UPLC-MS/MS determination of thiamphenicol in human plasma and its application to a pharmacokinetic study

被引:6
作者
Wang, Zhe [1 ,2 ]
Yang, Hui [3 ]
Sun, Wei [1 ,2 ]
Huang, Cheng-ke [1 ,2 ]
Cui, Xiao [1 ,2 ]
Qiu, Xiang-jun [3 ]
Lian, Qing-quan [2 ,4 ,5 ]
Wang, Zeng-shou [1 ,2 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Pharm, Wenzhou 325027, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Peoples R China
[3] Henan Univ Sci & Technol, Coll Med, Luoyang 471003, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 2, Zhejiang Prov Key Lab Anesthesiol, Wenzhou 325027, Peoples R China
[5] Wenzhou Med Univ, Affiliated Hosp 2, Dept Anesthesiol Crit Care & Pain Med, Wenzhou 325027, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2014年 / 967卷
关键词
Thiamphenicol; UPLC-MS/MS; Human plasma; Pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; FLORFENICOL AMINE; GAS-CHROMATOGRAPHY; CHLORAMPHENICOL; MICROEXTRACTION; HONEY; MUSCLE; RAT;
D O I
10.1016/j.jchromb.2014.07.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and rapid ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed to determine thiamphenicol (TAP) in human plasma using chlorzoxazone as the internal standard (IS). Sample preparation was accomplished through a liquid-liquid extraction procedure with ethyl acetate to precipitation of plasma protein, and to a 0.1 mL plasma sample. The analyte and IS were separated on an Acquity UPLC BEH C18 column (2.1 mm x 50 mm, 1.7 mu m) with the mobile phase of acetonitrile and I% formic acid in water with gradient elution at a flow rate of 0.40 mL/min. The detection was performed on a triple quadrupole tandem mass spectrometer equipped with electrospray ionization (ESI) by multiple reactions monitoring (MRM) of the transitions at m/z 354.3 -> 185.1 for TAP and m/z 168.1 -> 132.1 for IS. The linearity of this method was found to be within the concentration range of 10-8000 ng/mL with a lower limit of quantification of 10 ng/mL. Only 1.5 min was needed for an analytical run. The method herein described was superior to previous methods and was successfully applied to the pharmacokinetic study of TAP in healthy Chinese volunteers after oral administration. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 239
页数:5
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