Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Química, Universidad de La Laguna (ULL), Avenida Astrofísico Francisco Sánchez, s/n° 38206 La Laguna, Tenerife, Spain.
J Chromatogr A. 2013 Oct 25;1313:166-74. doi: 10.1016/j.chroma.2013.05.081. Epub 2013 Jun 10.
A new method based on hollow-fiber liquid-phase microextraction (HF-LPME) has been developed for the determination of a group of organophosphorus pesticides, including some of their metabolites, in two commercial cereal-based baby foods and one wheat flour prior to gas chromatography-nitrogen phosphorus detection. Samples were first extracted by ultrasound-assisted extraction with acetonitrile (ACN) containing 1.25% (v/v) of formic acid. After evaporation and reconstitution in Milli-Q water, the HF-LPME procedure, using 1-octanol as extraction solvent, was applied followed by a desorption step in ACN, which clearly improved the performance of the technique. The effects of sample pH, ionic strength, stirring rate, extraction temperature and time as well as the desorption procedure were investigated. Under the optimum conditions that involved the extraction of the analytes from 10 mL of the water reconstituted extract at pH 7.0 containing 5% (w/v) of NaCl for 45 min at 960 rpm, the method was validated in terms of linearity, precision and accuracy. The limits of detection (LODs) were between 0.29 and 3.20 μg/kg. The extraction of Milli-Q water, as an example of the applicability of the procedure to aqueous samples, allowed achieving LODs in the range 0.01-0.04 μg/L. Such values, together with the ones achieved for the rest of the samples, are below or equal to the maximum residue limits specified by the European Union.
一种新的基于中空纤维液相微萃取(HF-LPME)的方法已经被开发出来,用于在气相色谱-氮磷检测前,从两种商业谷物婴儿食品和一种小麦面粉中测定一组有机磷农药,包括它们的一些代谢物。样品首先用含有 1.25%(v/v)甲酸的乙腈(ACN)通过超声辅助提取进行提取。在蒸发并在 Milli-Q 水中重新配制后,应用 HF-LPME 程序,使用 1-辛醇作为萃取溶剂,然后在 ACN 中进行解吸步骤,这明显改善了技术性能。考察了样品 pH 值、离子强度、搅拌速度、萃取温度和时间以及解吸程序的影响。在最佳条件下,从 pH 值为 7.0、含 5%(w/v)NaCl 的 10 mL 水重提液中,在 960 rpm 下萃取 45 min,对该方法进行了线性、精密度和准确度验证。检测限(LOD)在 0.29 至 3.20 μg/kg 之间。作为该程序适用于水样的适用性实例,对 Milli-Q 水的萃取可以达到 0.01-0.04 μg/L 的检测限。这些值,以及其余样品的检测限,均低于或等于欧盟规定的最大残留限量。