Development of SPME method for concomitant sample preparation of rocuronium bromide and tranexamic acid in plasma

被引:35
作者
Gorynski, Krzysztof [1 ,2 ]
Bojko, Barbara [1 ,2 ]
Kluger, Michael [3 ]
Jerath, Angela [3 ,4 ]
Wasowicz, Marcin [3 ,4 ]
Pawliszyn, Janusz [1 ]
机构
[1] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
[2] Nicolaus Copernicus Univ Torun, Coll Med Bydgoszcz, Dept Med Chem, PL-85089 Bydgoszcz, Poland
[3] Toronto Gen Hosp, Dept Anesthesia & Pain Management, Toronto, ON M5G 2C4, Canada
[4] Univ Toronto, Dept Anesthesia, Fac Med, Toronto, ON M5S 1A1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Weak cation exchange solid-phase microextraction (WCX-SPME); Liquid chromatography-mass spectrometry; Quaternary ammonium drug; Rocuronium bromide; Tranexamic acid; SOLID-PHASE MICROEXTRACTION; QUATERNARY AMMONIUM DRUGS; NEUROMUSCULAR BLOCKING-AGENTS; IONIZATION MASS-SPECTROMETRY; ELECTROSPRAY-IONIZATION; PHARMACODYNAMIC RELATIONSHIP; EQUINE URINE; WHOLE-BLOOD; PHARMACOKINETICS; METABOLITES;
D O I
10.1016/j.jpba.2014.01.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A high-throughput method using solid-phase microextraction coupled to liquid chromatography-tandem mass spectrometry (SPME-LC-MS/MS) for determination of tranexamic acid and rocuronium bromide in human plasma was developed and validated. Standard analytical approaches employ acidification of the sample due to the instability of rocuronium bromide in collected plasma samples. However, acidification affects the binding equilibrium of the drug and consequently no information on the free/bound concentration can be obtained. Contrary to these protocols, the proposed method requires minimum sample handling and no ion pairing and/or derivatization procedure. A weak cation exchange coating was chosen as the best extracting phase for selected drugs, guaranteed a good recovery, minimum carry-over, reusability and reproducibility. SPME procedure met all Food and Drug Administration acceptance criteria for bioanalytical assays at three concentration levels, for both selected drugs. Post-extraction addition experiments showed that matrix effect was less than +/- 3%. Here, a weak cation exchange thin-film solid-phase microextraction (WCX TF-SPME) approach is presented, offering effective cleanup procedure and full quantitation of the drugs in plasma, undoubtedly one the most challenging matrices with regards to its complexity. In addition, the 96-well plate format of WCX TF-SPME system provides considerable advantages, such as high throughput analysis for up to 96 samples in 35 min (22 s/sample), requirement of small amounts of plasma samples (0.8 mL), and a simple sample preparation protocol, all of which shows a promise for possible on-site application in hospitals to monitor concentrations of the drugs in close to real time. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 192
页数:10
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