Facultad de Química, Departamento de Química Analítica, Universidad Nacional Autónoma de México, México, DF, 04510, México.
J Chromatogr A. 2011 Sep 28;1218(39):6869-77. doi: 10.1016/j.chroma.2011.08.011. Epub 2011 Aug 12.
A miniaturized method based on matrix solid-phase dispersion coupled to solid phase extraction and high performance liquid chromatography with diode array detection (MSPD-SPE-HPLC/DAD) was developed for the trace simultaneous determination of the following organophosphorus pesticides (OPPs) in bovine tissue: parathion-methyl, fenitrothion, parathion, chlorfenvinphos, diazinon, ethion, fenchlorphos, chlorpyrifos and carbophenothion. To perform the coupling between MSPD and SPE, 0.05 g of sample was dispersed with 0.2 g of C(18) silica sorbent and packed into a stainless steel cartridge containing 0.05 g of silica gel in the bottom. After a clean-up of high and medium polarity interferences with water and an acetonitrile:water mixture, the OPPs were desorbed from the MSPD cartridge with pure acetonitrile and directly transferred to a dynamic mixing chamber for dilution with water and preconcentration into an SPE 20 mm × 2.0 mm I.D. C(18) silica column. Subsequently, the OPPs were eluted on-line with the chromatographic mobile phase to the analytical column and the diode array detector for their separation and detection, respectively. The method was validated and yielded recovery values between 91% and 101% and precision values, expressed as relative standard deviations (RSD), which were less than or equal to 12%. Linearity was good and ranged from 0.5 to 10 μg g(-1), and the limits of detection of the OPPs were in the range of 0.04-0.25 μg g(-1). The method was satisfactorily applied to the analysis of real samples and is recommended for food control, research efforts when sample amounts are limited, and laboratories that have ordinary chromatographic instrumentation.
建立了一种基于基质固相分散(MSPD)与固相萃取(SPE)相结合并结合高效液相色谱-二极管阵列检测(HPLC/DAD)的微型化方法,用于痕量同时测定牛组织中的下列有机磷农药(OPPs):甲基对硫磷、杀螟硫磷、对硫磷、氯芬磷、二嗪磷、乙硫磷、苯氯磷、毒死蜱和苯硫磷。为了实现 MSPD 和 SPE 的偶联,将 0.05 g 样品与 0.2 g C(18)硅胶吸附剂分散,装入不锈钢管中,底部装有 0.05 g 硅胶。用高极性和中等极性的水和乙腈:水混合物对高和中等极性干扰物进行清洗后,用纯乙腈从 MSPD 管中洗脱 OPPs,并用纯乙腈直接转移到动态混合室中,用纯水稀释并在 SPE 20mm×2.0mmID C(18)硅胶柱中预浓缩。随后,用色谱流动相在线将 OPPs 洗脱到分析柱和二极管阵列检测器中,分别进行分离和检测。该方法经过验证,回收率在 91%至 101%之间,精密度以相对标准偏差(RSD)表示,小于或等于 12%。线性良好,范围为 0.5 至 10μg g(-1),OPPs 的检测限在 0.04 至 0.25μg g(-1)范围内。该方法可满意地应用于实际样品的分析,适用于食品安全控制、当样品量有限时的研究工作以及具有普通色谱仪器的实验室。