4.7 Article

Determination of steroid sex hormones in real matrices by bar adsorptive microextraction (BAμE)

期刊

TALANTA
卷 136, 期 -, 页码 145-154

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2014.11.013

关键词

Floating sampling technology; Sorbent phases; Steroid sex hormones; High performance liquid chromatography; Water matrices; Urine matrices

资金

  1. Fundacao para a Ciencia e a Tecnologia (Portugal) [PEst-OE/QUI/UI0612/2013]
  2. [SFRH/BD/69951/2010]
  3. Fundação para a Ciência e a Tecnologia [SFRH/BD/69951/2010] Funding Source: FCT

向作者/读者索取更多资源

In the present work, the development of a novel analytical approach which combines a miniaturized bar adsorptive microextraction device with a micro-liquid desorption in one single step, followed by high performance liquid chromatography with diode array detection (BA mu E-mu LD/HPLC-DAD), is proposed for the determination of trace levels of nine steroid hormones (estriol, 17 beta-estradiol, 17 alpha-estradiol, 19-northisterone, 17 alpha-ethynylestradiol, estrone, D-(-)-norgestrel, progesterone and mestranol) in environmental and biological matrices. From the comparison of ten different coating phases (five polymeric and five activated carbon sorbents), the modified pyrrolidone polymer (P2) showed the best compromise between selectivity and efficiency. Assays performed through BA mu E(P2, 1.3 mg)-mu LD(100 mu L)/HPLC-DAD on 25 mL of ultrapure water samples spiked at the 6.0 mu g/L level, yielded recoveries ranging from 93 +/- 9% to 101 +/- 8%, under optimized experimental conditions. The analytical performance showed convenient detection (50.0-100.0 ng/L) and quantification limits (165.0-330.0 ng/L), as well as good linear dynamic ranges (0.2-24.0 mu g/L) with remarkable determination coefficients (r(2) > 0.9968). Excellent repeatability were also achieved through intraday (RSD < 14%) and interday (RSD < 12%) experiments. The application of the proposed analytical approach on environmental water and urine samples, using the standard addition methodology (SAM), revealed good linearity and sensitivity at trace level, with the detection of some of the target compounds. In short, the miniaturization of the analytical device for microextraction combined with the minimization of the solvent volume for back-extraction in one single step demonstrated remarkable performance, increasing the enrichment factor, being simultaneously more easier to implement and environment friendly. (C) 2014 Elsevier B.V. All rights reserved.

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