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首页> 外文期刊>Journal of separation science. >Multiple monolithic fiber solid-phase microextraction based on a polymeric ionic liquid with high-performance liquid chromatography for the determination of steroid sex hormones in water and urine
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Multiple monolithic fiber solid-phase microextraction based on a polymeric ionic liquid with high-performance liquid chromatography for the determination of steroid sex hormones in water and urine

机译:基于聚合物离子液体和高效液相色谱的多重整体纤维固相微萃取法测定水和尿中的类固醇性激素

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摘要

The development of a simple and sensitive analytical approach that combines multiple monolithic fiber solid-phase microextraction with liquid desorption followed by high-performance liquid chromatography with diode array detection is proposed for the determination of trace levels of seven steroid sex hormones (estriol, 17 beta-estradiol, testosterone, ethinylestradiol, estrone, progesterone and mestranol) in water and urine matrices. To extract the target analytes effectively, multiple monolithic fiber solid-phase microextraction based on a polymeric ionic liquid was used to concentrate hormones. Several key extraction parameters including desorption solvent, extraction and desorption time, pH value and ionic strength in sample matrix were investigated in detail. Under the optimal experimental conditions, the limits of detection were found to be in the range of 0.027-0.12 mu g/L. The linear range was 0.10-200 mu g/L for 17 beta-estradiol, 0.25-200 mu g/L estriol, ethinylestradiol and estrone, and 0.50-200 mu g/L for the other hormones. Satisfactory linearities were achieved for analytes with the correlation coefficients above 0.99. Acceptable method reproducibility was achieved by evaluating the repeatability and intermediate precision with relative standard deviations of both less than 8%. The enrichment factors ranged from 54- to 74-fold. Finally, the proposed method was successfully applied to the analysis of steroid sex hormones in environmental water samples and human urines with spiking recoveries ranged from 75.6 to 116%.
机译:提出了一种简单而灵敏的分析方法的开发方法,该方法结合了多个整体纤维固相微萃取与液体脱附,然后结合高效液相色谱和二极管阵列检测技术,用于测定痕量的七种甾体性激素(雌三醇,17β -雌二醇,睾丸激素,炔雌醇,雌酮,孕酮和雌二醇)在水和尿液基质中的含量。为了有效地提取目标分析物,使用了基于聚合物离子液体的多次整体纤维固相微萃取来浓缩激素。详细研究了几个关键的萃取参数,包括脱附溶剂,萃取和脱附时间,pH值和样品基质中的离子强度。在最佳实验条件下,检测限为0.027-0.12μg / L。 17种β-雌二醇的线性范围为0.10-200μg / L,雌三醇,乙炔基雌二醇和雌酮的线性范围为0.25-200μg/ L,其他激素的线性范围为0.50-200μg/ L。对于相关系数高于0.99的分析物,获得了令人满意的线性。通过评估相对标准偏差均小于8%的可重复性和中间精度,可以实现可接受的方法重现性。富集因子范围为54到74倍。最终,该方法成功用于环境水样和人尿中类固醇性激素的分析,加标回收率在75.6%至116%之间。

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