Simultaneous Determination of 20 Illegally Added Drugs in Disinfection Products by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
Scientific Papers|更新时间:2025-12-03
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Simultaneous Determination of 20 Illegally Added Drugs in Disinfection Products by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
Journal of Instrumental AnalysisVol. 44, Issue 12, Pages: 2516-2525(2025)
ZHAO Zi-wei,ZHAN Zi-yue,DAI Yan-yu,XIE Ji-an,DING Gang,XU Qing-hua,LIU Bo-lin.Simultaneous Determination of 20 Illegally Added Drugs in Disinfection Products by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry[J].Journal of Instrumental Analysis,2025,44(12):2516-2525.
ZHAO Zi-wei,ZHAN Zi-yue,DAI Yan-yu,XIE Ji-an,DING Gang,XU Qing-hua,LIU Bo-lin.Simultaneous Determination of 20 Illegally Added Drugs in Disinfection Products by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry[J].Journal of Instrumental Analysis,2025,44(12):2516-2525. DOI: 10.12452/j.fxcsxb.250413288.
Simultaneous Determination of 20 Illegally Added Drugs in Disinfection Products by Modified QuEChERS/Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
An analytical method using ultra high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established for the simultaneous d
etermination of 20 illegally added drugs in disinfection products. Three dosage forms of samples were dispersed by water induction,extracted with acidified methanol,and purified with N-propyl ethylenediamine(PSA) adsorbent. The 20 target analytes were separated on a Waters Acquity
TM
UPLC BEH C
18
column(100 mm×2.1 mm,1.7 μm) with 0.05% formic acid water and 0.05% formic acid acetonitrile solution as mobile phase. The data were acquired using an electrospray ionization(ESI) source with positive/negative switching mode under multiple reaction monitoring(MRM),and quantified via the isotope internal standards. The 20 analytes exhibited good linearity in their respective mass concentration ranges,with correlation coefficients(
r
²) of 0.999 4-0.999 9. The method detection limits(LODs) ranged from 0.5 µg/kg to 10.0 µg/kg,and the method quantification limits(LOQs) were 1.25-25.0 µg/kg. The spiked recovery tests were conducted at low,medium and high levels,showing average recoveries of 84.5%-109% and relative standard deviations(RSDs,
n
=6) of 0.22%-8.4%. The established analytical method was applied to the determination of actual samples,and 8 samples were detected with illegal drugs. With simplified pretreatment,high purification efficiency,and short analytical runtime,the developed method achieves superior sensitivity and selectivity. It is capable of simultaneously meeting the requirements for both qualitative screening and quantitative analysis. It can be used for rapid analysis of various illegally added drugs in a large number of disinfection products.
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