Determination of sec-O-glucosylhamaudol in rat plasma by gradient elution liquid chromatography-mass spectrometry

被引:56
作者
Wen, Congcong [1 ]
Lin, Chongliang [2 ]
Cai, Xiaojun [3 ]
Ma, Jianshe [3 ]
Wang, Xianqin [3 ]
机构
[1] Wenzhou Med Univ, Lab Anim Ctr, Wenzhou 325035, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Wenzhou 325000, Peoples R China
[3] Wenzhou Med Univ, Analyt & Testing Ctr, Wenzhou 325035, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2014年 / 944卷
关键词
Sec-O-glucosylhamaudol; LC-MS; Pharmacokinetics; Rat plasma; RADIX SAPOSHNIKOVIAE; 4; CHROMONES; COMPONENTS; DIVARICATA; EXTRACTION;
D O I
10.1016/j.jchromb.2013.11.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sec-O-glucosylhamaudol is one of the major bioactive compounds of the Saposhnikoviae Radix. A simple and selective liquid chromatography-mass spectrometry (LC-MS) method for determination of sec-O-glucosylhamaudol in rat plasma was developed. After addition of carbamazepine as internal standard (IS), protein precipitation with acetonitrile-methanol (9:1, v/v) was used as sample preparation. Chromatographic separation was achieved on a Zorbax SB-C18 (2.1 mm x 150 mm, 5 mu m) column with acetonitrile-0.1% formic acid in water as mobile phase with gradient elution. Electrospray ionization (ESI) source was applied and operated in positive ion mode; selective ion monitoring (SIM) mode was used for quantification using target fragment ions m/z 439 for sec-O-glucosylhamaudol and m/z 237 for the IS. Calibration plots were linear over the range of 50-8000 ng/mL for sec-O-glucosylhamaudol in rat plasma. Mean recovery of sec-O-glucosylhamaudol in plasma was in the range of 74.8-83.7%. Intra-day and inter-day precision were both <15%. This method was successfully applied in pharmacokinetic study after intravenous administration of 2.5 mg/kg sec-O-glucosylhamaudol in rats. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:35 / 38
页数:4
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