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固相萃取-高效液相色谱-蒸发光散射检测法同时检测食品中5种人工合成甜味剂
引用本文:Liu F,Wang Y,Wang Y,Zhou J,Yan C. 固相萃取-高效液相色谱-蒸发光散射检测法同时检测食品中5种人工合成甜味剂[J]. 色谱, 2012, 30(3): 292-297. DOI: 10.3724/SP.J.1123.2011.11034
作者姓名:Liu F  Wang Y  Wang Y  Zhou J  Yan C
作者单位:1. 上海交通大学药学院, 上海 200240; 2. 上海通微分析技术有限公司, 上海 201203; 3. 华东师范大学化学系, 上海 200062
基金项目:国家自然科学基金项目(21175092,21105064);国家重大科学仪器设备开发专项(2011YQ150072,2011YQ15007204,2011YQ15007207,2011YQ15007210)
摘    要:建立了高效液相色谱-蒸发光散射检测仪(HPLC-ELSD)同时检测食品中安赛蜜、糖精钠、甜蜜素、三氯蔗糖和阿斯巴甜5种甜味剂的方法。甜味剂经0.1%(v/v)甲酸缓冲液提取后,利用C18固相萃取小柱净化浓缩,以3 μm C18柱为分离柱,0.1%(v/v)甲酸(氨水调节pH=3.5)-甲醇(61:39, v/v)为流动相,经高效液相色谱法分离,蒸发光散射检测器进行检测。结果表明,5种甜味剂在30~1000 mg/L的范围内,具有良好的线性关系(相关系数大于0.997);在3个添加水平下,样品的平均回收率为85.6%~109.0%,相对标准偏差小于4.0%;方法检出限(LOD,信噪比(S/N)=3)分别为安赛蜜2.5 mg/L、糖精钠3 mg/L、甜蜜素10 mg/L、三氯蔗糖2.5 mg/L及阿斯巴甜5 mg/L。该方法简单、灵敏、操作成本低,可用于不同形态食品中多种甜味剂的同时检测。

关 键 词:固相萃取  高效液相色谱  蒸发光散射检测  甜味剂  食品安全
收稿时间:2011-11-21

Simultaneous determination of five synthetic sweeteners in food by solid phase extraction-high performance liquid chromatography-evaporative light scattering detection
Liu Fang,Wang Yan,Wang Yuhong,Zhou Junyi,Yan Chao. Simultaneous determination of five synthetic sweeteners in food by solid phase extraction-high performance liquid chromatography-evaporative light scattering detection[J]. Chinese journal of chromatography, 2012, 30(3): 292-297. DOI: 10.3724/SP.J.1123.2011.11034
Authors:Liu Fang  Wang Yan  Wang Yuhong  Zhou Junyi  Yan Chao
Affiliation:School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.
Abstract:A high performance liquid chromatographic method with evaporative light scattering detection (HPLC-ELSD) was developed for the simultaneous determination of five synthetic sweeteners (acesulfame-K, saccharin sodium, sodium cyclamate, sucralose and aspartame) in food. The sweeteners were extracted by 0.1% (v/v) formic acid buffer solution. The extract of sample was cleaned up and concentrated with solid phase extraction (SPE) cartridge. Then the sweeteners were separated on a C18 column (3 microm) using 0.1% (v/v) formic acid buffer (adjusted to pH = 3.5 with aqueous ammonia solution)-methanol (61: 39, v/v) as mobile phase, and finally detected by ELSD. The results showed that the reasonable linearity was achieved for all the analytes over the range of 30 - 1000 mg/L with the correlation coefficients (r) greater than 0.997. The recoveries for the five sweeteners ranged from 85.6% to 109.0% at three spiked concentrations with the relative standard deviations (RSDs) lower than 4.0%. The limits of detection (LODs, S/N = 3) were 2.5 mg/L for both acesulfame-K and sucralose, 3 mg/L for saccharin sodium, 10 mg/L for sodium cyclamate, and 5 mg/L for aspartame. The method is simple, sensitive and low cost, and has been successfully applied to the simultaneous determination of the five synthetic sweeteners in food.
Keywords:solid-phase extraction(SPE)  high performance liquid chromatography(HPLC)  evaporative light scattering detection(ELSD)  sweeteners  food safety
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