Shamsipur Mojtaba, Yazdanfar Najmeh, Ghambarian Mahnaz
Department Chemistry, Razi University, Kermanshah, Iran.
Department Chemistry, Razi University, Kermanshah, Iran; Iranian Research and Development Center for Chemical Industries, ACECR, Tehran, Iran.
Food Chem. 2016 Aug 1;204:289-297. doi: 10.1016/j.foodchem.2016.02.090. Epub 2016 Feb 15.
In this work, an effective preconcentration method for the extraction and determination of traces of multi-residue pesticides was developed using solid-phase extraction (SPE) coupled with dispersive liquid-liquid microextraction and gas chromatography-mass spectrometry (GC-MS). Variables affecting the performance of both extraction steps such as type and volume of elution and extraction solvents, breakthrough volume, salt addition, extraction time were thoroughly investigated. The proposed method resulted in good linearities (R(2)>0.9915) over the ranges of 1-10,000ngkg(-1), limits of detection (LODs) in the range of 0.5-1.0ngkg(-1) at S/N=3, and precision of RSD% of ⩽11.8. Under optimal conditions, the preconcentration factors were obtained in the range of 2362-10,593 for 100mL sample solutions. Comparison of the proposed method with other ones demonstrated that SPE-DLLME method provides higher extraction efficiency and larger preconcentration factor for determination of pesticides residues. Further, it is simple, inexpensive, highly sensitive, and can be successfully applied to separation, preconcentration and determination of the pesticides (and other noxious materials) in different real food samples.
在本研究中,开发了一种有效的预浓缩方法,用于提取和测定痕量多残留农药,该方法采用固相萃取(SPE)结合分散液液微萃取和气相色谱-质谱联用(GC-MS)。对影响两个萃取步骤性能的变量,如洗脱溶剂和萃取溶剂的类型及体积、穿透体积、加盐量、萃取时间等进行了全面研究。所提出的方法在1-10,000 ng kg(-1)范围内具有良好的线性(R(2)>0.9915),在S/N = 3时检测限(LOD)在0.5-1.0 ng kg(-1)范围内,相对标准偏差(RSD%)精度≤11.8。在最佳条件下,对于100 mL样品溶液,预浓缩因子在2362-10,593范围内。将所提出的方法与其他方法进行比较表明,SPE-DLLME方法在测定农药残留方面具有更高的萃取效率和更大的预浓缩因子。此外,该方法简单、廉价、高度灵敏,可成功应用于不同实际食品样品中农药(及其他有害物质)的分离、预浓缩和测定。