Almeida C, Nogueira J M F
University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department and Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.
University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department and Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.
Talanta. 2015 May;136:145-54. doi: 10.1016/j.talanta.2014.11.013. Epub 2014 Nov 15.
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 (BAµE-µLD/HPLC-DAD), is proposed for the determination of trace levels of nine steroid hormones (estriol, 17ß-estradiol, 17α-estradiol, 19-northisterone, 17α-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 BAµE(P2, 1.3mg)-µLD(100µL)/HPLC-DAD on 25mL of ultrapure water samples spiked at the 6.0μg/L level, yielded recoveries ranging from 93±9% to 101±8%, under optimized experimental conditions. The analytical performance showed convenient detection (50.0-100.0ng/L) and quantification limits (165.0-330.0ng/L), as well as good linear dynamic ranges (0.2-24.0µg/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.
在本研究中,提出了一种新型分析方法,该方法将微型棒吸附微萃取装置与微液解吸在一步中结合,随后进行带二极管阵列检测的高效液相色谱法(BAµE-µLD/HPLC-DAD),用于测定环境和生物基质中痕量水平的九种甾体激素(雌三醇、17β-雌二醇、17α-雌二醇、19-去甲睾酮、17α-乙炔雌二醇、雌酮、D-(-)-炔诺孕酮、孕酮和炔雌醇甲醚)。通过比较十种不同的涂层相(五种聚合物和五种活性炭吸附剂),改性吡咯烷酮聚合物(P2)在选择性和效率之间表现出最佳的平衡。在优化的实验条件下,对25mL加标浓度为6.0μg/L的超纯水样品进行BAµE(P2, 1.3mg)-µLD(100µL)/HPLC-DAD分析,回收率在93±9%至101±8%之间。分析性能显示出方便的检测限(50.0 - 100.0ng/L)和定量限(165.0 - 330.0ng/L),以及良好的线性动态范围(0.2 - 24.0µg/L),测定系数显著(r(2)>0.9968)。通过日内(RSD<14%)和日间(RSD<12%)实验也实现了出色的重复性。使用标准加入法(SAM)将所提出的分析方法应用于环境水和尿液样品,在痕量水平下显示出良好的线性和灵敏度,并检测到了一些目标化合物。简而言之,用于微萃取的分析装置的小型化与一步反萃取溶剂体积的最小化相结合,表现出卓越的性能,提高了富集因子,同时更易于实施且环境友好。