Determination of Tetrodotoxin in Human Urine and Plasma after Immunoaffinity Column Clean-up Using Ultra-Performanc Hydrophilic Interaction Chromatography Coupled with Triple Quadrupole Mass Spectrometry
10.11895/j.issn.0253-3820.140560
- VernacularTitle:免疫亲和柱净化-超高效亲水色谱-三重四极杆质谱联用法测定人尿液和血浆中河豚毒素
- Author:
Xiuyao ZHANG
;
Xinxin CAI
;
Xiaoyi ZHANG
;
Ruifen LI
- Publication Type:Journal Article
- Keywords:
Tetrodotoxin;
Immunoaffinity column clean-up;
Ultra-performance hydrophilic interaction liquid chromatography-tandem mass spectrometry;
Urine;
Plasma
- From:
Chinese Journal of Analytical Chemistry
2014;(11):1611-1616
- CountryChina
- Language:Chinese
-
Abstract:
Anultra-performancehydrophilicinteractionliquidchromatography-triplequadrupolemass spectrometric ( UPLC-MS/MS) method was developed for the determination of tetrodotoxin ( TTX) in human urine and plasma. After the sample was cleaned-up and concentrated by immunoaffinity column, the separation of the TTX was carried out on an Acquity UPLC BEH amide column (100 mm×2. 1 mm, 1. 7 μm) with gradient elution using mobile phases of 0. 1% ( V/V) formic acid in water and acetonitrile. The analyte was detected by positive electrospray ionization mass spectrometry in the multiple reaction monitoring ( MRM) mode, and quantified by external solvent standard calibration. The measuring ranges of TTX in urine and plasma were 0. 05-400 μg/L. The average recoveries were 92%-95% and 91%-96% for TTX respectively spiked in urine and plasma with relative standard deviations of 3 . 3%-7 . 2% and 3 . 9%-7 . 8% ( n=5 ) . The limits of detection (LOD, S/N=3) and limits of quantitation (LOQ, S/N=10) of TTX were 0. 02 μg/L and 0. 05μg/L for urine and plasma, respectively. This method is suitable for the detection of TTX in urine and plasma for both forensic and clinical purposes.
