Gao Fudie, Zhao Yan, Shao Bing, Zhang Jing
School of Public Health and Family Medicine, Capital Medical University, Beijing 100069, China.
Se Pu. 2012 Jun;30(6):560-7. doi: 10.3724/sp.j.1123.2012.02021.
An analytical method was established for the simultaneous determination of 42 pesticides and veterinary drugs in milk by ultra performance liquid chromatography coupled with quadrupole-time of flight mass spectrometry (UPLC-Q-TOF-MS). The target compounds are the commonly used drugs including 13 pesticides and 29 veterinary drugs. The QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) method was used for sample preparation. The analytes in milk samples were extracted with acetonitrile containing 1.0% (v/v) formic acid, and were salted out by adding anhydrous sodium sulfate and potassium chloride. After that, the extract solution was purified by dispersive solid phase extraction with C18 sorbent. In the chromatographic analysis of 42 target compounds were separated on an ACQUITY UPLC BEH C18 column with the gradient elution using the mobile phases of acetonitrile and water containing 0.1% formic acid. MS(E) (where E represents collision energy) acquisition under positive ion mode was performed to obtain accurate relative molecular masses and fragment ions. As a result, the limits of quantification (LOQ, S/N = 10) of the target compounds were from 1 microg/kg to 100 microg/kg in milk. The average recoveries of the 42 analytes spiked at three concentration levels were ranged from 68.2% to 129.1% with the relative standard deviations of 2.8% - 30.8%. This method can be applied to the analysis of the 42 pesticides and veterinary drugs in milk due to its fastness, simplicity and relatively high sensitivity.
建立了一种超高效液相色谱-四极杆飞行时间质谱联用(UPLC-Q-TOF-MS)同时测定牛奶中42种农药和兽药的分析方法。目标化合物为常用药物,包括13种农药和29种兽药。采用QuEChERS(快速、简便、廉价、有效、耐用、安全)方法进行样品制备。牛奶样品中的分析物用含1.0%(v/v)甲酸的乙腈提取,加入无水硫酸钠和氯化钾进行盐析。之后,提取液用C18吸附剂通过分散固相萃取进行净化。在色谱分析中,42种目标化合物在ACQUITY UPLC BEH C18柱上分离,采用乙腈和含0.1%甲酸的水作为流动相进行梯度洗脱。在正离子模式下进行MS(E)(其中E代表碰撞能量)采集,以获得准确的相对分子质量和碎片离子。结果表明,目标化合物在牛奶中的定量限(LOQ,S/N = 10)为1 μg/kg至100 μg/kg。42种分析物在三个浓度水平加标的平均回收率为68.2%至129.1%,相对标准偏差为2.8% - 30.8%。该方法快速、简便且灵敏度较高,可以应用于牛奶中42种农药和兽药的分析。