PRiME HLB净化联合超高效液相色谱-串联质谱法同时测定大豆制品中的10种甜味剂。

IF 2.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Yi Bao, Jinping Guo, Jinming Wang, Dan Li, Zhuo Lv, Xu Zhang, Xue Yang, Zeyue Gao and Lanying Zhou
{"title":"PRiME HLB净化联合超高效液相色谱-串联质谱法同时测定大豆制品中的10种甜味剂。","authors":"Yi Bao, Jinping Guo, Jinming Wang, Dan Li, Zhuo Lv, Xu Zhang, Xue Yang, Zeyue Gao and Lanying Zhou","doi":"10.1039/D5AY00897B","DOIUrl":null,"url":null,"abstract":"<p >A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (<em>m</em>-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using <em>n</em>-hexane liquid–liquid extraction and purified by solid phase extraction using an <em>m</em>-PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C<small><sub>18</sub></small> (2.1 mm × 150 mm, 1.7 μm) column, and gradient eluted with a mixed solution of (5 mmol L<small><sup>−1</sup></small> ammonium formate +0.1% formic acid) and acetonitrile. The mass spectrometric acquisition was performed by multiple-reaction monitoring (MRM) in both negative and positive ionization mode. Quantitative analysis was performed using an external standard method with matrix-matched calibration curves. Under optimal conditions, a total of ten target compounds were well separated within 10 min, and a good linearity was obtained in the concentration range of 5.00–500 μg L<small><sup>−1</sup></small> with correlation coefficients greater than 0.99, and the limits of detection (LODs) and quantification (LOQs) for ACE-K, SAC and SCL were 25.0 and 50.0 μg kg<small><sup>−1</sup></small>; the limits of detection (LODs) and quantification (LOQs) for CYC, ASP, ALI, RBA, STV, ADV and NEO were 12.5 and 25.0 μg kg<small><sup>−1</sup></small>,respectively. The recoveries of the ten sweeteners in soymilk samples ranged from 76.9% to 115% at low, medium and high spiked levels (25.0–50.0 μg kg<small><sup>−1</sup></small>, 50.0–100 μg kg<small><sup>−1</sup></small>, and 250–500 μg kg<small><sup>−1</sup></small>), with precisions (RSD) in the range of 0.62–3.98%. This method is simple, rapid, accurate and sensitive, which greatly improves the efficiency of sample analysis and the accuracy of qualitative and quantitative analysis results of the target substances. It could meet the needs of quantitative analysis and qualitative screening of sweeteners in bulk soybean product samples, and provide technical support for rapid analysis of sweeteners in soybean products. It is of great significance for the analysis of trace components of sweeteners in soybean products.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" 37","pages":" 7482-7490"},"PeriodicalIF":2.6000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simultaneous determination of ten sweeteners in soybean products using PRiME HLB purification combined with ultra-high-performance liquid chromatography-tandem mass spectrometry\",\"authors\":\"Yi Bao, Jinping Guo, Jinming Wang, Dan Li, Zhuo Lv, Xu Zhang, Xue Yang, Zeyue Gao and Lanying Zhou\",\"doi\":\"10.1039/D5AY00897B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (<em>m</em>-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using <em>n</em>-hexane liquid–liquid extraction and purified by solid phase extraction using an <em>m</em>-PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C<small><sub>18</sub></small> (2.1 mm × 150 mm, 1.7 μm) column, and gradient eluted with a mixed solution of (5 mmol L<small><sup>−1</sup></small> ammonium formate +0.1% formic acid) and acetonitrile. The mass spectrometric acquisition was performed by multiple-reaction monitoring (MRM) in both negative and positive ionization mode. Quantitative analysis was performed using an external standard method with matrix-matched calibration curves. Under optimal conditions, a total of ten target compounds were well separated within 10 min, and a good linearity was obtained in the concentration range of 5.00–500 μg L<small><sup>−1</sup></small> with correlation coefficients greater than 0.99, and the limits of detection (LODs) and quantification (LOQs) for ACE-K, SAC and SCL were 25.0 and 50.0 μg kg<small><sup>−1</sup></small>; the limits of detection (LODs) and quantification (LOQs) for CYC, ASP, ALI, RBA, STV, ADV and NEO were 12.5 and 25.0 μg kg<small><sup>−1</sup></small>,respectively. The recoveries of the ten sweeteners in soymilk samples ranged from 76.9% to 115% at low, medium and high spiked levels (25.0–50.0 μg kg<small><sup>−1</sup></small>, 50.0–100 μg kg<small><sup>−1</sup></small>, and 250–500 μg kg<small><sup>−1</sup></small>), with precisions (RSD) in the range of 0.62–3.98%. This method is simple, rapid, accurate and sensitive, which greatly improves the efficiency of sample analysis and the accuracy of qualitative and quantitative analysis results of the target substances. It could meet the needs of quantitative analysis and qualitative screening of sweeteners in bulk soybean product samples, and provide technical support for rapid analysis of sweeteners in soybean products. It is of great significance for the analysis of trace components of sweeteners in soybean products.</p>\",\"PeriodicalId\":64,\"journal\":{\"name\":\"Analytical Methods\",\"volume\":\" 37\",\"pages\":\" 7482-7490\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Methods\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ay/d5ay00897b\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Methods","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ay/d5ay00897b","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

