Application of Uplc/Ms/Ms Method for Dertermination of Sudan I in Chili Sauces

Nguyen Kieu Hung, Truong Quang Hien, Tran Ngoc Hien, Nguyen Thi Thuy Linh, Nguyen Thi Ha
{"title":"Application of Uplc/Ms/Ms Method for Dertermination of Sudan I in Chili Sauces","authors":"Nguyen Kieu Hung, Truong Quang Hien, Tran Ngoc Hien, Nguyen Thi Thuy Linh, Nguyen Thi Ha","doi":"10.25073/2588-1094/vnuees.4963","DOIUrl":null,"url":null,"abstract":"This study was carried out to verify and evaluate a method to quantify the relative Sudan I color product using ultra-high performance liquid chromatography coupled with tandem massspectrometry (UPLC/MS/MS). Sudan I was extracted through an Oasis HLB 3cc Vac Cartridge solid phase extraction column 60 mg, after that quantified by UPLC/MS/MS. The program uses a C18 column (2.1 x 100 mm, 1.7 µm), the mobile phase is acetonitrile and water containing 0.1% formic acid, the flow rate is 0.4 ml/min. Running conditions of MRM (Multiple Reaction Monitoring) mode, select molecular ion fragment 249 amu. The verification results have good linearity, the limit of detection (LOD) and the limit of quantification (LOQ) of the analytical procedure are 1.17 and 3.72 ng/g, respectively. The Sudan I recovery efficiency ranged from 82.00-107.33% with the relative standard deviation (RSD) between 4.35-9.04%. Highly sensitive sample extraction procedure is suitable for the determination of Sudan I in food based on 4 ionic fragments characteristics, meeting the requirements of the decision 2002/657/EC of the common European community. The verified analytical procedure was applied to quantitatively identify Sudan I in 21 chili samples. The results showed that Sudan I was not detected in all analyzed samples. The analytical procedure of Sudan I in this study could be used for food safety testing. \n  \n  \n ","PeriodicalId":247618,"journal":{"name":"VNU Journal of Science: Earth and Environmental Sciences","volume":"44 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"VNU Journal of Science: Earth and Environmental Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25073/2588-1094/vnuees.4963","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This study was carried out to verify and evaluate a method to quantify the relative Sudan I color product using ultra-high performance liquid chromatography coupled with tandem massspectrometry (UPLC/MS/MS). Sudan I was extracted through an Oasis HLB 3cc Vac Cartridge solid phase extraction column 60 mg, after that quantified by UPLC/MS/MS. The program uses a C18 column (2.1 x 100 mm, 1.7 µm), the mobile phase is acetonitrile and water containing 0.1% formic acid, the flow rate is 0.4 ml/min. Running conditions of MRM (Multiple Reaction Monitoring) mode, select molecular ion fragment 249 amu. The verification results have good linearity, the limit of detection (LOD) and the limit of quantification (LOQ) of the analytical procedure are 1.17 and 3.72 ng/g, respectively. The Sudan I recovery efficiency ranged from 82.00-107.33% with the relative standard deviation (RSD) between 4.35-9.04%. Highly sensitive sample extraction procedure is suitable for the determination of Sudan I in food based on 4 ionic fragments characteristics, meeting the requirements of the decision 2002/657/EC of the common European community. The verified analytical procedure was applied to quantitatively identify Sudan I in 21 chili samples. The results showed that Sudan I was not detected in all analyzed samples. The analytical procedure of Sudan I in this study could be used for food safety testing.      
Uplc/Ms/Ms法测定辣椒酱中苏丹红I的应用
本研究验证和评价了超高效液相色谱-串联质谱(UPLC/MS/MS)定量苏丹红I色相关产物的方法。用Oasis HLB 3cc Vac Cartridge固相萃取柱提取苏丹红I型60 mg,经UPLC/MS/MS定量。程序采用C18色谱柱(2.1 × 100 mm, 1.7µm),流动相为乙腈和含0.1%甲酸的水,流速0.4 ml/min。多反应监测(MRM)模式运行条件,选择分子离子片段249 amu。验证结果线性良好,分析方法的检出限和定量限分别为1.17和3.72 ng/g。苏丹红1号的回收率为82.00 ~ 107.33%,相对标准偏差(RSD)为4.35 ~ 9.04%。基于4个离子片段特征的高灵敏度样品提取方法适用于食品中苏丹酸的测定,符合欧共体第2002/657/EC号决议的要求。应用验证的分析方法对21份辣椒样品中的苏丹红I进行了定量鉴定。结果表明,在所有分析样品中均未检测到苏丹I。本研究的苏丹红1号分析方法可用于食品安全检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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