REQUIMTE, Serviço de Química-Física, Faculdade de Farmácia, Universidade do Porto, Rua Aníbal Cunha, 164, 4099-030 Porto, Portugal.
J Chromatogr A. 2010 May 28;1217(22):3575-82. doi: 10.1016/j.chroma.2010.03.035. Epub 2010 Mar 27.
For the first time, an automatic sample pre-treatment/detection method is proposed for the multiclass determination of UV filters (namely, benzophenone-3, ethylhexylmetoxycinnamate, butylmethoxydibenzoylmethane and homosalate) in environmental samples. The new methodology comprises in-line solid-phase extraction (SPE) of the target analytes by exploiting the bead injection (BI) concept in a mesofluidic lab-on-valve (LOV) format, with subsequent determination by liquid chromatography (LC). The proposed microanalytical system, using a multisyringe burette as propulsion unit, automatically performed the overall SPE steps, including the renewal of the sorbent in each analytical cycle to prevent sample cross-contamination and the post-extraction adjustment of the eluate composition to prevent chromatographic band broadening effects. In order to expedite the LC separation, a C(18) monolithic column was applied and an accelerated isocratic elution was carried out by using a cationic surfactant as mobile phase additive. The LOV-BI-LC method was proven reliable for handling and analysis of complex matrices, e.g., spiked swimming pool water and seawater, with limits of detection ranging between 0.45 and 3.2 microg L(-1) for 9 mL sample volume. Linear calibration was attained up to 160 microg L(-1) for homosalate and up to 35 microg L(-1) for the other target analytes, with good reproducibility (RSD<13%, for 5 different SPE columns). The hyphenated scheme is able to process a given sample simultaneously and within the same time frame than the chromatographic separation/determination of the formerly pre-treated sample, providing concentration values every 9 min. Hence, the sample throughput was enhanced up to 33 times when compared with previously reported off-line SPE methods. A drastic reduction in reagent consumption and effluent production was also attained, contributing to the development of an environment-friendly analyzer.
首次提出了一种自动样品预处理/检测方法,用于环境样品中紫外线滤光剂(即二苯甲酮-3、乙基己基甲氧基肉桂酸酯、丁基甲氧基二苯甲酰基甲烷和胡莫柳酯)的多类测定。新方法包括在介观流控阀(LOV)格式中利用珠注射(BI)概念对目标分析物进行在线固相萃取(SPE),随后通过液相色谱(LC)进行测定。所提出的微分析系统使用多注射器滴定管作为推进单元,自动执行整个 SPE 步骤,包括在每个分析循环中更新吸附剂以防止样品交叉污染和在洗脱后调整洗脱液组成以防止色谱带展宽效应。为了加快 LC 分离,应用了 C(18)整体柱,并通过使用阳离子表面活性剂作为流动相添加剂进行加速等度洗脱。LOV-BI-LC 方法被证明可靠,可用于处理和分析复杂基质,例如加标游泳池水和海水,对于 9 mL 样品体积,检测限范围在 0.45 到 3.2 µg L(-1)之间。对于胡莫柳酯,线性校准可达 160 µg L(-1),对于其他目标分析物,线性校准可达 35 µg L(-1),具有良好的重现性(5 根不同 SPE 柱的 RSD<13%)。该联用方案能够在与以前预处理样品的色谱分离/测定相同的时间内同时处理给定的样品,每 9 分钟提供一个浓度值。因此,与以前报道的离线 SPE 方法相比,样品通量提高了 33 倍。还大大减少了试剂消耗和废水产生,有助于开发环境友好型分析仪。