Surface Chemistry and Nanofabrication Unit, IK4-Tekniker, Eibar, Spain.
Surface Chemistry and Nanofabrication Unit, IK4-Tekniker, Eibar, Spain.
Anal Chim Acta. 2019 Nov 4;1079:94-102. doi: 10.1016/j.aca.2019.06.030. Epub 2019 Jun 13.
A shrimp tropomyosin (TPM) immunosensor has been developed and optimized to detect trace amounts of shrimp (in the ppm range), based on a combination of an amperometric transduction, magnetic particles and disposable screen-printed electrodes. The approach is based on the implementation of a sandwich immunoassay format on the surface of magnetic beads and their coupling onto disposable screen-printed electrodes to finally register the amperometric response at -200 mV vs. Ag pseudo-reference electrode, using HO as enzymatic substrate and hydroquinone as redox mediator. The use of carboxyl-functionalized magnetic microbeads (MBs) and in-house made magnetic nanoparticles (MNPs) as solid supports have been evaluated and compared. Our experimental results confirm that the use of MBs, in addition to simplifying the test protocol, improves the resulting sensitivity, so they were selected for the implementation of the immunosensor. In the optimized experimental conditions, the developed immunosensor offered a LOD of 47 pg mL for amperometric determination of shrimp TPM standards and great selectivity against TPM from other sources, thus allowing differentiation between crustaceans (shrimp) and mollusks (squid). Applicability studies demonstrated successful determination both in crude and cooked samples using very simple protocols. Additionally, processed foods based on fish and mollusks that could potentially include crustaceans in their composition have been analyzed using the sensor and compared to the declared ingredients. The sensitivity and specificity showed by the sensor in the analysis of heterogeneous food samples without a previous purification or enrichment stage, also outperforms existing solutions in terms of time and cost effectiveness and permits its direct and smooth implementation in the food industry for routine allergen analyses.
已开发并优化了一种虾原肌球蛋白 (TPM) 免疫传感器,用于检测痕量虾(ppm 级),该传感器基于电流变传感器、磁性颗粒和一次性丝网印刷电极的组合。该方法基于在磁性珠表面上实施夹心免疫测定格式及其偶联到一次性丝网印刷电极,最终在 -200 mV 相对于 Ag 伪参比电极处记录安培响应,使用 HO 作为酶底物和对苯二酚作为氧化还原介体。已评估和比较了羧基功能化磁性微球 (MBs) 和内部制造的磁性纳米颗粒 (MNPs) 作为固相载体的使用。我们的实验结果证实,除了简化测试方案外,MBs 的使用还提高了灵敏度,因此选择它们来实施免疫传感器。在优化的实验条件下,开发的免疫传感器对虾 TPM 标准的电流测定提供了 47 pg mL 的检出限和对其他来源的 TPM 的出色选择性,从而允许区分甲壳类动物(虾)和软体动物(鱿鱼)。应用研究表明,使用非常简单的方案,在粗制和熟制样品中都可以成功进行测定。此外,使用传感器分析了基于鱼类和贝类的加工食品,这些食品可能在其成分中包含甲壳类动物,并将其与所声明的成分进行了比较。传感器在分析无先前纯化或富集阶段的异质食品样品时表现出的灵敏度和特异性也优于现有解决方案,在时间和成本效益方面具有优势,并允许其在食品工业中直接顺利地用于常规过敏原分析。