Department of Nanoengineering, University of California San Diego, La Jolla, California 92093, United States.
Departamento de Química Analítica, Universidad Complutense, E-28040 Madrid, Spain.
ACS Sens. 2023 Oct 27;8(10):3892-3901. doi: 10.1021/acssensors.3c01445. Epub 2023 Sep 21.
While paper-based lateral-flow immunoassays (LFA) offer considerable promise for centralized diagnostic applications, the analytical capability of conventional LFA remains constrained due to the low sensitivity of its common optical detection strategy. To address these issues, we report a simple electrochemical LFA (eLFA) with nanocatalytic redox cycling for decentralized insulin detection. Simultaneous binding of insulin with detection antibodies and capture antibodies through the capillary flow at the LFA platform and signal amplification through the rapid nanocatalytic reduction of [Fe(CN)] (Fe) with Au nanoparticles (AuNP) and ammonia-borane (AB), coupled to electrochemical redox cycling reactions involving Fe, AuNP, and AB on the carbon working electrode, offer higher sensitivity than conventional colorimetric LFA and enzymatic redox cycling. The resulting integrated eLFA strip allows the detection of low insulin concentrations (LOD = 12 pM) and offers considerable promise for highly sensitive decentralized assays of different biological fluids (saliva and serum) without additional pretreatment or washing steps.
虽然基于纸张的侧向流动免疫分析(LFA)为集中式诊断应用提供了巨大的潜力,但由于其常见的光学检测策略灵敏度较低,传统 LFA 的分析能力仍然受到限制。为了解决这些问题,我们报告了一种简单的电化学 LFA(eLFA),具有纳米催化氧化还原循环,用于分散式胰岛素检测。通过 LFA 平台上的毛细流动同时结合胰岛素与检测抗体和捕获抗体,并通过 Au 纳米粒子(AuNP)和氨硼烷(AB)快速纳米催化还原[Fe(CN)](Fe)进行信号放大,与涉及 Fe、AuNP 和 AB 的电化学氧化还原循环反应耦合,提供比传统比色 LFA 和酶促氧化还原循环更高的灵敏度。所得集成的 eLFA 条带允许检测低浓度的胰岛素(LOD = 12 pM),并且有望在无需额外预处理或洗涤步骤的情况下,对不同生物流体(唾液和血清)进行高度灵敏的分散式检测。