AI Article Synopsis
- The study developed a method for detecting six benzodiazepine sedatives in aquatic products using high-performance liquid chromatography and mass spectrometry.
- Samples were extracted with acetonitrile, purified, and analyzed, showing a strong linear correlation for the sedatives across a specific concentration range.
- The method proved to be effective and reliable, with recoveries between 74.2% to 108.0% and low detection limits, making it suitable for monitoring these sedatives in food products.
Article Abstract
Objective: To establish a method for the simultaneous determination of 6 benzodiazepine sedatives residue in aquatic products by high performance liquid chromatography-triple quadrupole mass spectrometry.
Methods: The samples were extracted with acetonitrile and purified by C_(18 )solid phase extraction column. The sample solution was separated by Waters ACQUITY UPLC BEH C_(18 )column(2.1 mm×50 mm, 1.7 μm) using 0.1% formic acid and methanol as mobile phase for gradient elution, determined in multiple reaction monitoring mode and quantified by internal standard method.
Results: Six benzodiazepine sedatives had a good linear relationship in the range of 1.0-50.0 μg/L with r>0.9990, the limits of detection and limits of quantification were 0.3 and 1.0 μg/kg. Average recoveries for the analytes at 3 spiked levels ranged from 74.2%-108.0% with relative standard deviations of 1.1%-6.7%(n=6).
Conclusion: The method is simple, rapid, sensitive and accurate, which is suitable for simultaneous determination of 6 benzodiazepine sedatives residue in aquatic products.
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| http://dx.doi.org/10.19813/j.cnki.weishengyanjiu.2024.02.017 | DOI Listing |
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