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Molecularly imprinted surface plasmon resonance (SPR) based sensing of bisphenol A for its selective detection in aqueous systems

机译:基于分子印迹表面等离振子共振(SPR)的双酚A感测在水性系统中的选择性检测

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Bisphenol A (BPA) imprinted poly(ethylene glycol dimethacrylate-N-methacryloyl-L-phenylalanine-vinyl imidazole) [poly(EGDMA-MAPA-VI)] film deposition on a SPR sensor with improved efficiency is described in this paper. The molecularly imprinted SPR sensor was characterized by FTIR-ATR, atomic force microscopy and ellipsometry. A water-compatible molecularly imprinted film has been developed for rapid, sensitive, and label-free detection of BPA in aqueous solutions prepared in Milli Q water, tap water and synthetic wastewater. The real-time response allows the detection of BPA with concentrations ranging from 0.08 to 10 ??g La?’1 with LOD and LOQ values of 0.02 and 0.08 ??g La?’1 in Milli Q water, 0.06 and 0.2 ??g La?’1 in tap water and 0.08 and 0.3 ??g La?’1 in synthetic wastewater, respectively. A significant increase in sensitivity was therefore expected due to the use of the imprinted poly(EGDMA-MAPA-VI) thin film. The method showed good recoveries and precision for the samples spiked with BPA. The results suggest that the imprinted SPR sensing method can be used as a promising alternative for the detection of BPA. The sensor data fitted well with the Langmuir adsorption model. The selectivity studies showed that the imprinted cavities formed in the polymeric nanofilm recognize BPA preferentially rather than 4-nitrophenol, hydroquinone, phenol and 8-hydroxy quinoline with a relative selectivity coefficient of 2.5, 2.6, 2.7 and 2.5, respectively. The prepared BPA imprinted SPR sensor enables high sensitivity, label-free detection, real-time monitoring, low volume sample consumption, quantitative evaluation, and determination of kinetic rate constants very well. In addition, the SPR based BPA sensor is easy to use and can be a cost effective solution due to the reusability of the prepared sensor. Furthermore, the storage stability will be higher than antibody-based detection methods.
机译:本文描述了在SPR传感器上以更高的效率沉积双酚A(BPA)印迹的聚(乙二醇二甲基丙烯酸酯-N-甲基丙烯酰基-L-苯丙氨酸-乙烯基咪唑)[聚(EGDMA-MAPA-VI)]膜。分子印迹SPR传感器通过FTIR-ATR,原子力显微镜和椭圆光度法进行了表征。已开发出一种与水相容的分子印迹膜,用于在Milli Q水,自来水和合成废水中制备的水溶液中快速,灵敏且无标签地检测BPA。实时响应允许在Milli Q水,0.06和0.2Ω的水中检测到BPA的浓度范围为0.08到10ΔgLa -1',LOD和LOQ值为0.02和0.08ΔgLa -1'。自来水中的g La?'1和合成废水中的g?La?'1分别为0.08和0.3?g La?'1。因此,由于使用了压印的聚(EGDMA-MAPA-VI)薄膜,因此灵敏度有望显着提高。该方法对加有BPA的样品具有良好的回收率和精密度。结果表明,印迹SPR传感方法可以用作检测BPA的有前途的替代方法。传感器数据与Langmuir吸附模型非常吻合。选择性研究表明,在聚合物纳米膜中形成的印迹腔优先识别BPA,而不是4-硝基苯酚,氢醌,苯酚和8-羟基喹啉,相对选择性系数分别为2.5、2.6、2.7和2.5。制备的BPA印迹SPR传感器可实现高灵敏度,无标签检测,实时监控,少量样品消耗,定量评估以及动力学速率常数的测定。此外,基于SPR的BPA传感器易于使用,并且由于准备好的传感器的可重复使用性,因此可以是一种经济高效的解决方案。此外,储存稳定性将高于基于抗体的检测方法。

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