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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Development of a method to profile 2-to 4-ring polycyclic aromatic hydrocarbons in saliva samples from smokers and non-smokers by headspace-solid-phase microextraction-gas chromatography-triple quadrupole tandem mass spectrometry
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Development of a method to profile 2-to 4-ring polycyclic aromatic hydrocarbons in saliva samples from smokers and non-smokers by headspace-solid-phase microextraction-gas chromatography-triple quadrupole tandem mass spectrometry

机译:通过顶空 - 固相微萃取 - 气相色谱 - 三重四极杆串联质谱法从吸烟者和非吸烟者划分唾液和非吸烟者样品中唾液样品中的方法2至4环多环芳烃烃的方法

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摘要

This study reports the development of a method based on headspace (HS)-solid-phase microextraction (SPME)gas chromatography (GC)-triple quadrupole tandem mass spectrometry (MS/MS) for the quantification of 2to 4-ring polycyclic aromatic hydrocarbons (PAHs) in saliva samples. Eight unmetabolized compounds (naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene and pyrene) were quantified using six deuterated PAHs as surrogate internal standards. The absence of matrix effect allowed saliva samples to be quantified by external calibration method. The optimized method resulted easy, with minimal sample pre-treatment (homogenization of the sample), and it achieved the highest sensitivity up to date: limits of quantification (LOQ) were in the 0.8-26.4 ng L-1 range, with a significant improvement in comparison with the few existing methods. Intraand inter-run precisions provided CV values < 18.1%, and accuracies within 20% of the spiked concentration. The application of the method to the analysis of fresh saliva samples collected by spitting from smokers (n = 10) and non-smokers (n = 10) showed that PAHs were quantifiable in all samples and that smokers had higher levels of all compounds than non-smokers. These results show that the method is suitable for quantifying low-boiling PAHs in saliva samples from individuals exposed at different PAH levels.
机译:本研究报告了一种基于顶空(HS)-固相微萃取(SPME)-气相色谱(GC)-三重四极杆串联质谱(MS/MS)的方法,用于唾液样品中2至4环多环芳烃(PAHs)的定量。使用六种氘化多环芳烃作为替代内标物,对八种未降解化合物(萘、苊、苊、芴、菲、蒽、荧蒽和芘)进行定量。由于没有基质效应,可以通过外部校准方法对唾液样本进行量化。优化后的方法简便易行,样品预处理(样品均匀化)最少,并达到了迄今为止最高的灵敏度:定量限(LOQ)在0.8-26.4 ng L-1范围内,与现有的几种方法相比有显著改进。批内和批间精密度提供的CV值小于18.1%,准确度在加标浓度的20%以内。将该方法应用于吸烟者(n=10)和非吸烟者(n=10)通过吐痰采集的新鲜唾液样本的分析表明,所有样本中的多环芳烃都是可量化的,吸烟者的所有化合物水平都高于非吸烟者。这些结果表明,该方法适用于定量不同PAH水平暴露个体唾液样品中的低沸点PAH。

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