US2019224342A1PendingUtilityA1
Imaging Neurotransmitters In Vivo Using Functionalized Carbon Nanotubes
Est. expiryOct 9, 2036(~10.2 yrs left)· nominal 20-yr term from priority
Inventors:Markita P. Del Carpio LandryLinda A. WilbrechtJackson Travis Del Bonis-O'DonnellAbraham G. Beyene
B82Y 5/00Y10S977/927G01N 33/9406B82Y 15/00A61K 49/0054Y10S977/92Y10S977/75B82Y 30/00
45
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Claims
Abstract
Imaging based detection of changes in extracellular neurotransmitter concentration in living tissue is achieved using novel nanotube-based sensors. The sensors are functionalized, neurocompatible single-walled carbon nanotubes (SWNT) comprising an adsorbed neurotransmitter analyte selective polynucleotide.
Claims
exact text as granted — not AI-modified1 . A functionalized, neurocompatible single-walled carbon nanotube (SWNT) comprising an adsorbed neurotransmitter analyte selective polynucleotide covalently bound to a neurocompatible polyethyleneglycol (PEG).
2 . The nanotube of claim 1 wherein the polynucleotide is ssDNA or ssRNA
3 . The nanotube of claim 1 wherein the polynucleotide has a periodic purine-pyrimidine pattern.
4 . The nanotube of claim 1 wherein the polynucleotide is ssDNA or ssRNA; and
the polynucleotide has a periodic purine-pyrimidine pattern.
5 . The nanotube of claim 1 wherein the polynucleotide is ssDNA or ssRNA; and
the polynucleotide is polyGT is (GT)n, wherein n is an integer 4-30.
6 . The nanotube of claim 1 wherein the polynucleotide is ssDNA or ssRNA; and
the polynucleotide is polyGT is (GT)n, wherein n is 6.
7 . The nanotube of claim 1 wherein the analyte is a neurotransmitter selected from a catecholamine (e.g. epinephrine (adrenaline), norepinephrine (noradrenaline), and dopamine), histamine, 5-hydroxytryptamine (serotonin), γ-aminobutyric acid (GABA), glutamine, glutamic acid or a neurotransmitter metabolite selected from L-3,4-dihydroxyphenylalanine (L-dopa), 3,4-Dihydroxyphenylacetic acid (DOPAC), homovannilic acid and tyramine
8 . The nanotube of claim 1 wherein the analyte is dopamine.
9 . The nanotube of claim 1 wherein the PEG is PEG MW 400-20000.
10 . The nanotube of claim 1 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
11 . The nanotube of claim 2 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
12 . The nanotube of claim 3 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
13 . The nanotube of claim 4 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
14 . The nanotube of claim 5 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
15 . The nanotube of claim 6 wherein the analyte is dopamine; and
the PEG is PEG MW 400-20000.
16 . A functionalized, neurocompatible single-walled carbon nanotube (SWNT) comprising an adsorbed dopamine-selective polynucleotide of sequence (GT) 6 .
17 . The nanotube of claim 16 wherein the polynucleotide is covalently bound to a neurocompatible polyethyleneglycol (PEG).
18 . The nanotube of claiml 6 wherein the PEG is PEG MW 400-20000.
19 . The nanotube of claim 16 wherein the polynucleotide is covalently bound to a neurocompatible polyethyleneglycol (PEG); and
the PEG is PEG MW 400-20000.
20 . A method of imaging comprising: detecting changes in extracellular neurotransmitter concentration with the nanotube of claim 1 wherein the changes in extracellular neurotransmitter concentration are detected in neural tissue, and the nanotube is delivered to and/or located in live brain tissue in a brain slice or live mammal.Join the waitlist — get patent alerts
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