Nano-bio-photonics Lab, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran.
Nano-bio-photonics Lab, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran.
Talanta. 2024 Nov 1;279:126593. doi: 10.1016/j.talanta.2024.126593. Epub 2024 Jul 20.
A surface plasmon resonance imaging (SPRI)-based biosensor is demonstrated for the detection of both hydrogen peroxide (HO) and glucose. The HO to be detected acts as an oxidant and etch the silver film. This process gradually effects on resonance condition and consequently the reflected light intensity at a fixed angle. The etching rate of the silver film shows a clear relation with the HO concentration. Therefore, monitoring the reflected light intensity progressively changing over a few minutes, enables accurate detection of HO concentrations ranging from 0 to 200 μM (within physiological range of 0.25-50 μM), with a remarkable limit of detection (LOD) as low as 40 nM. In this regard, the behavior of the surface plasmon resonance (SPR) dip in response to the reduction of the silver film thickness is predicted by Winspall simulation software. These simulation results are in good agreement with the experimental results. Moreover, the proposed method can be applied to determine glucose concentrations ranging from 0 to 10 mM, encompassing the physiological range of 3-8 mM. This is achieved by observing the generated HO through the enzymatic oxidation reaction between glucose and glucose oxidase (Gox). The sensor demonstrates remarkable sensitivity and selectivity, with a detection limit as low as 175 μM for glucose concentration. Furthermore, accurate measurement of glucose concentration in an actual human serum sample is achievable with the proposed sensor, using the standard addition method. The suggested glucose sensor shows promising prospects for use in routine glucose testing, employing a label-free, real-time, and multiplex detection approach.© 2017 Elsevier Inc. All rights reserved.
一种基于表面等离子体共振成像(SPRI)的生物传感器被用于检测过氧化氢(HO)和葡萄糖。待检测的 HO 充当氧化剂并蚀刻银膜。这个过程逐渐影响共振条件,从而影响在固定角度的反射光强度。银膜的蚀刻速率与 HO 浓度之间存在明显的关系。因此,通过监测几分钟内逐渐变化的反射光强度,可以准确检测出 0 到 200μM(生理范围内 0.25-50μM)范围内的 HO 浓度,其检测限(LOD)低至 40nM。在这方面,通过 Winspall 模拟软件预测了表面等离子体共振(SPR)的行为,以响应银膜厚度的减少。这些模拟结果与实验结果吻合良好。此外,该方法可用于检测 0 到 10mM 的葡萄糖浓度,涵盖生理范围内的 3-8mM。这是通过观察葡萄糖和葡萄糖氧化酶(Gox)之间的酶促氧化反应产生的 HO 来实现的。该传感器具有出色的灵敏度和选择性,对葡萄糖浓度的检测限低至 175μM。此外,通过使用标准添加法,可使用该传感器对实际人血清样本中的葡萄糖浓度进行准确测量。所提出的葡萄糖传感器具有在常规葡萄糖测试中应用的广阔前景,采用无标记、实时和多重检测方法。© 2017 爱思唯尔公司。保留所有权利。