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基于离子液体的单滴微萃取结合液相色谱-紫外分光光度检测法测定地表水中的典型紫外滤光剂。

Ionic liquid-based single-drop microextraction followed by liquid chromatography-ultraviolet spectrophotometry detection to determine typical UV filters in surface water samples.

机构信息

Departamento de Química Analítica, Nutrición y Bromatología e Instituto Universitario de Materiales, Universidad de Alicante, P.O. Box 99, E-03080, Alicante, Spain.

出版信息

Talanta. 2010 Apr 15;81(1-2):549-55. doi: 10.1016/j.talanta.2009.12.042. Epub 2010 Jan 4.

Abstract

A user-friendly and inexpensive ionic liquid-based single-drop microextraction (IL-SDME) procedure has been developed to preconcentrate trace amounts of six typical UV filters extensively used in cosmetic products (i.e., 2-hydroxy-4-methoxybenzophenone, isoamyl 4-methoxycinnamate, 3-(4'-methylbenzylidene)camphor, 2-ethylhexyl 2-cyano-3,3-diphenylacrylate, 2-ethylhexyl 4-dimethylaminobenzoate and 2-ethylhexyl 4-methoxycinnamate) from surface water samples prior to analysis by liquid chromatography-ultraviolet spectrophotometry detection (LC-UV). A two-stage multivariate optimization approach was developed by means of a Plackett-Burman design for screening and selecting the significant variables involved in the SDME procedure, which were later optimized by means of a circumscribed central composite design. The studied variables were drop volume, sample volume, agitation speed, ionic strength, extraction time and ethanol quantity. Owing to particularities, ionic liquid type and pH of the sample were optimized separately. Under optimized experimental conditions (i.e., 10 microL of 1-hexyl-3-methylimidazolium hexafluorophosphate, 20 mL of sample containing 1% (v/v) ethanol and NaCl free adjusted to pH 2, 37 min extraction time and 1300 rpm agitation speed) enrichment factors up to ca. 100-fold were obtained depending on the target analyte. The method gave good levels of repeatability with relative standard deviations varying between 2.8 and 8.8% (n=6). Limits of detection were found in the low microg L(-1) range, varying between 0.06 and 3.0 microg L(-1) depending on the target analyte. Recovery studies from different types of surface water samples collected during the winter period, which were analysed and confirmed free of all target analytes, ranged between 92 and 115%, showing that the matrix had a negligible effect upon extraction. Finally, the proposed method was applied to the analysis of different water samples (taken from two beaches, two swimming pools and a river) collected during the summer period.

摘要

一种用户友好且廉价的基于离子液体的单滴微萃取(IL-SDME)程序已经被开发出来,用于预浓缩痕量的六种常用于化妆品的典型紫外线滤光剂(即 2-羟基-4-甲氧基二苯甲酮、异戊基 4-甲氧基肉桂酸酯、3-(4'-甲基亚苄基)樟脑、2-乙基己基 2-氰基-3,3-二苯基丙烯酸酯、2-乙基己基 4-二甲基氨基苯甲酸酯和 2-乙基己基 4-甲氧基肉桂酸酯),然后通过液相色谱-紫外分光光度法(LC-UV)进行分析。通过 Plackett-Burman 设计开发了一种两阶段多元优化方法,用于筛选和选择 SDME 程序中涉及的重要变量,然后通过限定的中心复合设计对这些变量进行优化。研究的变量包括液滴体积、样品体积、搅拌速度、离子强度、萃取时间和乙醇量。由于特殊性,离子液体类型和样品的 pH 值分别进行了优化。在优化的实验条件下(即 10μL 1-己基-3-甲基咪唑六氟磷酸盐、20mL 含 1%(v/v)乙醇和无 NaCl 的样品,pH 值调至 2,萃取时间 37min,搅拌速度 1300rpm),根据目标分析物的不同,可获得高达约 100 倍的富集因子。该方法具有良好的重复性水平,相对标准偏差在 2.8%至 8.8%(n=6)之间变化。检出限在低μg L(-1)范围内,根据目标分析物的不同,在 0.06 至 3.0μg L(-1)之间变化。从冬季采集的不同类型地表水样品中进行的回收研究,这些样品经分析并确认不含所有目标分析物,回收率在 92%至 115%之间,表明基质对萃取的影响可以忽略不计。最后,该方法应用于不同水样(取自两个海滩、两个游泳池和一条河流)的分析,这些水样均取自夏季。

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