501878 Carbon Nanotube Photoluminescence for in vivo Biosensors

Daniel Heller1, Jackson Harvey2, Prakrit Jena1, Thomas Galassi1, Ryan Williams1, Gül H. Zerze3, Jeetain Mittal4 and Daniel Roxbury5, (1)Memorial Sloan Kettering Cancer Center, New York, NY, (2)Memorial Sloan-Kettering Cancer Center, New York, NY, (3)Department of Chemical Engineering, Lehigh University, Bethlehem, PA, (4)Department of Chemical and Biomolecular Engineering, Lehigh University, Bethlehem, PA, (5)Chemical Engineering, University of Rhode Island, Richmond, RI

The real-time and spatially-resolved detection and identification of analytes in biological media present important goals for next-generation nanoscale probes and sensors. MicroRNAs and other small oligonucleotides in biofluids are promising disease biomarkers, yet conventional assays require complex processing steps that are unsuitable for point-of-care testing or for implantable or wearable sensors. To this end, we employ the intrinsic near-infrared fluorescence of single-walled carbon nanotubes which is photostable yet sensitive to the immediate environment. Here, we report an engineered carbon-nanotube-based sensor capable of real-time optical quantification of hybridization events of microRNA and other oligonucleotides. The mechanism of the sensor arises from competitive effects between displacement of both oligonucleotide charge groups and water from the nanotube surface, which result in a solvatochromism-like response. The sensor, which allows for detection via single-molecule sensor elements and for multiplexing by using multiple nanotube chiralities, can monitor toehold-based strand-displacement events, which reverse the sensor response and regenerate the sensor complex. We also show that the sensor functions in whole urine and serum, and can non-invasively measure DNA and microRNA after implantation in live mice.

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