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采用选择性吸附剂相的棒状吸附微萃取法测定实际基质中痕量水平的二苯甲酮型紫外线滤光剂。

Determination of trace levels of benzophenone-type ultra-violet filters in real matrices by bar adsorptive micro-extraction using selective sorbent phases.

机构信息

University of Lisbon, Faculty of Sciences, Chemistry and Biochemistry Department and Centre of Chemistry and Biochemistry, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.

出版信息

J Chromatogr A. 2013 Oct 11;1311:1-10. doi: 10.1016/j.chroma.2013.08.007. Epub 2013 Aug 7.

Abstract

Bar adsorptive micro-extraction (BAμE), using selective sorbent phases, followed by liquid desorption in combination with high performance liquid chromatography-diode array detection (BAμE-LD/HPLC-DAD), is proposed for the determination of trace levels of four benzophenone-type UV filters (benzophenone, 2-hydroxy-4-methoxy-benzophenone, 2,4-hydroxybenzophenone and 4-hydroxybenzophenone) in real matrices. By comparing three polymers (P1, P2 and P3) and five activated carbons (AC1, AC2, AC3, AC4 and AC5) phases, P2 (a modified pyrrolidone polymer) and AC4 coatings showed much higher selectivity and capacity through BAμE, where the former offers multiple mechanisms of interaction and faster equilibrium kinetics. Assays performed on 25mL of ultra-pure water samples spiked at the 8.0μg/L level, yielded recoveries ranging from 76.6±8.3% to 103.5±6.4% depending on the sorbent phase used (P2 or AC4), under optimized experimental conditions. The analytical performance showed convenient detection limits (0.3-0.5μg/L) and good linear dynamic ranges (1.0-24.0μg/L) with remarkable determination coefficients (r(2)>0.9969). Excellent repeatability was also achieved through intraday (RSD<13.0%) and interday (RSD<8.9%) experiments. By using the standard addition methodology, the application of the present analytical approach on sea water, wastewater, commercial cosmetic products and urine samples revealed good sensitivity, absence of matrix effects and the occurrence of levels of some benzophenones. The proposed methodology that uses nanostructured particles and operates under the floating sampling technology proved to be a sorption-based static micro-extraction alternative to monitor benzophenone-type UV filters in real matrices. Moreover, is easy to implement, reliable, sensitive, requiring low sample volume and the possibility to choose the most selective sorbent coating according to the target compounds involved.

摘要

采用选择性吸附剂的棒状吸附微萃取(BAμE),结合液相色谱-二极管阵列检测(BAμE-LD/HPLC-DAD)进行液体解吸,用于测定实际基质中痕量水平的四种二苯甲酮型紫外线滤光剂(二苯甲酮、2-羟基-4-甲氧基二苯甲酮、2,4-二羟基二苯甲酮和 4-羟基二苯甲酮)。通过比较三种聚合物(P1、P2 和 P3)和五种活性炭(AC1、AC2、AC3、AC4 和 AC5)相,P2(一种改性吡咯烷酮聚合物)和 AC4 涂层通过 BAμE 显示出更高的选择性和容量,前者提供了多种相互作用机制和更快的平衡动力学。在优化实验条件下,在 25mL 超纯水样品中加入 8.0μg/L 水平的物质进行测定,根据所用的吸附剂相(P2 或 AC4),回收率范围为 76.6±8.3%至 103.5±6.4%。分析性能显示出方便的检测限(0.3-0.5μg/L)和良好的线性动态范围(1.0-24.0μg/L),显著的决定系数(r²>0.9969)。通过日内(RSD<13.0%)和日间(RSD<8.9%)实验也获得了出色的重复性。通过标准添加方法,将本分析方法应用于海水、废水、商业化妆品产品和尿液样品中,显示出良好的灵敏度、不存在基质效应以及存在一些二苯甲酮的水平。该方法使用纳米结构颗粒并在浮采样技术下运行,被证明是一种基于吸附的静态微萃取替代方法,可用于监测实际基质中二苯甲酮型紫外线滤光剂。此外,该方法易于实施、可靠、灵敏,所需样品体积小,并可以根据目标化合物选择最具选择性的吸附剂涂层。

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