Quantification of limonin in human urine using solid-phase extraction by LC-MS/MS

被引:16
作者
Liu, Shijia [1 ,2 ]
Zhang, Jun [2 ]
Zhou, Ling
Yu, Boyang [1 ]
Li, Changyin [2 ]
Liu, Zixiu
Ju, Wenzheng [2 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ Tradit Chinese Med, Affiliated Hosp, Nanjing 210009, Jiangsu, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2012年 / 907卷
关键词
Limonin; LC-MS/MS; SPE; Electrospray ionization; Human urine; IONIZATION MASS-SPECTROMETRY; CITRUS LIMONOIDS; CHROMATOGRAPHY; GLUCOSIDES; JUICES; HPLC;
D O I
10.1016/j.jchromb.2012.08.038
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitive liquid chromatography-tandem mass spectrometry method was developed and validated for the determination of limonin in human urine using podophyllotoxin as internal standard. The analyte and IS were extracted with solid-phase extraction and separated by a rapid isocratic elution with 1% formic acid/methanol (v:v, 40:60) on an C-18 column (150 mm x 2.1 mm ID.). The detection was performed by mass spectrometry in the multi-reaction-monitoring mode. The precursor to product ion transitions of m/z 471.3 -> 161.2 and m/z 397.2 -> 313.1 were used to measure the analyte and the IS. The assay was linear over the concentration range of 0.0783-10 ng/mL for limonin in human urine. The lower limit of quantification was 0.0783 ng/mL and the extraction recovery was larger than 76.7% for limonin. The inter- and intra-day precision of the method at three concentrations was less than 7.4%. The method was successfully applied to pharmacokinetic study of limonin in humans. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 167
页数:5
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