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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >A novel headspace solid-phase microextraction method using in situ derivatization and a diethoxydiphenylsilane fibre for the gas chromatography-mass spectrometry determination of urinary hydroxy polycyclic aromatic hydrocarbons
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A novel headspace solid-phase microextraction method using in situ derivatization and a diethoxydiphenylsilane fibre for the gas chromatography-mass spectrometry determination of urinary hydroxy polycyclic aromatic hydrocarbons

机译:气相色谱-质谱法测定尿中羟基多环芳烃的顶空固相微萃取-原位衍生化和二乙氧基二苯基硅烷纤维

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摘要

An innovative and simple headspace solid-phase microextraction method using a novel diethoxy-diphenylsilane fibre based on in situ derivatization with acetic anhydride was optimized and validated for the gas chromatography-mass spectrometry determination of some monohydroxy metabolites of polycyclic aromatic hydrocarbons, namely 1 -hydroxynaphthalene, 2-hydroxynaphtalene, 9-hydroxyfluorene, 2-hydroxyfluorene and 1-hydroxypyrene at trace levels in human urine. Enzymatic hydrolysis was applied before derivatization, whereas extraction conditions, i.e. the effects of time and temperature of extraction and salt addition were investigated by experimental design. Regression models and desirability functions were applied to find the experimental conditions providing the highest global extraction response. These conditions were found in correspondence of an extraction temperature of 90 degrees C, an extraction time of 90 min and 25% NaCl added to urine samples. The capabilities of the developed method were proved obtaining limit of quantitations in the 0.1-2 mu g/l range, thus allowing the bio-monitoring of these compounds in human urine. A good precision was observed both in terms of intra-batch and inter-batch repeatability with RSD always lower than 14%. Recoveries ranging from 98(+/- 3) to 121(+/- 1)% and extraction yields higher than 72% were also obtained. Finally, the analysis of urine specimens of coke-oven workers revealed analytes' concentrations in the 2.2-164 mu g/l range, proving the exposure to PAHs of the involved workers.
机译:基于乙酸酐原位衍生化的新型二乙氧基-二苯基硅烷纤维的新颖,简单的顶空固相微萃取方法得到了优化,并通过气相色谱-质谱法测定了多环芳烃中的一些单羟基代谢物,即1-羟基萘。人尿中痕量的2-羟基萘,9-羟基芴,2-羟基芴和1-羟基py。衍生化之前先进行酶水解,然后通过实验设计研究提取条件,即提取时间和温度以及添加盐的影响。应用回归模型和合意函数来找到提供最高整体提取响应的实验条件。发现这些条件对应于提取温度为90摄氏度,提取时间为90分钟和添加到尿液样本中的25%氯化钠。事实证明,所开发方法的能力获得了0.1-2μg / l范围内的定量限,从而可以对人尿中的这些化合物进行生物监测。在批内和批间重复性方面均观察到良好的精度,RSD始终低于14%。回收率从98(+/- 3)%到121(+/- 1)%,提取率也高于72%。最后,对焦炉工人的尿液标本进行分析后发现,分析物的浓度在2.2-164微克/升的范围内,证明了相关工人暴露于多环芳烃中。

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