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离子液体基基质固相分散结合均匀液-液微萃取用于调味品中合成色素的分析

Ionic liquid-based matrix solid-phase dispersion coupled with homogeneous liquid-liquid microextraction of synthetic dyes in condiments.

作者信息

Wang Zhibing, Zhang Liyuan, Li Na, Lei Lei, Shao Mingyuan, Yang Xiao, Song Ying, Yu Aimin, Zhang Hanqi, Qiu Fangping

机构信息

College of Chemistry and Life Science, Changchun University of Technology, Changchun 130012, China; College of Chemistry, Jilin University, Changchun 130012, China.

College of Chemistry, Jilin University, Changchun 130012, China; College of Food, Heilongjiang Bayi Agricultural University, Daqing 163319, China.

出版信息

J Chromatogr A. 2014 Jun 27;1348:52-62. doi: 10.1016/j.chroma.2014.04.086. Epub 2014 May 2.

Abstract

The ionic liquid-based matrix solid-phase dispersion homogeneous liquid-liquid microextraction (IL-based MSPD-HLLME) was developed and applied to the extraction of four banned dyes, including chrysoidin, safranine O, auramine O and rhodamine B, in condiment samples. High performance liquid chromatography was applied to the separation and determination of the analytes. The solid sample was directly treated by MSPD using ionic liquid as dispersant and the eluate obtained in MSPD was treated by HLLME. Some experimental parameters, including type of dispersant, ratio of sample to dispersant, type and volume of ionic liquid, type and volume of elution solvent, pH value and ionic strength of the elution solvent, amount of ion-pairing agent (NH4PF6) and extraction time, were investigated and optimized. The linearities for determining the analytes were in the range of 60-2000μgkg(-1) for chrysoidin, 40-2000μgkg(-1) for safranine O and 20-1000μgkg(-1) for auramine O and rhodamine B, with the correlation coefficients ranging from 0.9964 to 0.9991. The limits of detection for the analytes were between 6.7 and 26.8μgkg(-1) and the limits of quantification were between 15.99 and 58.48μgkg(-1). When the present method was applied to the analysis of spiked condiment samples, the recoveries of the analytes ranged from 90.69 to 113.52% and relative standard deviations were lower than 8.2%. The present method combined the advantages of MSPD and HLLME, and could be applied for the determination of synthetic dyes in condiment samples.

摘要

基于离子液体的基质固相分散均相液液微萃取(IL基MSPD-HLLME)被开发并应用于调味品样品中四种禁用染料(包括碱性菊橙、番红O、金胺O和罗丹明B)的萃取。采用高效液相色谱法对分析物进行分离和测定。固体样品用离子液体作为分散剂通过MSPD直接处理,MSPD中获得的洗脱液再通过HLLME处理。考察并优化了一些实验参数,包括分散剂类型、样品与分散剂的比例、离子液体的类型和体积、洗脱溶剂的类型和体积、洗脱溶剂的pH值和离子强度、离子对试剂(NH4PF6)的用量以及萃取时间。测定分析物的线性范围为:碱性菊橙60 - 2000μgkg(-1)、番红O 40 - 2000μgkg(-1)、金胺O和罗丹明B 20 - 1000μgkg(-1),相关系数范围为0.9964至0.9991。分析物的检测限在6.7至26.8μgkg(-1)之间,定量限在15.99至58.48μgkg(-1)之间。当该方法应用于加标调味品样品分析时,分析物的回收率在90.69%至113.52%之间,相对标准偏差低于8.2%。该方法结合了MSPD和HLLME的优点,可用于测定调味品样品中的合成染料。

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