A novel deep eutectic solvent based on oleic acid and betaine hydrochloride for liquid-phase microextraction of Sudan IV from water and food samples

IF 2.3 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Mustafa Soylak, Ayşe Nur Çoban, Hassan Elzain Hassan Ahmed
{"title":"A novel deep eutectic solvent based on oleic acid and betaine hydrochloride for liquid-phase microextraction of Sudan IV from water and food samples","authors":"Mustafa Soylak,&nbsp;Ayşe Nur Çoban,&nbsp;Hassan Elzain Hassan Ahmed","doi":"10.1007/s13738-025-03212-0","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, a novel green hydrophobic deep eutectic solvent (DES) composed of oleic acid (OLC) and betaine hydrochloride (BET) was synthesized and applied for the extraction of Sudan IV dye from natural water and food samples using ultrasonic-assisted dispersive liquid-phase microextraction (UA-DLPME). In this DES system, OLC acted as the hydrogen bond donor (HBD), while BET served as the hydrogen bond acceptor (HBA). Key analytical parameters, including pH, DES molar ratio, sonication and centrifugation times, and initial and final sample volumes, were studied and optimized. The DES-UA-DLPME method exhibited a rapid and efficient extraction process, achieving equilibrium within 1 min at room temperature. The method demonstrated excellent analytical performance with a limit of detection (LOD) and limit of quantification (LOQ) of 0.75 and 2.48 µg kg<sup>−1</sup> for food samples and 0.914 and 3.047 µg L<sup>−1</sup> for water samples, respectively. The method’s preconcentration factor (PF) and enrichment factor (EF) were 40 and 35.8, respectively, with an acceptable analytical recovery (AR) of 87–104% across various matrices. The linear dynamic range (LDR) was 0.1–600 µg L<sup>−1</sup> with a correlation coefficient (<i>R</i><sup>2</sup>) of 0.995. The precision of the method, expressed as relative standard deviation (RSD), was 4.9% (<i>n</i> = 6). Matrix effects were also studied and found to be negligible for the tested natural water and food samples in the recovery range of 87–106%. This DES-UA-DLPME approach offers a green, rapid, and highly effective method for the determination of Sudan IV dye in complex matrices.</p></div>","PeriodicalId":676,"journal":{"name":"Journal of the Iranian Chemical Society","volume":"22 5","pages":"1125 - 1137"},"PeriodicalIF":2.3000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s13738-025-03212-0.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Iranian Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s13738-025-03212-0","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, a novel green hydrophobic deep eutectic solvent (DES) composed of oleic acid (OLC) and betaine hydrochloride (BET) was synthesized and applied for the extraction of Sudan IV dye from natural water and food samples using ultrasonic-assisted dispersive liquid-phase microextraction (UA-DLPME). In this DES system, OLC acted as the hydrogen bond donor (HBD), while BET served as the hydrogen bond acceptor (HBA). Key analytical parameters, including pH, DES molar ratio, sonication and centrifugation times, and initial and final sample volumes, were studied and optimized. The DES-UA-DLPME method exhibited a rapid and efficient extraction process, achieving equilibrium within 1 min at room temperature. The method demonstrated excellent analytical performance with a limit of detection (LOD) and limit of quantification (LOQ) of 0.75 and 2.48 µg kg−1 for food samples and 0.914 and 3.047 µg L−1 for water samples, respectively. The method’s preconcentration factor (PF) and enrichment factor (EF) were 40 and 35.8, respectively, with an acceptable analytical recovery (AR) of 87–104% across various matrices. The linear dynamic range (LDR) was 0.1–600 µg L−1 with a correlation coefficient (R2) of 0.995. The precision of the method, expressed as relative standard deviation (RSD), was 4.9% (n = 6). Matrix effects were also studied and found to be negligible for the tested natural water and food samples in the recovery range of 87–106%. This DES-UA-DLPME approach offers a green, rapid, and highly effective method for the determination of Sudan IV dye in complex matrices.

一种新型油酸-甜菜碱共晶溶剂,用于水和食品样品中苏丹红IV的液相微萃取
本研究合成了一种由油酸(OLC)和盐酸甜菜碱(BET)组成的新型绿色疏水深共晶溶剂(DES),并将其应用于超声波辅助分散液相微萃取法(UA-DLPME)从天然水和食品样品中提取苏丹红IV染料。在该DES体系中,OLC作为氢键给体(HBD), BET作为氢键受体(HBA)。研究并优化了pH、DES摩尔比、超声和离心次数、初始和最终样品体积等关键分析参数。DES-UA-DLPME提取工艺快速高效,室温下1 min即可达到平衡。该方法具有良好的分析性能,食品样品的检出限(LOD)和定量限(LOQ)分别为0.75和2.48µg kg - 1,水样样品的检出限(LOQ)分别为0.914和3.047µg L - 1。该方法的预富集因子(PF)和富集因子(EF)分别为40和35.8,在各种基质上的可接受分析回收率(AR)为87-104%。线性动态范围(LDR)为0.1 ~ 600µg L−1,相关系数(R2)为0.995。该方法的精密度为4.9% (n = 6),以相对标准偏差(RSD)表示。对天然水和食品样品的基质效应进行了研究,发现基质效应在87 ~ 106%的回收率范围内可以忽略不计。DES-UA-DLPME方法为复杂基质中苏丹IV染料的测定提供了一种绿色、快速、高效的方法。
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
CiteScore
4.40
自引率
8.30%
发文量
230
审稿时长
5.6 months
期刊介绍: JICS is an international journal covering general fields of chemistry. JICS welcomes high quality original papers in English dealing with experimental, theoretical and applied research related to all branches of chemistry. These include the fields of analytical, inorganic, organic and physical chemistry as well as the chemical biology area. Review articles discussing specific areas of chemistry of current chemical or biological importance are also published. JICS ensures visibility of your research results to a worldwide audience in science. You are kindly invited to submit your manuscript to the Editor-in-Chief or Regional Editor. All contributions in the form of original papers or short communications will be peer reviewed and published free of charge after acceptance.
×
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