Saleh Abolfazl, Yamini Yadollah, Faraji Mohammad, Shariati Shahab, Rezaee Mohammad
Department of Chemistry, Tarbiat Modares University, Tehran, Iran.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Jun 15;877(18-19):1758-64. doi: 10.1016/j.jchromb.2009.04.039. Epub 2009 May 3.
In the present work, a simple and high sensitive method based on hollow fiber liquid phase microextraction (HF-LPME) was developed followed by high performance liquid chromatography (HPLC) for determination of ultra-trace amounts of Se(IV) after derivatization in biological and natural water samples. Se(IV) was complexed with o-phenylenediamine to form piazselenol. The formed piazselenol was extracted into 20 microL of 1-octanol located in the lumen of a hollow fiber and the solution was injected into HPLC-UV for analysis. Using the Taguchi method, an orthogonal array design (OAD), OA(16) (4(5)) was employed to optimize the HF-LPME of piazselenol. The effect of five experimental factors (each factor at four levels) including the volume of the organic phase, extraction time, pH of the solution, stirring rate and ionic strength on the extraction efficiency of piazselenol was studied and optimized. The maximum extraction efficiency of piazselenol was obtained at 20 microL of 1-octanol as the extracting solvent, 30 min extraction time, pH 2, stirring rate of 500 rpm and 30% (w/v) NaCl. Under the optimum conditions, preconcentration factors up to 130 were achieved and the relative standard deviation (%RSD) of the method was <3.7% for different concentrations of Se(IV). The calibration curves were obtained in the ranges of 0.2-100 and 0.05-10 microgL(-1) for the 11 and 50 mL of the sample volumes with reasonable linearity, respectively (r(2)> 0.995). The limits of detection (LOD) were 0.1 and 0.02 microgL(-1) for the 11 and 50 mL sample volumes, respectively (S/N - 3). Finally, the applicability of the proposed method was evaluated by the extraction and determination of Se(IV) in the plasma, urine and water samples.
在本研究中,开发了一种基于中空纤维液相微萃取(HF-LPME)的简单且高灵敏度的方法,随后结合高效液相色谱(HPLC)用于测定生物和天然水样中痕量硒(IV)经衍生化后的含量。硒(IV)与邻苯二胺络合形成硒吩。形成的硒吩被萃取到位于中空纤维内腔的20 μL 1-辛醇中,然后将溶液注入HPLC-UV进行分析。采用田口方法,使用正交阵列设计(OAD),即OA(16) (4(5))来优化硒吩的HF-LPME。研究并优化了五个实验因素(每个因素有四个水平),包括有机相体积、萃取时间、溶液pH值、搅拌速率和离子强度对硒吩萃取效率的影响。以20 μL 1-辛醇作为萃取溶剂、萃取时间30分钟、pH值为2、搅拌速率500 rpm和30%(w/v)NaCl时,硒吩的萃取效率最高。在最佳条件下,富集因子高达130,该方法对不同浓度硒(IV)的相对标准偏差(%RSD)<3.7%。对于11 mL和50 mL的样品体积,校准曲线分别在0.2 - 100和0.05 - 10 μg L⁻¹范围内获得,具有合理的线性关系(r²>0.995)。对于11 mL和50 mL的样品体积,检测限(LOD)分别为0.1和0.02 μg L⁻¹(S/N = 3)。最后,通过对血浆、尿液和水样中硒(IV)的萃取和测定,评估了该方法的适用性。