Departamento Química Analítica, Universidad de Alcalá, Ctra. Madrid-Barcelona, Km. 33,600, E-28871, Alcalá de Henares (Madrid), Spain.
Analyst. 2009 Dec;134(12):2405-11. doi: 10.1039/b911839j. Epub 2009 Oct 6.
A novel analytical strategy that couples enzyme-linked immunosorbent assay (ELISA) and electrochemical microfluidic chips to determine the mycotoxin zearalenone (ZEA) in baby foods is presented. The analytical cycles for an ultra-fast analysis of the sample and its sequential fast and simplified calibration were performed in about 200 s plus to ELISA protocol. This route avoided the typical four-parameter logistic curve fit which is a highly time-consuming and laborious procedure. An extremely low concentration level of ZEA (less than 1 ppb) was detected with reliability. This level is 20 times lower than the strictest tolerable limit (20 ppb) for baby foods, making the microfluidic approach the newly anticipated analytical security tool for the future. The reliability of the proposal was demonstrated by accuracy evaluations using a certified reference material and by demonstrating its suitability during the control of the regulatory limits of ZEA in baby foods. In addition, the microfluidic approach allowed sensitivity and the incubation enzymatic reaction to be manipulated in situ.
提出了一种将酶联免疫吸附测定(ELISA)和电化学微流控芯片相结合的新型分析策略,用于测定婴儿食品中的真菌毒素玉米赤霉烯酮(ZEA)。通过该分析方法,在大约 200 s 内即可完成对样品的超快速分析及其顺序快速和简化的校准,无需执行典型的四参数逻辑曲线拟合,该方法耗时耗力。该方法能够可靠地检测到极低浓度的 ZEA(低于 1 ppb),比婴儿食品的最严格可容忍限量(20 ppb)低 20 倍,使微流控方法成为未来新的预期分析安全工具。该方法的可靠性通过使用认证参考物质进行准确性评估以及在婴儿食品中 ZEA 监管限量的控制过程中证明其适用性得到了验证。此外,微流控方法还允许在原位操纵灵敏度和孵育酶反应。