Investigation of electrocatalysis for tiered-tower micro-electro-mechanical-system-based biosensors: application in the early detection of the thrombosis factor trimethylamine N -oxide.

Autor: Lin WC; Department of Electrical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan. weiclin@mail.cgu.edu.tw.; Department of Trauma and Emergency, Chang Gung Memorial Hospital, Linko, 33302, Taiwan., Chou SC; Department of Electrical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan. weiclin@mail.cgu.edu.tw., Yen WL; Department of Electrical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan. weiclin@mail.cgu.edu.tw., Hsieh YY; Department of Electrical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan. weiclin@mail.cgu.edu.tw., Hsieh CT; Department of Electrical Engineering, Chang Gung University, Taoyuan, 33302, Taiwan. weiclin@mail.cgu.edu.tw.
Jazyk: angličtina
Zdroj: Nanoscale [Nanoscale] 2024 Oct 31; Vol. 16 (42), pp. 19897-19910. Date of Electronic Publication: 2024 Oct 31.
DOI: 10.1039/d4nr02693d
Abstrakt: Trimethylamine N -oxide (TMAO) has been recognized as a biomarker for the early detection of thrombosis. However, testing for TMAO typically requires expensive laboratory equipment and skilled technicians, making it unsuitable for home care pre-screening. To enable its widespread use in home applications, it is crucial to develop a scalable and sensitive device capable of catalyzing TMAO metabolism with a specific enzyme that is tailored for point-of-care use. This study presents an investigation of a MEMS-based two-tiered-tower biosensor array with a detection limit of 0.1 μM for TMAO, aiming to diagnose chronic metabolic diseases using urine or serum samples. Based on the augmented Cole-Cole model, the proposed parameters R _catalyzed , C _catalyzed , and R p_catalyzed can predict the catalytic impedance of enzymatic activities such as the redox effects of analytes and characterize the small-signal current caused by catalysis. The proposed MEMS biosensor, integrated with a readout circuitry, demonstrates a high sensitivity of 41 ADC counts per μM TMAO (or 4.5 mV μM -1 TMAO), a response time of 1 second, a repetition rate of 98.9%, and a drift over time of 0.5 mV. The sensor effectively distinguishes TMAO based on minute capacitance changes induced by the TorA enzyme, resulting in a discernible distinction of 10.6%. These measurements were successfully compared to conventional cyclic voltammetry (CV) results, showing a variance of only 0.024%. The proposed biosensor is well-suited for pre-screening thrombosis factors for the early detection and prevention of thrombosis in point-of-care applications. The device is cost-effective, lightweight, and demonstrates excellent performance, with a conversion rate of 88% of TMAO and a selectivity rate of 97% for the by-product TMA, allowing for the prediction of cardiovascular risks.
Databáze: MEDLINE