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| Simultaneous Determination of Amantadine and Rimantadine Residues in Swine Urine by LC-MS/MS |
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| DOI：10.3969/j.issn.1004-4957.年份.月份 |
| KeyWord:ultra performance liquid chromatography-electrospray tandem mass spectrometry（UPLC-ESI-MS/MS） amantadine rimantadine swine urine |
| Author | Institution |
| HU Li-fang，ZHANG Jin-yan，LUO Lin-guang* |
江西省农业科学院农产品质量安全与标准研究所农产品质量安全重点实验室 |
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| Abstract: |
| A rapid determination method for amantadine and rimantadine in swine urine was established using ultra performance liquid chromatography-electrospray tandem mass spectrometry（UPLC-ESI-MS/MS） in multiple reaction monitoring（MRM） mode.The urine sample was extracted with acetonitrile by ultrasonic,and cleaned up with solid-phase extraction Oasis MCX column.The separation of compounds was carried on an Eclipse Plus C18（RRHD 1.8 μm，2.1 mm×100 mm） by gradient elution using methanol-0.1% formic acid as mobile phase.The electrospray was operated in the positive mode and the samples were monitored under the multiple reaction monitoring（MRM） mode．The chromatographic retention time and mass fragment ion abundance ratio were taken for qualitative confirmation,and the internal standard method was employed for quantification analysis.The limits of detection（LOD） for both compounds were 0.05 μg/L,and the limits of quantitation（LOQ） were 0.2 μg/L in swine urine.The correlation coefficients of the swine urine were greater than 0.999（r2>0.999） within 0.2-20.0 μg/L linear ranges.Recoveries of amantadine and rimantadine at spiked levels of 0.5-20.0 μg/L were in the range of 89.7%-102.8% with intra-day relative standard deviation（RSDs） of 2.8%-4.2%. |
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