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http://dx.doi.org/10.5012/bkcs.2013.34.6.1684

Liquid Chromatography Quadrupole Time-Of-Flight Tandem Mass Spectrometry for Selective Determination of Usnic Acid and Application in Pharmacokinetic Study  

Fang, Minfeng (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Wang, Hui (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Wu, Yang (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Wang, Qilin (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Zhao, Xinfeng (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Zheng, Xiaohui (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Wang, Shixiang (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Zhao, Guifang (Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Northwest University)
Publication Information
Abstract
A rapid and sensitive method for determining usnic acid of Lethariella cladonioides in rat was established using high performance liquid chromatography (HPLC) quadrupole time-of-flight (QTOF) tandem mass (MS/MS). Rat plasma was pretreated by mixture of acetonitrile and chloroform to precipitate plasma proteins. Chromatographic separation was achieved on a column ($50{\times}2.1$ mm, $5{\mu}m$) with a mobile phase consisting of water (containing $5{\times}10^{-3}$ M ammonium formate, pH was adjusted to 3.0 with formic acid) and acetonitrile (20:80, v/v) at a flow rate of 0.3 mL/min. A tandem mass spectrometric detection with an electrospray ionization (ESI) interface was conducted via collision induced dissociation (CID) under negative ionization mode. The MS/MS transitions monitored were m/z 343.0448 ${\rightarrow}$ m/z 313.2017 for usnic acid and m/z 153.1024 ${\rightarrow}$ m/z 136.2136 for protocatechuic acid (internal standard). The linear range was calculated to be 2.0-160.0 ng/mL with a detection limit of 3.0 pg/mL. The inter- and intra-day accuracy and precision were within ${\pm}7.0%$. Pharmacokinetic study showed that the apartment of usnic acid in vivo confirmed to be a two compartment open model. The method was fully valid and will probably be an alternative for pharmacokinetic study of usnic acid.
Keywords
Liquid chromatography; Time of flight; Mass spectrometry; Usnic acid;
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