| Literature DB >> 33517230 |
Sultan Khetani1, Anupriya Singh1, Brendon Besler2, Savitri Butterworth2, Thomas Lijnse3, Kenneth Loughery2, Katrin Smith2, Ehsan Hosseini4, Rakesh Narang1, Kunal Karan4, Chantel Debert5, Arindom Sen6, Kartikeya Murari7, Amir Sanati- Nezhad8.
Abstract
Over 27 million individuals are affected every year worldwide with central nervous system (CNS) injuries. These injuries include but are not limited to traumatic brain injury (TBI) and spinal cord injury (SCI). CNS injuries remain a significant public health concern which demands reliable tools for rapid, on-sight, on-field, and point-of-care diagnostic (POC) solutions. To address these challenges, we developed a low-cost, open-source, hand-held, portable, and POC detection technology, termed as MicroDrop (μDrop), which can simultaneously detect up to eight target biomolecules and display results in both analog and digital formats. The data acquired is stored wirelessly in a cloud server for further investigation and statistical analysis. Multiplexing capability of μDrop and immuno-biosensors detects and quantifies Cleaved-Tau Protein (C-Tau) and Neuron-Filament (NFL) proteins in the blood of TBI patients. Immuno-biosensors rapidly sense the two target proteins in less than 30 min, with μDrop and a conventional potentiostat. C-Tau and NFL were selectively detected with μDrop within the dynamic range of 10 pg/mL - 100 ng/mL and the sensitivity range of 47 μA/pg mm2 - 65 μA/pg mm2. Comparing the biosensing performance with enzyme-linked immunosorbent assays (ELISA) shows that the immuno-biosensors combined with μDrop could successfully differentiate between clinical controls and injured patients.Entities:
Keywords: Biomedical device; Cleaved-tau protein (C-Tau); Electrochemical immuno-biosensor; Neuron filament protein (NFL); Traumatic brain injury (TBI)
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Year: 2021 PMID: 33517230 DOI: 10.1016/j.bios.2021.113033
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618