利用氢气作为载气和改进的离子源,开发了一种新型、绿色、高效和环保的 GC-MS/MS 分析方法,用于可靠、快速地测定 dl-PCBs 和 PCDD/Fs。

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Talanta Pub Date : 2025-02-01 Epub Date: 2024-11-07 DOI:10.1016/j.talanta.2024.127180
Kartal Çetintürk, Barış Güzel, Oltan Canlı
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引用次数: 0

摘要

多氯二苯并对二恶英/呋喃(PCDD/Fs)和二恶英类多氯联苯(dl-PCBs)是一种全球性污染物,它们往往会在多种基质中累积。因此,由于它们的累积率最高且具有顽固性,对它们的精确定量会对人类和生物产生重大的毒理影响。这项研究的目的是,在气相色谱-三重四极杆(GC-MS/MS)系统中使用氢气而不是氦气,有助于改进对环境基质中 dl-PCBs 和 PCDD/Fs 的分析。该研究评估了多氯二苯并对二恶英和多氯二苯并呋喃分析所需的色谱分辨率标准下的分析时间性能,监测了可信的质谱/碎片比变化,并最终确定了目标最毒持久性有机化合物同系物的定量限。使用 H2 载气的主要优点是分析时间大大缩短(2.5 倍),同时由于峰宽增加了 0.6-0.7 倍,分辨率也得到了提高。这项研究强调,多氯二苯并对二恶英和多氯二苯并呋喃的六同系物对分辨率有显著影响;几乎可以观察到基线分离。不过,灵敏度略有降低(6-7 倍),这影响了校准起始浓度(0.8-3.2 pg/μl)。获得的质谱显示,较低的片段增强效果明显,尤其是氯化程度较高的同系物(六、七和八同系物)。本研究中计算出的正交效应值(1-58)与之前文献中的结果(1-66 和 1-83)一致,并支持观察到的较低片段增强的结论。尽管未检测到氢化现象,但所研究的化合物在氦气和氢气载气中的量子/质子比值存在显著差异。对最终确定的方法进行了检验,并在为期三个月的实际样品分析中对 hydroinert® 离子源的性能进行了评估(RSD ≤17.8%)。结果表明,氢气在环境基质的 dl-PCBs 和 PCDD/Fs 中是一种潜在可靠的 GC-MS/MS 载气。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The development of a novel, green, efficient, and eco-friendly GC-MS/MS analytical method for the reliable and rapid determination of dl-PCBs, and PCDD/Fs using hydrogen as a carrier gas and a modified ion source.

The polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (dl-PCBs) are worldwide contaminants, and they tend to accumulate in wide variety of matrices. Therefore, due to the highest accumulation rate and recalcitrancy, their precise quantification makes significant concern about their toxicological effects on both humans and organisms. The objective of the study is that using hydrogen carrier gas instead of helium in gas chromatography with triple quadrupole (GC-MS/MS) systems could contribute to improvements on the analysis of dl-PCBs and PCDD/Fs in environmental matrices. The study evaluates the performance of the analysis time under the desired chromatographic resolution criteria for PCDD/Fs analysis, monitoring the plausible mass spectrum/fragmentation ratio changes, and finally the quantification limits of the targeted most toxic persistent organic compound congeners. The main advantage of using H2 carrier gas is that the analysis time was drastically reduced (∼2.5 times) along with improved resolution due to an increase in peak widths in ∼0.6-0.7 factor. This study emphasized that the resolution was remarkably affected by the hexa congeners of PCDD/Fs; nearly baseline separation was observed. However, the sensitivity was slightly reduced (∼6-7 fold), which affected the calibration starting concentrations (0.8-3.2 pg/μl). The acquired mass spectra indicated that the lower fragment enhancement was noticeable, particularly on higher chlorinated ones (hexa, hepta, and octa congeners). The calculated ortho-effect values (1-58) in this study are consistent with the previous results in the literature (1-66 and 1-83) and supports the conclusion about the observations of lower fragment enhancement. Despite non-detection of hydrogenation, there is a significant difference in the quant/qual ion ratios in the studied compounds between helium and hydrogen carrier gas. The finalized methodology was examined, and the performance of the hydroinert® ion source was assessed over a three-month analysis period with a real sample analysis (RSD ≤17.8 %). The results indicate that hydrogen is a potential and reliable GC-MS/MS carrier gas in dl-PCBs and PCDD/Fs for environmental matrices.

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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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