Nuñez Alberto, Lehotay Steven J, Geis-Asteggiante Lucía
US Department of Agriculture, Agricultural Research Service, Eastern Regional Research Center, 600 East Mermaid Lane, Wyndmoor, PA 19038, USA.
Cátedra de Farmacognosia y Productos Naturales, DQO, Facultad de Química, UdelaR, 2124 General Flores, Montevideo12800, Uruguay.
Rapid Commun Mass Spectrom. 2015 Apr 30;29(8):719-29. doi: 10.1002/rcm.7153.
Analysis for identification and quantification of regulated veterinary drug residues in foods is usually achieved by liquid chromatography coupled to tandem mass spectrometry (LC/MS/MS). The instrumental method requires the selection of characteristic ions, but structural elucidation is seldom performed to help ensure accuracy. This study is a continuation of previous work to characterize selected product ions in support of regulatory monitoring programs.
The tandem mass spectra of 28 veterinary drugs from a previously published LC/MS/MS method were acquired with a high-resolution quadrupole time-of-flight (Q-TOF) mass spectrometer using electrospray ionization (ESI) in positive mode. The TOF analyzer was calibrated to achieve a mass accuracy error <5 ppm for the MS and MS/MS modes, and samples were infused for data acquisition.
The high mass accuracy achieved in Q-TOF allowed elucidation of the formulae of the product ions previously selected for qualitative identification. Rational interpretation of results was made and compared with the published literature, and the structure for the MS/MS product ions of four classes of regulated drugs (mectins, benzimidazoles, nitroimidazoles, and phenothiazines), totaling 28 compounds, were examined leading to the report of new structures or confirmation of published structures using low-resolution MS.
Structural characterization of the product ions selected for identification and quantification of veterinary drug residues is important information for regulatory monitoring programs in defense of regulatory enforcement actions. This study has allowed structural elucidation of 84 MS/MS product ions previously selected for the LC/MS/MS analysis of 28 drug analytes.
食品中兽药残留的鉴定和定量分析通常采用液相色谱-串联质谱法(LC/MS/MS)。该仪器方法需要选择特征离子,但很少进行结构解析以确保准确性。本研究是先前工作的延续,旨在表征选定的产物离子,以支持监管监测计划。
使用高分辨率四极杆飞行时间(Q-TOF)质谱仪,在正模式下采用电喷雾电离(ESI),获取先前发表的LC/MS/MS方法中28种兽药的串联质谱图。对TOF分析仪进行校准,使MS和MS/MS模式下的质量准确度误差<5 ppm,并注入样品进行数据采集。
Q-TOF实现的高质量准确度允许阐明先前为定性鉴定而选择的产物离子的分子式。对结果进行了合理的解释,并与已发表的文献进行了比较,研究了四类受监管药物(莫昔克丁、苯并咪唑、硝基咪唑和吩噻嗪)共28种化合物的MS/MS产物离子结构,从而报告了新结构或使用低分辨率MS确认了已发表的结构。
为兽药残留的鉴定和定量选择的产物离子的结构表征是监管监测计划中支持监管执法行动的重要信息。本研究已对先前为28种药物分析物的LC/MS/MS分析选择的84个MS/MS产物离子进行了结构解析。