A new dispersive liquid-liquid microextraction using ionic liquid based microemulsion coupled with cloud point extraction for determination of copper in serum and water samples

被引:49
作者
Arain, Salma Aslam [1 ]
Kazi, Tasneem Gul [1 ]
Afridi, Hassan Lmran [1 ]
Arain, Mariam Shahzadi [1 ]
Panhwar, Abdul Haleem [1 ]
Khan, Naeemullah [1 ]
Baig, Jameel Ahmed [1 ]
Shah, Faheem [2 ]
机构
[1] Univ Sindh, Natl Ctr Excellence Analyt Chem, Jamshoro 76080, Pakistan
[2] COMSATS Inst Informat Technol, Dept Chem, Abbottabad 22060, Pakistan
关键词
Copper; Ionic liquid; Dispersive liquid-liquid microextraction; Phase inversion method; Cloud point extraction; Flame atomic absorption spectrometry; ATOMIC-ABSORPTION-SPECTROMETRY; SOLID-PHASE EXTRACTION; ENVIRONMENTAL-SAMPLES; BIOLOGICAL SAMPLES; VIRAL-HEPATITIS; PRECONCENTRATION; COPRECIPITATION; OPTIMIZATION; MULTIVARIATE; MICELLES;
D O I
10.1016/j.ecoenv.2015.12.035
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A simple and rapid dispersive liquid-liquid microextraction procedure based on ionic liquid assisted microemulsion (IL-E-DLLME) combined with cloud point extraction has been developed for pre-concentration copper (Cu2+) in drinking water and serum samples of adolescent female hepatitits C (HCV) patients. In this method a ternary system was developed to form microemulsion ( mu E) by phase inversion method (PIM), using ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([C(4)mim][PF6]) and nonionic surfactant, TX-100 (as a stabilizer in aqueous media). The Ionic liquid microemulsion (IL-mu E) was evaluated through visual assessment, optical light microscope and spectrophotometrically. The Cu2+ in real water and aqueous acid digested serum samples were complexed with 8-hydroxyquinoline (oxine) and extracted into IL-mu E medium. The phase separation of stable IL - E was carried out by the micellar cloud point extraction approach. The influence of of different parameters such as pH, oxine concentration, centrifugation time and rate were investigated. At optimized experimental conditions, the limit of detection and enhancement factor were found to be 0.132 and 70 respectively, with relative standard deviation <5%. In order to validate the developed method, certified reference materials (SLRS-4 Riverine water) and human serum (Sero-M10181) were analyzed. The resulting data indicated a non -significant difference in obtained and certified values of Cu2+. The developed procedure was successfully applied for the preconcentration and determination of trace levels of Cu2+ in environmental and biological samples. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:186 / 192
页数:7
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