Analysis of aromatic amines in human urine using comprehensive multi-dimensional gas chromatography-mass spectrometry (GCxGC-MS)

IF 4.5 2区 医学 Q1 INFECTIOUS DISEASES International journal of hygiene and environmental health Pub Date : 2024-02-28 DOI:10.1016/j.ijheh.2024.114343
Nerea Lorenzo-Parodi , Susanne Moebus , Torsten C. Schmidt
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Abstract

Several aromatic amines (AA) are classified as human carcinogens, and tobacco smoke is one of the main sources of exposure. Once in the human body, they undergo different metabolic pathways which lead to either their excretion or ultimately to the formation of DNA and protein adducts.

The aim of this study was to investigate AA in 68 urine samples (aged 29–79, 47% female), including 10 smokers (S), 28 past-smokers (PS) and 30 never-smokers (NS), and to study if there was a relation between the smoking status and the amount of the AA present. GCxGC-MS was used to analyze AA in complex urine samples due to its high peak capacity and the fact that it provides two sets of retention times and structural information, which facilitates the separation and identification of the target analytes.

First, a qualitative comparison of an example set of a NS, PS and S sample was carried out, in which 38, 45 and 46 AA, respectively, could be tentatively identified. Afterwards, seven AA were successfully quantified in the samples. Of these, 4-ethylaniline (4EA, p = 0.015), 2,4,6-trimethylaniline (2,4,6TMA, p = 0.030), 2-naphthylamine (2NA, p = 0.014) and the sum of 2,4- and 2,6-dimethylaniline (DMA, p = 0.017) were found in significantly different (α = 0.05) concentrations for the S, 29 ± 14, 87 ± 49, 41 ± 26, and 105 ± 57 ng/L respectively, compared to the NS, 15 ± 6, 42 ± 30, 16 ± 6, and 48 ± 28 ng/L. And 2,4,6TMA (39 ± 26, p = 0.022), 2NA (18 ± 9, p = 0.025) and DMA (53 ± 46, p = 0.030), were also found at significantly higher concentrations in samples from S when compared to PS. However, some samples had AA concentrations outside the calibration curve and could not be taken into account, especially for 2-methylaniline (2MA). Therefore, all the samples were evaluated using a quantitative screening approach, by which the intensities of 4EA (p = 0.019), 2,4,6TMA (p = 0.048), 2NA (p = 0.016), DMA (p = 0.019) and 2MA (p = 0.006) in S were found to be significantly (α = 0.05) higher than in the NS, and 2MA (p = 0.019) and 4EA (p = 0.023) in S were found to be significantly higher than in the PS. An association between the smoking status and the amount of certain AA present could therefore be found. This information could be used to study the relation between the smoking status, the amount of AA present, and smoking related diseases like bladder cancer.

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利用综合多维气相色谱-质谱法(GCxGC-MS)分析人体尿液中的芳香胺类化合物
几种芳香胺(AA)被归类为人类致癌物,而烟草烟雾是接触芳香胺的主要来源之一。本研究旨在调查 68 份尿液样本(年龄在 29-79 岁之间,47% 为女性)中的 AA 含量,其中包括 10 名吸烟者(S)、28 名既往吸烟者(PS)和 30 名从不吸烟者(NS),并研究吸烟状况与 AA 含量之间是否存在关系。GCxGC-MS 用于分析复杂尿样中的 AA,因为它的峰容量大,而且能提供两组保留时间和结构信息,有利于目标分析物的分离和鉴定。随后,样品中的七种 AA 被成功定量。其中,4-乙基苯胺(4EA,p = 0.015)、2,4,6-三甲基苯胺(2,4,6TMA,p = 0.030)、2-萘胺(2NA,p = 0.014)以及 2,4-和 2,6-二甲基苯胺的总和(DMA,p = 0.017),与 NS(15±6、42±30、16±6 和 48±28 ng/L)相比,S 的浓度明显不同(α = 0.05),分别为 29±14、87±49、41±26 和 105±57 ng/L。与 PS 样本相比,S 样本中 2,4,6TMA(39 ± 26,p = 0.022)、2NA(18 ± 9,p = 0.025)和 DMA(53 ± 46,p = 0.030)的浓度也明显较高。不过,有些样品中的 AA 浓度超出了校准曲线的范围,因此无法将其考虑在内,尤其是 2-甲基苯胺(2MA)。因此,我们采用定量筛选法对所有样品进行了评估,其中 4EA(p = 0.019)、2,4,6TMA(p = 0.048)、2NA(p = 0.016)、DMA(p = 0.结果发现,S 组中的 2MA (p = 0.019) 和 4EA (p = 0.023) 明显高于 PS 组。因此,可以发现吸烟状况与某些 AA 的含量之间存在关联。这些信息可用于研究吸烟状况、AA 含量与膀胱癌等与吸烟有关的疾病之间的关系。
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来源期刊
CiteScore
11.50
自引率
5.00%
发文量
151
审稿时长
22 days
期刊介绍: The International Journal of Hygiene and Environmental Health serves as a multidisciplinary forum for original reports on exposure assessment and the reactions to and consequences of human exposure to the biological, chemical, and physical environment. Research reports, short communications, reviews, scientific comments, technical notes, and editorials will be peer-reviewed before acceptance for publication. Priority will be given to articles on epidemiological aspects of environmental toxicology, health risk assessments, susceptible (sub) populations, sanitation and clean water, human biomonitoring, environmental medicine, and public health aspects of exposure-related outcomes.
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