Department of Pediatrics and Department of Environmental Medicine, New York University School of Medicine, New York, NY 10016, USA.
Department of Pediatrics and Department of Environmental Medicine, New York University School of Medicine, New York, NY 10016, USA; Biochemistry Department, Faculty of Science and Experimental Biochemistry Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
Sci Total Environ. 2022 Jul 20;831:154768. doi: 10.1016/j.scitotenv.2022.154768. Epub 2022 Mar 24.
Despite their known carcinogenic potential, primary aromatic amines (AAs) continue to be used in various consumer products. Human exposure to AAs is a subject of current concern. Although urinary measurements are used in the assessment of exposure, little is known about within- and between-individual temporal variability in urinary concentrations of AAs. In this study, we determined the concentrations of 30 AAs, nicotine and cotinine in 213 first morning void (FMV) urine samples collected longitudinally for over a five-week period from 15 participants residing in the Albany area of New York State, USA. Eight AAs, namely, aniline, 2-naphthylamine (2-NA), p-cresidine (p-CD), p-toluidine (p-TD), o/m-toluidine (o/m-TD), 4-chloroaniline (4-CA), 4,4'-methylenedi-o-toluidine (4,4'-MDA), and 2,6-dimethylaniline (2,6-DMA) were found in urine at a detection frequency (DF) in the range of 68-100%. Aniline and 2,6-DMA were the predominant compounds found at median concentrations of 6.0 and 3.81 ng/mL, respectively. Intraclass correlation coefficients (ICCs) of all urinary AA concentrations, except for 4-CA, showed moderate to poor predictability (ICC values ranged 0.248-0.697). Gender and ethnicity-related variations in ∑AA concentrations were significant. Spearman's correlations among AA concentrations suggested that the sources of exposure were not related to tobacco smoke. No significant correlations existed between AAs concentrations and oxidative stress biomarkers (OSBs). The estimated daily intakes of AAs calculated based on urinary concentrations were several orders of magnitude below the tolerable daily intakes.
尽管已知芳香胺(AAs)具有致癌潜力,但它们仍继续被用于各种消费品中。人类接触 AAs 是当前关注的问题。尽管尿中测量值可用于评估暴露情况,但关于 AAs 尿浓度的个体内和个体间时间变异性知之甚少。在这项研究中,我们测定了居住在美国纽约州奥尔巴尼地区的 15 名参与者在五周多的时间内收集的 213 份首次晨尿(FMV)尿液样本中 30 种 AA、尼古丁和可替宁的浓度。在尿液中检测到 8 种 AA,即苯胺、2-萘胺(2-NA)、对甲氨基酚(p-CD)、对甲苯胺(p-TD)、邻/间甲苯胺(o/m-TD)、4-氯苯胺(4-CA)、4,4'-亚甲基二邻甲苯胺(4,4'-MDA)和 2,6-二甲基苯胺(2,6-DMA),其检出频率(DF)在 68-100%范围内。苯胺和 2,6-DMA 是含量最高的两种化合物,其中位数浓度分别为 6.0 和 3.81ng/mL。除 4-CA 外,所有尿液 AA 浓度的组内相关系数(ICC)均显示出中等至较差的可预测性(ICC 值范围为 0.248-0.697)。性别和种族相关的∑AA 浓度差异具有统计学意义。AA 浓度之间的 Spearman 相关表明,暴露源与烟草烟雾无关。AA 浓度与氧化应激生物标志物(OSB)之间无显著相关性。基于尿液浓度计算的 AA 估计每日摄入量比可耐受每日摄入量低几个数量级。