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首页> 外文期刊>Archives of Toxicology >Selective determination of mandelic acid in urine using molecularly imprinted polymer in microextraction by packed sorbent
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Selective determination of mandelic acid in urine using molecularly imprinted polymer in microextraction by packed sorbent

机译:用填充吸附剂在微萃取中使用分子印迹聚合物的尿液中尿酸的选择性测定

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摘要

Mandelic acid (MA) is a major metabolite of ethylbenzene and styrene. For the first time, a selective, fast, and easy-to-use procedure was developed for the determination of MA in urine samples. The new procedure is based on MIMEPS, the combination of a molecularly imprinted polymer (MIP) and microextraction by packed sorbent (MEPS). High-performance liquid chromatography with ultraviolet detection (HPLC-UV) was used for the separation and determination of MA. The bulk polymerization method was used to synthesize the MIP, and the MIP and non-imprinted polymer (NIP) were characterized by Fourier transform infrared spectroscopy. The selectivity of the MIP was investigated in the presence of interferents. In addition, we investigated the various parameters that affect the performance of the MEPS, including the pH of the sample, the number of extraction cycles, sample volume, and the types and volumes of the washing and elution solvents. A six-point calibration curve was obtained in the range of 0.2-20 mu g/mL (R-2 = 0.9994). The extraction recovery was more than 88.8%. The limit of detection and the limit of quantitation were 0.06 and 0.2 mu g/mL, respectively. The intra- and inter-day precisions were in the range of 3.6-4.7% and 3.8-5.1%, respectively. The accuracy was -8.4 to -11.1%. The optimized procedure was selective, sensitive, and rapid, and it was both user friendly and environmentally friendly. The sample preparation process took only about 5 min, so the MIMEPS-HPLC-UV procedure is recommended as an alternative for the biomonitoring of workers exposed to ethylbenzene and/or styrene.
机译:少甲酸(ma)是乙苯和苯乙烯的主要代谢物。首次开发了一种选择性,快速,易于使用的程序,用于测定尿液样本中的MA。新程序基于MIMEPs,通过包装的吸附剂(MEP)的分子印迹聚合物(MIP)和微萃取的组合。具有紫外检测(HPLC-UV)的高效液相色谱法用于分离和测定MA。本体聚合方法用于合成MIP,通过傅里叶变换红外光谱表征MIP和非印记聚合物(NIP)。在干扰的存在下研究了MIP的选择性。此外,我们研究了影响MEPs性能的各种参数,包括样品的pH,提取循环,样品体积的数量和洗涤和洗脱溶剂的类型和体积。获得六点校准曲线在0.2-20μmg/ ml(R-2 = 0.9994)的范围内。提取回收率超过88.8%。检测极限和定量限分别为0.06和0.2μg/ ml。日内和日内的诊断分别为3.6-4.7%和3.8-5.1%。准确性为-8.4至-11.1%。优化的程序是选择性的,敏感的,快速,并且它既是用户友好和环保的。样品制备方法仅服用约5分钟,因此建议使用MIMEPS-HPLC-UV程序作为暴露于乙苯和/或苯乙烯的工人的生物监唱的替代方案。

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