固体支撑液-液萃取-超高效液相色谱-串联质谱法测定人尿中17种双酚类化合物

Yu'e Jin, Lan-Ge Zhang, Jing-Xian Zhou, Jin-Jing Ma, Li-Li Yuan, Ping Xiao, Guo-Quan Wang
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引用次数: 0

摘要

双酚A (BPA)及其类似物统称为双酚化合物(bp),主要用于聚碳酸酯塑料和环氧树脂的制造。bp普遍存在于各种环境基质、人体组织和代谢产物中。大量研究表明bp对神经系统、生殖系统、免疫系统和代谢系统都有不利影响。人体接触后,bp主要通过尿液排出。因此,开发有效和可靠的尿液bp定量分析方法对于评估人群暴露水平至关重要。本研究将固支液液萃取(SLE)与超高效液相色谱-串联质谱(UHPLC-MS/MS)技术相结合,建立了人体尿液中17种BPs的高通量测定方法。样品经酶解处理后,依次进行全自动SLE纯化、吹氮浓缩、再溶等步骤。采用CAPCELL PAK ADME色谱柱(100 mm×2.1 mm, 2 μm)分离,以0.05 mmol/L氟化铵水溶液和0.05 mmol/L氟化铵甲醇溶液为流动相进行梯度洗脱。在多反应监测(MRM)模式下,采用电喷雾电离(ESI)负离子扫描模式进行质谱检测。采用保留时间和离子丰度比进行定性分析,采用内标法进行定量分析。在优化条件下,可有效分离17个bp。17种BPs在相应的质量浓度范围内线性关系良好,相关系数(r)≥0.998 6,检出限(lod)为0.002 ~ 0.489 μg/L,定量限(LOQ)为0.005 ~ 0.986 μg/L。选取背景含量较低的儿童混合尿样作为基质,在低、中、高三个加标水平下进行加标回收率试验。结果表明,17种bp的加样回收率为61.1% ~ 121.7%,日内rsd为1.3% ~ 11.2%,日内rsd为3.7% ~ 19.0%。采用该方法对50份随机尿样进行检测,结果显示共检测出11种bp。其中双酚S (BPS)和BPA的检出率最高,分别为98.0%和86.0%,中位检出量分别为0.075 μg/L和0.829 μg/L。该方法操作简便、灵敏度高、可靠。适用于人体尿液中17种bp的快速定量分析,可为人群bp暴露风险评估提供有效的技术支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Determination of 17 bisphenol compounds in human urine by solid supported liquid-liquid extraction-ultra-high performance liquid chromatography-tandem mass spectrometry].

[Determination of 17 bisphenol compounds in human urine by solid supported liquid-liquid extraction-ultra-high performance liquid chromatography-tandem mass spectrometry].

[Determination of 17 bisphenol compounds in human urine by solid supported liquid-liquid extraction-ultra-high performance liquid chromatography-tandem mass spectrometry].

Bisphenol A (BPA) and its analogs are collectively termed bisphenol compounds (BPs), which are predominantly utilized in the manufacturing of polycarbonate plastics and epoxy resins. BPs are ubiquitous in diverse environmental matrices, human tissues, and metabolic products. Extensive research has demonstrated that BPs exert adverse effects on the nervous, reproductive, immune, and metabolic systems. After exposure in humans, BPs are primarily excreted in urine. Consequently, the development of efficient and robust analytical methods for BPs quantification in urine is essential for assessing population exposure levels. In this study, solid supported liquid-liquid extraction (SLE) was combined with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) technology to establish a high-throughput determination method for 17 BPs in human urine. After enzymatic hydrolysis treatment of the samples, the steps of fully automatic SLE purification, nitrogen blowing concentration and redissolution were carried out successively. Separation was performed using a CAPCELL PAK ADME chromatography column (100 mm×2.1 mm, 2 μm), and gradient elution was carried out with 0.05 mmol/L ammonium fluoride aqueous solution and 0.05 mmol/L ammonium fluoride methanol solution as the mobile phases. MS detection was carried out using the electrospray ionization (ESI) negative ion scanning mode under the multi-reaction monitoring (MRM) mode. Qualitative analysis was conducted based on retention time and ion abundance ratio, and quantitative analysis was performed using the internal standard method. Under the optimized conditions, 17 BPs can be effectively separated. The linear relationships of the 17 BPs within the corresponding mass concentration ranges were good, and the correlation coefficients (r) were ≥0.998 6, the limits of detection (LODs) and quantification (LOQ) were 0.002-0.489 μg/L and 0.005-0.986 μg/L, respectively. Children's mixed urine samples with low background content were selected as the matrix, and then spiked recovery tests were conducted at three spiked levels (low, medium and high). The results showed that the recoveries of 17 BPs were 61.1%-121.7%, the intra-day RSDs were 1.3%-11.2%, and the inter-day RSDs were 3.7%-19.0%. This method was used to determine 50 random urine samples, and the results showed that a total of 11 BPs were detected. Among them, bisphenol S (BPS) and BPA had the highest detection rates, which were 98.0% and 86.0% respectively, and the median detection levels were 0.075 μg/L and 0.829 μg/L respectively. This method is simple to operate, sensitive and reliable. It is suitable for the rapid quantitative analysis of 17 BPs in human urine and can provide effective technical support for the risk assessment of BPs exposure in the population.

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