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Development of [ 18 F]SNFT‐1, a novel tau PET tracer with little off‐target binding
Author(s) -
Ishiki Aiko,
Harada Ryuichi,
Lerdsirisuk Pradith,
Yiqing Du,
Michinori Ezura,
Yanai Kazuhiko,
Furumoto Shozo,
Kudo Yukitsuka,
Arai Hiroyuki,
Okamura Nobuyuki
Publication year - 2020
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1002/alz.042298
Subject(s) - chemistry , biodistribution , monoamine oxidase , in vitro , monoamine oxidase b , binding potential , monoamine oxidase a , toxicity , receptor , pharmacology , biochemistry , enzyme , medicine , organic chemistry
Background [ 18 F]THK‐5351, which was originally designed to detect tau aggregates, bound to monoamine oxidase B (MAO‐B) with high affinity. Lead optimization toward selective binding profiles to tau has resulted in the development of novel selective tau PET tracer named [ 18 F]SNFT‐1 (THK‐5562). Here we present the preclinical characteristics of this tracer. Method In vitro competitive binding assays against MAO‐A, MAO‐B, amyloid, and tau were performed. In vitro autoradiography of the human brain tissues of various neurodegenerative diseases was performed. Receptor panel screen was performed to confirm the binding selectivity of this compound. Biodistribution study was performed in mice. In addition, an acute toxicity with intravenous administration of a single dose of this compound in mice was also investigated. Result SNFT‐1 showed high affinity ( K d = 0.47 nM) and selectivity for tau aggregates over other misfolding proteins as well as MAO enzymes. In vitro autoradiography demonstrated the intense laminar binding of [ 18 F]SNFT‐1 to tau pathology in AD and less off‐target binding than currently available tau PET tracers. No remarkable binding inhibition on various receptors ion channels, and transporters was observed at 1 μM concentration. [ 18 F]SNFT‐1 showed good initial brain uptake and rapid washout without defluorination and troublesome radiolabeled metabolites in mice. In acute toxicity study, no drug‐related changes were noted after intravenous administration of this compound in mice. Conclusion [ 18 F]SNFT‐1 is highly selective tau PET tracer, which will enable accurate monitoring of abnormal tau pathology in AD brain.