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采用固相萃取和液相色谱-串联质谱法测定河水和废水中的高强度甜味剂。

Determination of high-intensity sweeteners in river water and wastewater by solid-phase extraction and liquid chromatography-tandem mass spectrometry.

作者信息

Arbeláez Paula, Borrull Francesc, Pocurull Eva, Marcé Rosa Maria

机构信息

Department of Analytical Chemistry and Organic Chemistry, Universitat Rovira i Virgili, Marcel-lí Domingo s/n, Campus Sescelades, Tarragona 43007, Spain.

Department of Analytical Chemistry and Organic Chemistry, Universitat Rovira i Virgili, Marcel-lí Domingo s/n, Campus Sescelades, Tarragona 43007, Spain.

出版信息

J Chromatogr A. 2015 May 8;1393:106-14. doi: 10.1016/j.chroma.2015.03.035. Epub 2015 Mar 21.

Abstract

High-intensity sweeteners have been suggested as potential organic contaminants due to their widespread use in food, drugs and sanitary products. As a consequence, they are introduced into the environment by different pathways, affecting aquatic life. In this study, a method based on solid-phase extraction (SPE) and liquid chromatography-tandem mass spectrometry (LC-MS-MS) has been developed and validated for the determination of eight sweeteners (saccharin, cyclamate, aspartame, acesulfame, neohesperidin dihydrochalcone, sucralose, stevioside and glycyrrhizic acid) in river water and wastewater. To get the maximum recoveries in SPE, several commercial sorbents were tested and Oasis HLB gave the best results, with recoveries higher than 41% for all of the compounds in the different matrices. Method limits of detection were in the range of 0.001-0.04μg/L in river water and 0.01-0.5μg/L in influent and effluent wastewater. Method reproducibility between days (n=5) was below 15% for all compounds. The method was applied to the determination of sweeteners in various river waters and wastewaters in Catalonia. Cyclamate, aspartame, neohesperidin dihydrochalcone, acesulfame and sucralose were found in river water, with the two last compounds being present at the highest values (1.62μg/L for acesulfame and 3.57μg/L for sucralose). In influent and effluent wastewater, all of the compounds were found at concentration levels ranging from 0.05 to 155μg/L except for stevioside and neohesperidin dihydrochalcone, which were not detected.

摘要

由于高强度甜味剂在食品、药品和卫生用品中广泛使用,它们被认为是潜在的有机污染物。因此,它们通过不同途径进入环境,影响水生生物。在本研究中,已开发并验证了一种基于固相萃取(SPE)和液相色谱 - 串联质谱(LC-MS-MS)的方法,用于测定河水和废水中的八种甜味剂(糖精、甜蜜素、阿斯巴甜、安赛蜜、新橙皮苷二氢查耳酮、三氯蔗糖、甜菊糖苷和甘草酸)。为了在固相萃取中获得最大回收率,测试了几种商用吸附剂,Oasis HLB效果最佳,不同基质中所有化合物的回收率均高于41%。河水的方法检测限在0.001 - 0.04μg/L范围内,进水和出水废水的检测限在0.01 - 0.5μg/L范围内。所有化合物的日间方法重现性(n = 5)低于15%。该方法应用于加泰罗尼亚地区各种河水和废水中甜味剂的测定。河水中发现了甜蜜素、阿斯巴甜、新橙皮苷二氢查耳酮、安赛蜜和三氯蔗糖,后两种化合物含量最高(安赛蜜为1.62μg/L,三氯蔗糖为3.57μg/L)。在进水和出水废水中,除未检测到的甜菊糖苷和新橙皮苷二氢查耳酮外,所有化合物的浓度水平在0.05至155μg/L之间。

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