Planta Med 2013; 79(01): 30-36
DOI: 10.1055/s-0032-1327983
Pharmacokinetic Investigations
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Determination of Cnidilin and Its Two Metabolites in Rat Plasma by High-performance Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry

Hong Zhu
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
2   Department of Pharmacy, 302 Hospital of Peopleʼs Liveration Army LA, Beijing, China
,
Pengwei Liu
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
,
Xiaowei Shi
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
,
Huijun Xu
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
,
Yanping Ren
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
,
Qiao Wang
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
,
Lantong Zhang
1   Department of Pharmaceutical Analysis, School of Pharmacy Hebei Medical University, Shijiazhuang, China
› Author Affiliations
Further Information

Publication History

received 25 July 2012
revised 14 October 2012

accepted 21 October 2012

Publication Date:
27 November 2012 (online)

Abstract

Simple, fast, and sensitive HPLC coupled with an electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS) method for the simultaneous determination of cnidilin and its two metabolites, 3″,8-methoxy-isoimperatorin (M1) and 5″-hydroxyl-8-methoxy-isoimperatorin (M2), in rat plasma has been developed. Pimpinellin was used as the internal standard and the total analysis time was 7 min. Methanol was the only reagent during the process of sample handling used as a protein precipitant. The analytes were separated on a reversed-phase C18 column with gradient elution consisting of 0.5 ‰ aqueous formic acid and methanol (containing 0.5 ‰ formic acid) in the multiple-reaction monitoring mode. Cnidilin, M1, M2, and the internal standard could be well ionized under positive electrospray ionization conditions. Full validation of the method (linearity, precision, accuracy, limit of detection, and limit of quantification) was carried out and the method was successfully employed in a metabolism study of cnidilin administered to rats at a dose of 24 mg/kg. The pharmacokinetic parameters of cnidilin determined after orally administrating the single coumarin to the rat were obtained and the mass fragmentation pathways for analysis are proposed in this article.

 
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