Bo Haibo
Hebei Entry-Exit Inspection and Quarantine Bureau, Shijiazhuang 050051, China.
Se Pu. 2011 Feb;29(2):180-3. doi: 10.3724/sp.j.1123.2011.00180.
A sensitive and selective method is presented for the determination of paraquat residue in fruits, vegetables, beans and grain by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Paraquat in samples was extracted with water and cleaned-up with a weak cation exchange (WCX) column to obtain an extract suitable for analysis using HPLC-MS/MS. The paraquat was separated by a CAPCELL PAK ST column (150 mm x 2.0 mm) and with acetonitrile-10 mmol/L ammonium acetate solution (adjusted to pH 4.0 by formic acid) as the mobile phase, and multiple reaction monitoring (MRM) was used with electrospray ionization in the positive ion mode. The calibration curve was linear between the peak area and the mass concentration of paraquat from 0.01 to 0.1 mg/L with the correlation coefficient of 0.993. Recoveries of paraquat spiked in samples at three levels ranged from 84.0% to 106.0% with the relative standard deviations of 7.8% - 18.8%. The limits of detection (LODs) of paraquat were 0.01 mg/kg in fruits and vegetables and 0.05 mg/kg in beans and grain. The LODs can meet the requirements of international maximum residue limit.
建立了一种灵敏且具有选择性的方法,用于通过高效液相色谱-串联质谱法(HPLC-MS/MS)测定水果、蔬菜、豆类和谷物中的百草枯残留。样品中的百草枯用水萃取,并用弱阳离子交换(WCX)柱净化,以获得适合用HPLC-MS/MS分析的提取物。百草枯通过CAPCELL PAK ST柱(150 mm×2.0 mm)分离,以乙腈-10 mmol/L醋酸铵溶液(用甲酸调节至pH 4.0)为流动相,采用多反应监测(MRM),在正离子模式下进行电喷雾电离。百草枯的峰面积与质量浓度在0.01至0.1 mg/L之间呈线性关系,相关系数为0.993。样品中添加三个水平的百草枯的回收率在84.0%至106.0%之间,相对标准偏差为7.8% - 18.8%。水果和蔬菜中百草枯的检测限(LOD)为0.01 mg/kg,豆类和谷物中为0.05 mg/kg。这些检测限能够满足国际最大残留限量的要求。