TY - JOUR
T1 - Optical Fibers Functionalized with Single-Walled Carbon Nanotubes for Flexible Fluorescent Catecholamine Detection
AU - Klinger, Madeline E.
AU - Miller, Rigney A.
AU - Komatsu, Natsumi
AU - Shiu, Amanda
AU - Wilbrecht, Linda
AU - Landry, Markita P.
N1 - We thank J. Travis Del Bonis-O’Donnell, Ph.D., for feedback and direction regarding silanization and M. Moein Safaee, Ph.D., for assistance constructing the fiber photometry rig. We acknowledge support of a Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI) (M.P.L. and N.K.), a Dreyfus Foundation Award (MPL), the Philomathia Foundation (MPL), an NIH MIRA Award R35GM128922 (M.P.L.), an NIH R21 NIDA Award 1R03DA052810 (M.P.L.), an NIH R21 NIDA Award R21DA044010 (to L.W. and M.P.L.), an NSF CAREER Award 2046159 (M.P.L.), an NSF CBET Award 1733575 (to M.P.L.), a CZI Imaging Award (M.P.L.), a Sloan Foundation Award (M.P.L.), a McKnight Foundation Award (M.P.L.), a Simons Foundation Award (M.P.L.), a Moore Foundation Award (M.P.L.), a Schmidt Foundation Award (M.P.L.), and Schmidt Science Fellows (N.K.). M.P.L. is a Chan Zuckerberg Biohub Investigator and a Hellen Wills Neuroscience Institute Investigator.
We acknowledge support of a Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI) (M.P.L. and N.K.), a Dreyfus Foundation Award (MPL), the Philomathia Foundation (MPL), an NIH MIRA Award R35GM128922 (M.P.L.), an NIH R21 NIDA Award 1R03DA052810 (M.P.L.), an NIH R21 NIDA Award R21DA044010 (to L.W. and M.P.L.), an NSF CAREER Award 2046159 (M.P.L.), an NSF CBET Award 1733575 (to M.P.L.), a CZI Imaging Award (M.P.L.), a Sloan Foundation Award (M.P.L.), a McKnight Foundation Award (M.P.L.), a Simons Foundation Award (M.P.L.), a Moore Foundation Award (M.P.L.), a Schmidt Foundation Award (M.P.L.), and Schmidt Science Fellows (N.K.). M.P.L. is a Chan Zuckerberg Biohub Investigator and a Hellen Wills Neuroscience Institute Investigator.
PY - 2025/4/22
Y1 - 2025/4/22
N2 - Despite the popularity of drugs that act on catecholamine receptors, our knowledge of catecholamine dynamics in human health and disease remains incomplete. Recent advances in fluorescent sensors have enabled unprecedented access to catecholamine dynamics in preclinical animal models, but the requirements of these technologies to use in model organisms limit their translational value for clinical diagnostics. Here, we introduce proof of principle fluorescent catecholamine detection via optical fibers functionalized with single-walled carbon nanotube (SWNT)-based near-infrared catecholamine sensors (nIRCats), a catecholamine detection form factor that has potential for more convenient and less invasive clinical translation. We show that these near-infrared functionalized (nIRF) fibers respond to dopamine in a biologically relevant concentration range (10 nM through 1 μM), with minimal responsivity loss following 16 h exposure to human blood plasma. We further demonstrate the utility of these fibers in detecting dopamine from as little as 10 μL volumes of clinically relevant biofluids up to 24 weeks after fiber synthesis. We also introduce a compact, mobile dual-near-infrared fiber photometry rig and demonstrate its success detecting dopamine in acute brain slices with nIRF fibers. Together, this fiber-based dopamine detection tool and photometry rig expand the toolset for catecholamine detection.
AB - Despite the popularity of drugs that act on catecholamine receptors, our knowledge of catecholamine dynamics in human health and disease remains incomplete. Recent advances in fluorescent sensors have enabled unprecedented access to catecholamine dynamics in preclinical animal models, but the requirements of these technologies to use in model organisms limit their translational value for clinical diagnostics. Here, we introduce proof of principle fluorescent catecholamine detection via optical fibers functionalized with single-walled carbon nanotube (SWNT)-based near-infrared catecholamine sensors (nIRCats), a catecholamine detection form factor that has potential for more convenient and less invasive clinical translation. We show that these near-infrared functionalized (nIRF) fibers respond to dopamine in a biologically relevant concentration range (10 nM through 1 μM), with minimal responsivity loss following 16 h exposure to human blood plasma. We further demonstrate the utility of these fibers in detecting dopamine from as little as 10 μL volumes of clinically relevant biofluids up to 24 weeks after fiber synthesis. We also introduce a compact, mobile dual-near-infrared fiber photometry rig and demonstrate its success detecting dopamine in acute brain slices with nIRF fibers. Together, this fiber-based dopamine detection tool and photometry rig expand the toolset for catecholamine detection.
UR - https://www.scopus.com/pages/publications/105003485600
UR - https://www.scopus.com/pages/publications/105003485600#tab=citedBy
U2 - 10.1021/acs.langmuir.4c04910
DO - 10.1021/acs.langmuir.4c04910
M3 - Article
C2 - 40223211
AN - SCOPUS:105003485600
SN - 0743-7463
VL - 41
SP - 9654
EP - 9663
JO - Langmuir
JF - Langmuir
IS - 15
ER -