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摘要
A new method was developed for the rapid screening and confirmation analysis of barbital, amobarbital and phenobarbital residues in pork by gas chromatography-tandem mass spectrometry (GC/MS/MS) with ion trap MSD. The residual barbiturates in pork were extracted by ultrasonic extraction, cleaned up on a multiwalled carbon nanotubes (MWCNTs) packed solid phase extraction (SPE) cartridge and applied acetone-ethyl acetate (3:7, v/v) mixture as eluting solvent and derivatized With CH3I under microwave irradiation. The methylated barbiturates were separated on a TR-5MS capillary column and detected with an ion trap mass detector. Electron impact ion source (El) operating MS/MS mode was adopted for identification and external standard method was employed for quantification. One precursor ion m/z. 169 was selected for analysis of barbital and amobarbital and m/z 232 was selected for phenobarbital. The product ions were obtained under 1.0 V excitation voltage. Good linearities (linear coefficient R > 0.99) were obtained at the range of 0.5-50 mu g kg(-1). Limit of detection (LOD) of barbital was 0.2 mu g kg(-1) and that of amobarbital and phenobarbital were both 0.1 mu gkg(-1) (S/N >= 3). Limit of qualification (LOQ) was 0.5 mu g kg(-1) for three barbiturates (S/N >= 10). Satisfying recoveries ranging from 75% to 96% of the three barbiturates spiked in pork were obtained, with relative standard deviations (R.S.D.) in the range of 2.1-7.8%.
- 出版日期2007-3-14
- 单位中国农业大学; 中国检验检疫科学研究院; 河北北方学院
