开发一种使用二元溶剂的起泡辅助分散液相微萃取法,作为一种无需稀释即可同时进行萃取和预浓缩的分析葡萄汁中农药的专用方法

IF 1.3 Q4 CHEMISTRY, ANALYTICAL SEPARATION SCIENCE PLUS Pub Date : 2023-12-04 DOI:10.1002/sscp.202300195
M. Farajzadeh, Ali Hoboobi, S. Pezhhanfar, M. Mogaddam
{"title":"开发一种使用二元溶剂的起泡辅助分散液相微萃取法,作为一种无需稀释即可同时进行萃取和预浓缩的分析葡萄汁中农药的专用方法","authors":"M. Farajzadeh, Ali Hoboobi, S. Pezhhanfar, M. Mogaddam","doi":"10.1002/sscp.202300195","DOIUrl":null,"url":null,"abstract":"In this study, a swift and economical extraction and preconcentration method called effervescence‐assisted dispersive liquid‐phase microextraction was developed to analyze the pesticide content of different grape juices. To propel the microextraction method, the sample was transferred to a conical bottom glass test tube, and ammonium chloride was added and vortexed to dissolve. Then, sodium bicarbonate and a mixture of 1,2‐dibromoethane and n‐hexane were added. The tube was located in a water bath and the produced carbon dioxide bubbles dispersed the extraction solvent into the sample. Finally, it was centrifuged and one microliter of the sedimented phase was injected into a gas chromatograph equipped with a flame ionization detector. Under the optimum conditions, the limits of detection and quantification ranged from 0.9 to 4.1 and 3.0 to 13.6 μg/L, respectively. Extraction recoveries and enrichment factors were achieved in the ranges of 36%–80% and 180%–404%, respectively. The inter‐ and intra‐day relative standard deviations were in the ranges of 3.4%–10.6% and 2.6%–9.7%, respectively. Also, the coefficients of determination in the calibration curves were ≥0.990. Short extraction time, no sorbent or costly apparatuses, using inexpensive chemicals, applying microliter levels of the extractant, and no dilution of the real samples are the highlights of the study.","PeriodicalId":21639,"journal":{"name":"SEPARATION SCIENCE PLUS","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development of an effervescence‐assisted dispersive liquid phase microextraction using a binary solvent as a simultaneous extraction and preconcentration approach specialized for the analysis of pesticides in grape juice without dilution\",\"authors\":\"M. Farajzadeh, Ali Hoboobi, S. Pezhhanfar, M. Mogaddam\",\"doi\":\"10.1002/sscp.202300195\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, a swift and economical extraction and preconcentration method called effervescence‐assisted dispersive liquid‐phase microextraction was developed to analyze the pesticide content of different grape juices. To propel the microextraction method, the sample was transferred to a conical bottom glass test tube, and ammonium chloride was added and vortexed to dissolve. Then, sodium bicarbonate and a mixture of 1,2‐dibromoethane and n‐hexane were added. The tube was located in a water bath and the produced carbon dioxide bubbles dispersed the extraction solvent into the sample. Finally, it was centrifuged and one microliter of the sedimented phase was injected into a gas chromatograph equipped with a flame ionization detector. Under the optimum conditions, the limits of detection and quantification ranged from 0.9 to 4.1 and 3.0 to 13.6 μg/L, respectively. Extraction recoveries and enrichment factors were achieved in the ranges of 36%–80% and 180%–404%, respectively. The inter‐ and intra‐day relative standard deviations were in the ranges of 3.4%–10.6% and 2.6%–9.7%, respectively. Also, the coefficients of determination in the calibration curves were ≥0.990. Short extraction time, no sorbent or costly apparatuses, using inexpensive chemicals, applying microliter levels of the extractant, and no dilution of the real samples are the highlights of the study.\",\"PeriodicalId\":21639,\"journal\":{\"name\":\"SEPARATION SCIENCE PLUS\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-12-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"SEPARATION SCIENCE PLUS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/sscp.202300195\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"SEPARATION SCIENCE PLUS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/sscp.202300195","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

本研究建立了一种快速、经济的萃取预浓缩方法——气泡辅助分散液相微萃取法,用于分析不同葡萄汁中农药的含量。为了推进微萃取方法,将样品转移到锥形底玻璃试管中,加入氯化铵并旋转溶解。然后,加入碳酸氢钠和1,2 -二溴乙烷和正己烷的混合物。该管位于水浴中,产生的二氧化碳气泡将萃取溶剂分散到样品中。最后将沉淀相离心,取1微升注入装有火焰电离检测器的气相色谱仪中。在最佳条件下,检测限为0.9 ~ 4.1 μg/L,定量限为3.0 ~ 13.6 μg/L。提取回收率为36% ~ 80%,富集系数为180% ~ 404%。日间和日间的相对标准偏差分别在3.4%-10.6%和2.6%-9.7%之间。校正曲线的决定系数均≥0.990。提取时间短,不需要吸附剂或昂贵的仪器,使用廉价的化学品,使用微升级别的萃取剂,不稀释实际样品是该研究的亮点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Development of an effervescence‐assisted dispersive liquid phase microextraction using a binary solvent as a simultaneous extraction and preconcentration approach specialized for the analysis of pesticides in grape juice without dilution
In this study, a swift and economical extraction and preconcentration method called effervescence‐assisted dispersive liquid‐phase microextraction was developed to analyze the pesticide content of different grape juices. To propel the microextraction method, the sample was transferred to a conical bottom glass test tube, and ammonium chloride was added and vortexed to dissolve. Then, sodium bicarbonate and a mixture of 1,2‐dibromoethane and n‐hexane were added. The tube was located in a water bath and the produced carbon dioxide bubbles dispersed the extraction solvent into the sample. Finally, it was centrifuged and one microliter of the sedimented phase was injected into a gas chromatograph equipped with a flame ionization detector. Under the optimum conditions, the limits of detection and quantification ranged from 0.9 to 4.1 and 3.0 to 13.6 μg/L, respectively. Extraction recoveries and enrichment factors were achieved in the ranges of 36%–80% and 180%–404%, respectively. The inter‐ and intra‐day relative standard deviations were in the ranges of 3.4%–10.6% and 2.6%–9.7%, respectively. Also, the coefficients of determination in the calibration curves were ≥0.990. Short extraction time, no sorbent or costly apparatuses, using inexpensive chemicals, applying microliter levels of the extractant, and no dilution of the real samples are the highlights of the study.
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
SEPARATION SCIENCE PLUS
SEPARATION SCIENCE PLUS CHEMISTRY, ANALYTICAL-
CiteScore
1.90
自引率
9.10%
发文量
111
期刊最新文献
Removal of Residual DNA and Host Cell Proteins for the Purification of Recombinant Staphylokinase Expressed in Escherichia coli Green Analytical Approach for HPLC Method Development for Quantification of Sorafenib and Its Pharmacopeia Impurities: LC–MS/MS Characterization and Toxicity Prediction of Stress Degradation Products A Cartridge Structure Facilitates Clinical Mass Spectrometry Pretreatment and Can be Integrated Into a High‐Throughput Instrument Comparison of Polysaccharide Profiles of Different Seaweeds Based on Ion Chromatography and Ultrahigh‐Performance Liquid Chromatography Quantification of Recycled Polypropylene Stabilizers for Quality Control by Liquid Chromatography–Tandem Mass Spectrometry Using Simple, Fast and Efficient Ultrasonic Extraction
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1