Department of Chemistry, Capital Normal University, Beijing, 100048, China.
Department of Chemistry, Capital Normal University, Beijing, 100048, China.
Talanta. 2024 Nov 1;279:126570. doi: 10.1016/j.talanta.2024.126570. Epub 2024 Jul 14.
The amplification strategies used for self-powered biosensor based on biofuel cell (BFC-SPB) need to be further developed. Because the currently developed strategies utilized the complicated hybridization of DNA or poorly readable current signal of capacitors for amplification, which limits the practical application in public health emergencies. Here, we present a facile chemical amplification strategy for BFC-SPB. The 5-min amplification was triggered by simply adding HO solution dropwise to the sensing cathode after the formation of the immune sandwich. The Ag NP of immunoprobe were oxidized to Ag(I), which can be served as the electron acceptor of the cathode. The amount of immunoprobe was positively correlated with that of the antigen, resulting in corresponding and high concentration of Ag(I) after the amplification, which enhanced the ability of the cathode as the electron acceptor. Meanwhile the glucose oxidation reaction (GOR) was performed on the bioanode modified with glucose oxidase (GOx). After assembling the bioanode and sensing cathode, the open circuit voltage of the BFC-SPB, measured by digital multimeter, distinctly rised with the elevated concentration of the antigen. To demonstrate the proof of concept, immunoglobulin G (IgG), selecting as a model analyte, was sensitively detected using this method. Result indicated that the limit of detection was 4.4 fg mL (0.03 amol mL) in the linear range of 1 pg mL-10 μg mL. This work initiates a brand-new way of chemical amplification strategy for BFC-SPB, and offers a promising platform for practical applications.
基于生物燃料电池(BFC-SPB)的自供电生物传感器的放大策略需要进一步发展。因为目前开发的策略利用了 DNA 的复杂杂交或电容器的可读性差的电流信号进行放大,这限制了其在公共卫生突发事件中的实际应用。在这里,我们提出了一种用于 BFC-SPB 的简便化学放大策略。在免疫三明治形成后,只需将 HO 溶液滴加到传感阴极上,即可触发 5 分钟的放大。免疫探针中的 Ag NP 被氧化为 Ag(I),可作为阴极的电子受体。免疫探针的数量与抗原的数量呈正相关,因此在放大后会产生相应的高浓度 Ag(I),从而增强了阴极作为电子受体的能力。同时,在修饰有葡萄糖氧化酶 (GOx) 的生物阳极上进行葡萄糖氧化反应 (GOR)。在组装生物阳极和传感阴极后,通过数字万用表测量 BFC-SPB 的开路电压,随着抗原浓度的升高,明显升高。为了证明概念验证,使用该方法灵敏地检测了免疫球蛋白 G (IgG)作为模型分析物。结果表明,在 1 pg mL-10 μg mL 的线性范围内,检测限为 4.4 fg mL(0.03 amol mL)。这项工作为 BFC-SPB 的化学放大策略开辟了一条全新的途径,并为实际应用提供了一个有前途的平台。