Hebei Medical University, 361 Zhongshan East Road, Shijiazhuang 050017, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Feb 15;878(5-6):575-82. doi: 10.1016/j.jchromb.2009.12.035. Epub 2010 Jan 14.

Abstract

A sensitive, specific and rapid liquid chromatography-mass spectrometry (LC-MS) method has been developed and validated for the simultaneous determination of xanthotoxin (8-methoxypsoralen), psoralen, isoimpinellin (5,8-dimethoxypsoralen) and bergapten (5-methoxypsoralen) in rat plasma using pimpinellin as an internal standard (IS). The plasma samples were pretreated by protein precipitation with methanol and chromatographic separation was performed on a C(18) column with a mobile phase composed of 1 mmol ammonium acetate and methanol (30:70, v/v). The detection was accomplished by multiple-reaction monitoring (MRM) scanning via electrospray ionization (ESI) source operating in the positive ionization mode. The optimized mass transition ion-pairs (m/z) for quantitation were 217.1/202.1 for xanthotoxin, 187.1/131.1 for psoralen, 247.1/217.0 for isoimpinellin, 217.1/202.1 for bergapten, and 247.1/231.1 for IS. The total run time was 6 min between injections. The calibration curves were linear over the investigated concentration range with all correlation coefficients higher than 0.998. The lower limits of quantitation (LLOQ) of these analytes were less than 1.21 ng/ml. The intra- and inter-day RSD were no more than 9.7% and the relative errors were within the range of -8.1% to 4.5%. The average extraction recoveries for all compounds were between 90.7% and 106.2%. The proposed method was further applied to the determination of actual plasma samples from rats after oral administration of Radix Glehniae extract.

摘要

建立并验证了一种灵敏、特异、快速的液相色谱-质谱(LC-MS)法,用于同时测定大鼠血浆中西当归素(8-甲氧基补骨脂素)、补骨脂素、异茴芹素(5,8-二甲氧基补骨脂素)和花椒毒素(5-甲氧基补骨脂素),以茴芹素为内标(IS)。采用甲醇沉淀蛋白法预处理血浆样品,以 1mmol 乙酸铵和甲醇(30:70,v/v)为流动相,在 C(18)柱上进行色谱分离。采用电喷雾电离(ESI)源,正离子模式下进行多反应监测(MRM)扫描进行检测。定量分析的优化质量转换离子对(m/z)分别为 217.1/202.1 用于测定花椒毒素,187.1/131.1 用于测定补骨脂素,247.1/217.0 用于测定异茴芹素,217.1/202.1 用于测定花椒毒素,247.1/231.1 用于测定 IS。两次进样之间的总运行时间为 6 分钟。在考察的浓度范围内,校准曲线均呈线性,相关系数均大于 0.998。这些分析物的定量下限(LLOQ)均小于 1.21ng/ml。日内和日间 RSD 均不超过 9.7%,相对误差在-8.1%至 4.5%范围内。所有化合物的平均提取回收率在 90.7%至 106.2%之间。该方法进一步应用于大鼠口服甘白芷提取物后实际血浆样品的测定。

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