Diuzheva Alina, Balogh József, Jekő József, Cziáky Zoltán
Department of Analytical Chemistry, Faculty of Science, Pavol Jozef Šafárik University in Košice, Košice, Slovakia.
Department of Chemistry, University of Nyíregyháza, Nyíregyháza, Hungary.
J Sep Sci. 2018 Jul;41(14):2870-2877. doi: 10.1002/jssc.201800309. Epub 2018 Jun 10.
A dispersive liquid-liquid microextraction method for the simultaneous determination of 11 pharmaceuticals has been developed. The method is based on a microextraction procedure applied to wastewater samples from different regions of Hungary followed by high-performance liquid chromatography with mass spectrometry. The effect of the nature of the extractant, dispersive solvent, different additives, and extraction time were examined on the extraction efficiently of the dispersive liquid-liquid microextraction method. Under optimal conditions, the linearity for determining the pharmaceuticals was in the range of 1-500 ng/mL, with the correlation coefficients ranging from 0.9922 to 0.9995. The limits of detection and limits of quantification were in the range of 0.31-6.65 and 0.93-22.18 ng/mL, respectively.
已开发出一种用于同时测定11种药物的分散液液微萃取方法。该方法基于对匈牙利不同地区废水样品进行微萃取,随后采用高效液相色谱-质谱联用。考察了萃取剂性质、分散溶剂、不同添加剂和萃取时间对分散液液微萃取方法萃取效率的影响。在最佳条件下,测定药物的线性范围为1-500 ng/mL,相关系数在0.9922至0.9995之间。检测限和定量限分别在0.31-6.65和0.93-22.18 ng/mL范围内。