Manfredi Anita, Giannetto Marco, Mattarozzi Monica, Costantini Monica, Mucchino Claudio, Careri Maria
Dipartimento di Chimica, Università degli Studi di Parma, Parco Area delle Scienze 17/A, 43124, Parma, Italy.
Anal Bioanal Chem. 2016 Oct;408(26):7289-98. doi: 10.1007/s00216-016-9494-z. Epub 2016 Mar 29.
The first competitive disposable amperometric immunosensor based on gliadin-functionalized carbon/nanogold screen-printed electrodes was developed for rapid determination of celiotoxic prolamins. To date, no competitive spectrophotometric or electrochemical immunoassays have yet been successfully applied to gluten detection in processed food samples, which require the use of complex prolamin extraction solutions containing additives with denaturing, reducing and disaggregating functions. Thus, in this work, great effort was put into the optimization and performance evaluation of the immunosensor in terms of suitability as a screening tool for analysis of cereal-based food samples. For this purpose, aqueous ethanol or complex extraction mixtures, as the patented Cocktail Solution®, were proved effective in the extraction of gliadin. Good sensitivity was achieved after optimization of the immunocompetitive assay, giving limit of detection and limit of quantitation of 8 and 22 ng/ml of gliadin, respectively, for ethanol extracts. The immunosensor was proved to be suitable also for samples extracted with Cocktail Solution® after a proper dilution. Analysis of real samples of different flours proved the suitability of the immunosensing device as a powerful tool for safety assessment of raw materials used for the formulation of dietary products for celiac disease patients. This immunosensor combines good analytical performance using a very simplified set-up protocol with suitability for rapid screening analysis performed using inexpensive and portable instrumentation. Graphical abstract Depiction of the development and working principle of the competitive immunosensor.
首个基于麦醇溶蛋白功能化碳/纳米金丝网印刷电极的竞争性一次性安培免疫传感器被开发用于快速测定细胞毒性醇溶蛋白。迄今为止,尚无竞争性分光光度法或电化学免疫分析法成功应用于加工食品样品中的麸质检测,这需要使用含有具有变性、还原和解聚功能添加剂的复杂醇溶蛋白提取溶液。因此,在这项工作中,我们在很大程度上致力于免疫传感器的优化和性能评估,以确定其作为基于谷物的食品样品分析筛选工具的适用性。为此,水乙醇或复杂提取混合物,即专利的鸡尾酒溶液®,被证明对麦醇溶蛋白的提取有效。在优化免疫竞争测定后获得了良好的灵敏度,乙醇提取物中麦醇溶蛋白的检测限和定量限分别为8和22 ng/ml。经适当稀释后,该免疫传感器也被证明适用于用鸡尾酒溶液®提取的样品。对不同面粉实际样品的分析证明,该免疫传感装置是一种强大的工具,可用于对乳糜泻患者膳食产品配方中使用的原材料进行安全性评估。这种免疫传感器结合了良好的分析性能,使用非常简化的设置方案,并且适用于使用廉价且便携的仪器进行快速筛选分析。图形摘要 竞争性免疫传感器的开发和工作原理示意图。