利用常压氨加成电离质谱法灵敏测定挥发性亚硝胺。

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Analytical and Bioanalytical Chemistry Pub Date : 2024-12-01 Epub Date: 2024-10-14 DOI:10.1007/s00216-024-05580-7
Lian Duan, Cheng Wang, Yuwei Li, Binwang Yang, Xiuqing Zheng, Jiaxu Liu, Guoxing Jing, Wenjie Liu, Jianna Yu
{"title":"利用常压氨加成电离质谱法灵敏测定挥发性亚硝胺。","authors":"Lian Duan, Cheng Wang, Yuwei Li, Binwang Yang, Xiuqing Zheng, Jiaxu Liu, Guoxing Jing, Wenjie Liu, Jianna Yu","doi":"10.1007/s00216-024-05580-7","DOIUrl":null,"url":null,"abstract":"<p><p>In recent years, the control of volatile N-nitrosamines (NAs) has been of interest in the pharmaceutical and food industries, as many of these compounds are probable human carcinogens. Thus, rapid and trace-level quantitative determination methods are in urgent demand. In this work, ambient pressure ammonium-adduct ionization mass spectrometry was proposed for the sensitive detection of volatile nitrosamines in various pharmaceutical headspaces. The ammonium ions produced through electrospray ionization acted as reactant ions for NAs to generate ammonium-NA adduct ions and underwent in-source collision-induced dissociation to produce protonated NAs, which were detected by mass spectrometry. The ionization selectivity and sensitivity for various volatile NAs were improved significantly using the developed method, which was demonstrated by the limit of quantification (LOQ) below 52 ng L<sup>-1</sup> for all NAs, and the quantitative performance was consequently improved. Different NAs exhibited almost equimolar response using NH<sub>4</sub><sup>+</sup> as the reactant ion, with at least a twofold enhancement in intensity for the individual compounds relative to when using H<sup>+</sup> as the reactant ion. The proposed method is a rapid, sensitive, and environmentally economical approach that uses few reagents.</p>","PeriodicalId":462,"journal":{"name":"Analytical and Bioanalytical Chemistry","volume":" ","pages":"6839-6847"},"PeriodicalIF":3.8000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sensitive determination of volatile nitrosamines with ambient pressure ammonium-adduct ionization mass spectrometry.\",\"authors\":\"Lian Duan, Cheng Wang, Yuwei Li, Binwang Yang, Xiuqing Zheng, Jiaxu Liu, Guoxing Jing, Wenjie Liu, Jianna Yu\",\"doi\":\"10.1007/s00216-024-05580-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In recent years, the control of volatile N-nitrosamines (NAs) has been of interest in the pharmaceutical and food industries, as many of these compounds are probable human carcinogens. Thus, rapid and trace-level quantitative determination methods are in urgent demand. In this work, ambient pressure ammonium-adduct ionization mass spectrometry was proposed for the sensitive detection of volatile nitrosamines in various pharmaceutical headspaces. The ammonium ions produced through electrospray ionization acted as reactant ions for NAs to generate ammonium-NA adduct ions and underwent in-source collision-induced dissociation to produce protonated NAs, which were detected by mass spectrometry. The ionization selectivity and sensitivity for various volatile NAs were improved significantly using the developed method, which was demonstrated by the limit of quantification (LOQ) below 52 ng L<sup>-1</sup> for all NAs, and the quantitative performance was consequently improved. Different NAs exhibited almost equimolar response using NH<sub>4</sub><sup>+</sup> as the reactant ion, with at least a twofold enhancement in intensity for the individual compounds relative to when using H<sup>+</sup> as the reactant ion. The proposed method is a rapid, sensitive, and environmentally economical approach that uses few reagents.</p>\",\"PeriodicalId\":462,\"journal\":{\"name\":\"Analytical and Bioanalytical Chemistry\",\"volume\":\" \",\"pages\":\"6839-6847\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical and Bioanalytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s00216-024-05580-7\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical and Bioanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s00216-024-05580-7","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

近年来,对挥发性 N-亚硝胺(NAs)的控制一直受到制药和食品行业的关注,因为其中许多化合物可能是人类致癌物质。因此,迫切需要快速、痕量的定量测定方法。在这项工作中,我们提出了常压铵加成电离质谱法,用于灵敏检测各种药剂顶层空间中的挥发性亚硝胺。电喷雾离子化产生的铵离子作为亚硝胺的反应离子,生成铵-亚硝胺加成离子,经过源内碰撞诱导解离生成质子化的亚硝胺,并通过质谱进行检测。该方法对各种挥发性NA的电离选择性和灵敏度均有显著提高,所有NA的定量限(LOQ)均低于52 ng L-1,从而提高了定量性能。以 NH4+ 作为反应离子时,不同的 NAs 几乎呈等摩尔反应,与以 H+ 作为反应离子时相比,单个化合物的强度至少提高了两倍。所提出的方法是一种快速、灵敏且环保经济的方法,只需使用少量试剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sensitive determination of volatile nitrosamines with ambient pressure ammonium-adduct ionization mass spectrometry.

In recent years, the control of volatile N-nitrosamines (NAs) has been of interest in the pharmaceutical and food industries, as many of these compounds are probable human carcinogens. Thus, rapid and trace-level quantitative determination methods are in urgent demand. In this work, ambient pressure ammonium-adduct ionization mass spectrometry was proposed for the sensitive detection of volatile nitrosamines in various pharmaceutical headspaces. The ammonium ions produced through electrospray ionization acted as reactant ions for NAs to generate ammonium-NA adduct ions and underwent in-source collision-induced dissociation to produce protonated NAs, which were detected by mass spectrometry. The ionization selectivity and sensitivity for various volatile NAs were improved significantly using the developed method, which was demonstrated by the limit of quantification (LOQ) below 52 ng L-1 for all NAs, and the quantitative performance was consequently improved. Different NAs exhibited almost equimolar response using NH4+ as the reactant ion, with at least a twofold enhancement in intensity for the individual compounds relative to when using H+ as the reactant ion. The proposed method is a rapid, sensitive, and environmentally economical approach that uses few reagents.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信