Salehirozveh Mostafa, Bonné Robin, Kumar Peeyush, Abazar Farbod, Dehghani Parisa, Mijakovic Ivan, Roy Vellaisamy A L
Division of Systems and Synthetic Biology, Department of Life Sciences, Chalmers University of Technology, SE-41296, Gothenburg, Sweden.
Center for Electromicrobiology (CEM), Aarhus University, Ny Munkegade 114, 8000 Aarhus, Denmark.
Nanoscale. 2025 Feb 20;17(8):4543-4555. doi: 10.1039/d4nr04228j.
Neurodegenerative diseases, characterized by the progressive deterioration of neuronal function and structure, pose significant global public health and economic challenges. Brain-Derived Neurotrophic Factor (BDNF), a key regulator of neuroplasticity and neuronal survival, has emerged as a critical biomarker for various neurodegenerative and psychiatric disorders, including Alzheimer's disease. Traditional diagnostic methods, such as Enzyme-Linked Immunosorbent Assay (ELISA) and electrochemiluminescence (ECL) assays, face limitations in terms of sensitivity, stability, reproducibility, and cost-effectiveness. In this research, we developed the first electrical aptasensor for BDNF detection, constructed on a flexible polyimide (PI) membrane coated with reduced graphene oxide (r-GO) and utilized an extended-gate field-effect transistor (EGFET) as the transducer. Comprehensive characterization of the sensor, coupled with the fine-tuning of aptamer concentration and the binding time of DNA aptamers to the chemical linker, was achieved through Electrochemical Impedance Spectroscopy (EIS) to boost sensitivity. Consequently, by utilizing the unique properties of r-GO and DNA aptamers, the aptasensor exhibited exceptional detection abilities, with a detection limit as low as 0.4 nM and an extensive response range spanning from 0.025 to 1000 nM. The flexible PI-based electrode offers exceptional stability, affordability, and durability for home diagnostics, enriched by the reusability of its electronic transducer, making the device highly portable and suitable for prolonged monitoring. Our aptasensor surpasses traditional methods, showcasing superior real-time performance and reliability. The high sensitivity and specificity of our aptasensor highlight its potential to significantly improve early diagnosis and therapeutic monitoring of neurodegenerative diseases such as Alzheimer's, representing a considerable advancement in the diagnosis and management of such conditions.
神经退行性疾病以神经元功能和结构的进行性恶化为特征,给全球公共卫生和经济带来了重大挑战。脑源性神经营养因子(BDNF)作为神经可塑性和神经元存活的关键调节因子,已成为包括阿尔茨海默病在内的各种神经退行性和精神疾病的重要生物标志物。传统诊断方法,如酶联免疫吸附测定(ELISA)和电化学发光(ECL)测定,在灵敏度、稳定性、重现性和成本效益方面存在局限性。在本研究中,我们开发了首个用于检测BDNF的电化学适体传感器,该传感器构建在涂有还原氧化石墨烯(r-GO)的柔性聚酰亚胺(PI)膜上,并采用扩展栅场效应晶体管(EGFET)作为换能器。通过电化学阻抗谱(EIS)对传感器进行全面表征,并对适体浓度和DNA适体与化学连接体的结合时间进行微调,以提高灵敏度。因此,利用r-GO和DNA适体的独特性质,该适体传感器表现出卓越的检测能力,检测限低至0.4 nM,响应范围广泛,从0.025 nM到1000 nM。基于柔性PI的电极具有出色的稳定性、经济性和耐用性,适用于家庭诊断,其电子换能器的可重复使用性进一步增强了这些特性,使该设备具有高度便携性,适合长期监测。我们的适体传感器超越了传统方法,展现出卓越的实时性能和可靠性。我们适体传感器的高灵敏度和特异性突出了其在显著改善阿尔茨海默病等神经退行性疾病的早期诊断和治疗监测方面的潜力,代表了此类疾病诊断和管理方面的重大进展。