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Magnetic ionic liquids as versatile extraction phases for the rapid determination of estrogens in human urine by dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography-diode array detection

机译:磁离子液体作为多功能提取阶段,通过分散液 - 液微萃取与高性能液相色谱 - 二极管阵列检测的快速测定人尿中雌激素的快速测定

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摘要

In this study, a rapid and straightforward approach based on magnetic ionic liquids (MIL) as extraction phases and dispersive liquid-liquid microextraction (DLLME) was developed to analyze the hormones estriol, 17-beta-estradiol, 17-alpha-ethynylestradiol, and estrone in human urine samples. This is the first report of an application of manganese-based MILs compatible with HPLC to extract compounds of biological interest from urine samples. The hydrophobic MILs trihexyltetradecylphosphonium tetrachloromanganate (II) ([P-6,P-6,P-6,P-14 (+)](2)[MnCl4 (2-)]) and aliquat tetrachloromanganate (II) ([Aliquat(+)](2)[MnCl4 (2-)]) were employed and the optimized extraction conditions were comprised of 5 mg of MIL ([P-6,P-6,P-6,P-14 (+)](2)[MnCl4 (2-)]), 5 mu L of methanol (MeOH) as disperser solvent, and an extraction time of 90 s at sample pH 6. The analytical parameters of merit were determined under optimized conditions and very satisfactory results were achieved, with LODs of 2 ng mL(-1) for all analytes, determination coefficients (R (2)) ranging from 0.9949 for 17-beta-estradiol to 0.9998 for estrone. In addition, good results of method precision were achieved with the intraday (n = 3) varying from 4.7% for 17-beta-estradiol to 19.5% for estriol (both at 5 ng mL(-1)) and interday precision (evaluated at 100 ng mL(-1)) ranging from 11.4% for estrone to 17.7% for 17-alpha-ethynylestradiol and analyte relative recovery evaluated in three real samples ranged from 67.5 to 115.6%. The proposed DLLME/MIL-based approach allowed for a reliable, environmentally friendly and high-throughput methodology with no need for a centrifugation step.
机译:在该研究中,开发了基于磁离子液体(MIL)作为萃取阶段和分散液 - 液体微萃取(DLLME)的快速和直接的方法,以分析激素雌二醇,17-β-雌二醇,17-α-乙炔雌二醇和雌激素在人类尿液样本中。这是第一份与HPLC相容的锰的米尔应用,以提取来自尿液样品的生物学浓度化合物。疏水性密耳三氧基三乙二基鏻四氯壬酸盐(II)([P-6,P-6,P-6,P-14(+)](2))[MnCl4(2-)]和Aliquat Tothloromanganate(II)([Aliquat( +)](2)使用[MnCl 4(2-)]),优化的提取条件为5mg静电([P-6,P-6,P-6,P-14(+)]( 2)[MnCl4(2-)]),5μl甲醇(MeOH)作为分散剂溶剂,以及在样品pH6处的90s的提取时间。在优化条件下测定优异的分析参数,结果非常令人满意对于所有分析物,含有2ng ml(-1)的橡胶,测定系数(r(2))从0.9949到17-β-雌二醇为0.9998的雌激素。此外,通过对17-β-雌二醇的3.7%的盘子内(n = 3)实现了方法精度的良好结果,雌二醇的19.5%(均为5ng ml(-1))和中间的精度(评估100ng ml(-1))从雌激素的11.4%的范围为17.7%,在三个真实样品中评价的17-α-乙炔雌二醇和分析物相对恢复的范围为67.5至115.6%。所提出的DLLME / MIL的方法允许可靠,环保和高通量的方法,无需离心步骤。

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