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Rapid Multianalyte Quantification of Brain Chemistry Using Si-Nanoribbon Bio-Field-Effect Transistor Sensors.
Jesus Maldonado1, Vahulabaranan Rajagopalan2, Yue Gu1
1Department of Neurosurgery, Yale School of Medicine, New Haven, Connecticut 06510, United States.
This study introduces a novel CMOS-based nanosensor for real-time detection of key neurochemicals like gamma-aminobutyric acid (GABA), lactate, and glutamate, improving neurological disorder diagnostics.
Area of Science:
- Neuroscience
- Biomedical Engineering
- Materials Science
Background:
- Continuous monitoring of neurochemicals like gamma-aminobutyric acid (GABA), lactate, and glutamate is crucial for understanding neurological disorders.
- Existing semiconductor field-effect transistor (FET)-based sensors have limitations in real-time detection and surface functionalization.
Purpose of the Study:
- To develop a complementary metal-oxide-semiconductor (CMOS)-based FET nanowire device for rapid, real-time, and simultaneous biosensing of GABA, lactate, and glutamate.
- To engineer the sensor surface for selective detection in buffered solutions and complex biological matrices.
Main Methods:
- Utilized a CMOS-based FET nanowire (nanoribbon) platform.
- Employed aptamer bioreceptors for lactate and glutamate, and monoclonal antibodies for GABA.
- Functionalized the sensor surface for selective, label-free detection.
Main Results:
- Achieved rapid quantification of neurochemicals within 10 minutes.
- Demonstrated highly selective, label-free detection using aptamers and antibodies.
- Reported limits of detection (LOD) as low as 80 fM for GABA, 58 fM for glutamate, and 182 fM for lactate.
Conclusions:
- The developed nanosensing platform enables continuous neurochemical monitoring.
- This technology shows significant potential for improving diagnostic accuracy and therapeutic efficacy in neurological care.
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