建立了多塞过滤净化(m-PFC)联合超高效液相色谱-串联质谱(UPLC-MS/MS)测定大豆制品中10种甜味剂的方法。样品用乙腈(含1%甲酸)提取,正己烷液液萃取脱脂,m-PFC柱(Oasis PRiME HLB)固相萃取纯化。采用Waters ACQUITY UPLC®BEH C18 (2.1 mm × 150 mm, 1.7 μm)色谱柱分离,用(5 mmol L-1甲酸铵+0.1%甲酸)和乙腈混合溶液梯度洗脱。质谱采集是通过多反应监测(MRM)在负离子和正离子模式下进行的。采用矩阵匹配校准曲线的外标法进行定量分析。在最佳条件下,10个目标化合物在10 min内分离效果良好,在5.00 ~ 500 μg -1范围内线性良好,相关系数大于0.99,ACE-K、SAC和SCL的检出限(lod)和定量限(loq)分别为25.0和50.0 μg -1;CYC、ASP、ALI、RBA、STV、ADV和NEO的检出限(lod)和定量限(loq)分别为12.5和25.0 μ kg-1。在低、中、高加标水平(25.0 ~ 50.0 μg kg-1、50.0 ~ 100 μg kg-1和250 ~ 500 μg kg-1)下,10种甜味剂的加标回收率为76.9% ~ 115%,精密度(RSD)为0.62 ~ 3.98%。该方法简便、快速、准确、灵敏,大大提高了样品分析效率和目标物质定性、定量分析结果的准确性。该方法可满足大宗豆制品中甜味剂定量分析和定性筛选的需要,为豆制品中甜味剂的快速分析提供技术支持。这对大豆制品中甜味剂微量成分的分析具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Simultaneous determination of ten sweeteners in soybean products using PRiME HLB purification combined with ultra-high-performance liquid chromatography-tandem mass spectrometry

Simultaneous determination of ten sweeteners in soybean products using PRiME HLB purification combined with ultra-high-performance liquid chromatography-tandem mass spectrometry

A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (m-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using n-hexane liquid–liquid extraction and purified by solid phase extraction using an m-PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C18 (2.1 mm × 150 mm, 1.7 μm) column, and gradient eluted with a mixed solution of (5 mmol L−1 ammonium formate +0.1% formic acid) and acetonitrile. The mass spectrometric acquisition was performed by multiple-reaction monitoring (MRM) in both negative and positive ionization mode. Quantitative analysis was performed using an external standard method with matrix-matched calibration curves. Under optimal conditions, a total of ten target compounds were well separated within 10 min, and a good linearity was obtained in the concentration range of 5.00–500 μg L−1 with correlation coefficients greater than 0.99, and the limits of detection (LODs) and quantification (LOQs) for ACE-K, SAC and SCL were 25.0 and 50.0 μg kg−1; the limits of detection (LODs) and quantification (LOQs) for CYC, ASP, ALI, RBA, STV, ADV and NEO were 12.5 and 25.0 μg kg−1,respectively. The recoveries of the ten sweeteners in soymilk samples ranged from 76.9% to 115% at low, medium and high spiked levels (25.0–50.0 μg kg−1, 50.0–100 μg kg−1, and 250–500 μg kg−1), with precisions (RSD) in the range of 0.62–3.98%. This method is simple, rapid, accurate and sensitive, which greatly improves the efficiency of sample analysis and the accuracy of qualitative and quantitative analysis results of the target substances. It could meet the needs of quantitative analysis and qualitative screening of sweeteners in bulk soybean product samples, and provide technical support for rapid analysis of sweeteners in soybean products. It is of great significance for the analysis of trace components of sweeteners in soybean products.

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
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
×
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:604180095
Book学术官方微信