Development, optimisation, and pre-validation of a gas chromatography—Ion mobility spectrometry method with preliminary twofold enrichment for the sensitive detection of NNitrosamines in drinking water

IF 3.2
Jana Hinz , Kaliyani Wickneswaran , Ursula Telgheder , Michaela Wirtz
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Abstract

NNitrosamines have long been identified as a relevant contaminant in potable water due to their identification as probable human carcinogens. Thus, highly sensitive detection of these pollutants in the ultra-trace range is imperative to comply with strict regulatory specifications. To this end, many institutions rely on mass spectrometry-based analysis methods, which have the disadvantage of being cost- and resource intensive. This study aims to develop, optimise, and evaluate a gas chromatography-drift tube-ion mobility spectrometry (GC-IMS) based method with a twofold enrichment strategy consisting of solid phase extraction (SPE) followed by in-tube extraction (ITEX) of the eluate for nine different nitrosamines in drinking water in order to offer a sensitive alternative to the current state of the art. Optimisation of ITEX parameters was successfully performed using a simplex self-directing design approach, so that a calibration range between 5 and 50 ng/L could be achieved. The suitability of a linear regression model was demonstrated via analysis of variance (ANOVA) criteria. The analysis of different spiked drinking water samples allowed for the determination of the method’s accuracy (27.3 – 114.5 % across different nitrosamine analytes and matrices, with most above 70 % recovery) and detection limits (1.12 – 12.48 ng/L across different nitrosamine analytes and matrices), which fall within the range of required limit values. Tested drinking waters show innate nitrosamine concentrations well below detection limits and can thus be deemed free from contaminants.

Abstract Image

气相色谱-离子迁移率光谱法的建立、优化和预验证,用于饮用水中亚硝胺的灵敏检测
长期以来,亚硝胺一直被认为是饮用水中的一种相关污染物,因为它们被认为是可能的人类致癌物。因此,在超痕量范围内对这些污染物进行高灵敏度检测是必须遵守严格的监管规范的。为此,许多机构依靠基于质谱的分析方法,其缺点是成本和资源密集。本研究旨在开发、优化和评估一种基于气相色谱-漂移管离子迁移谱法(GC-IMS)的方法,该方法采用双重富集策略,包括固相萃取(SPE)和管内萃取(ITEX)对饮用水中9种不同亚硝胺的洗脱液进行富集,以提供一种灵敏的替代方法。使用简单的自导向设计方法成功地对ITEX参数进行了优化,因此可以实现5至50 ng/L的校准范围。通过方差分析(ANOVA)标准证明了线性回归模型的适用性。通过对不同加标饮用水样品的分析,可以确定该方法的准确度(在不同亚硝胺分析物和基质中为27.3 - 114.5%,回收率大多在70%以上)和检出限(在不同亚硝胺分析物和基质中为1.12 - 12.48 ng/L),均在要求的极限值范围内。经检测的饮用水显示,天然亚硝胺浓度远低于检测限度,因此可以认为不含污染物。
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来源期刊
Journal of chromatography open
Journal of chromatography open Analytical Chemistry
CiteScore
2.50
自引率
0.00%
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50 days
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