Rapid Screening Method for Detecting Ethinyl Estradiol in Natural Water Employing Voltammetry

被引:17
|
作者
Nunes, Chalder Nogueira [1 ]
Pauluk, Lucas Ely [1 ]
Felsner, Maria Lurdes [1 ]
dos Anjos, Vanessa Egea [2 ]
Quinaia, Sueli Percio [1 ]
机构
[1] Univ Estadual Centro Oeste, Dept Quim, BR-85040080 Guarapuava, PR, Brazil
[2] Univ Estadual Ponta Grossa, Dept Quim, BR-84030900 Ponta Grossa, PR, Brazil
关键词
ETHINYLESTRADIOL; EXPOSURE; 17-ALPHA-ETHYNYLESTRADIOL; 17-BETA-ESTRADIOL; ELECTRODE; SAMPLES;
D O I
10.1155/2016/3217080
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
17 alpha-Ethinyl estradiol (EE2), which is used worldwide in the treatment of some cancers and as a contraceptive, is often found in aquatic systems and is considered a pharmaceutically active compound (PhACs) in the environment. Current methods for the determination of this compound, such as chromatography, are expensive and lengthy and require large amounts of toxic organic solvents. In this work, a voltammetric procedure is developed and validated as a screening tool for detecting EE2 in water samples without prior extraction, clean-up, or derivatization steps. Application of the method we elaborate here to EE2 analysis is unprecedented. EE2 detection was carried out using differential pulse adsorptive cathodic stripping voltammetry (DP AdCSV) with a hanging mercury drop electrode (HMDE) in pH 7.0 Britton-Robinson buffer. The electrochemical process of EE2 reduction was investigated by cyclic voltammetry at different scan rates. Electroreduction of the hormone on a mercury electrode exhibited a peak at -1.16 +/- 0.02V versus Ag/AgCl. The experimental parameters were as follows: -0.7V accumulation potential, 150 s accumulation time, and 60mVs(-1) scanrate. The limit of detection was 0.49 mu gL(-1) for a preconcentration time of 150 s. Relative standard deviations were less than 13%. The method was applied to the detection of EE2 in water samples with recoveries ranging from 93.7 to 102.5%.
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页数:7
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