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Development of an improved radioiodinated 2-phenylimidazo[1,2-a]pyridine for non-invasive imaging of amyloid plaquesElectronic supplementary information (ESI) available: Syntheses, 124I- labelling and all experimental procedures for biological evaluation. See DOI: 10.1039/c2md20115a
A series of novel phenyl-imidazo[1,2- a ]pyridines was evaluated in the context of developing improved imaging agents for β-amyloid (Aβ) in Alzheimer's disease (AD) and as a useful probe for in vitro studies. The results from binding experiments in vitro , together with biodistribution studies,...
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Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | A series of novel phenyl-imidazo[1,2-
a
]pyridines was evaluated in the context of developing improved imaging agents for β-amyloid (Aβ) in Alzheimer's disease (AD) and as a useful probe for
in vitro
studies. The results from binding experiments
in vitro
, together with biodistribution studies, autoradiography and
in vivo
stability studies demonstrated that radioiodinated 2-(4′-bromophenyl)-6-iodoimidazo[1,2-
a
]pyridine (
BrIMPY
,
4b
) is promising for preclinical and clinical imaging of Aβ. The no-carrier-added radioiodination of
4b
was successfully performed through an iododestannylation reaction from the corresponding trimethyltin derivative. [
125
I]
4b
and [
124
I]
4b
selectively labeled Aβ-plaques in brain tissue of an APP/PS1 mouse model of AD and their pattern of uptake showed excellent correlation with Aβ plaque pathology as measured by
ex vivo
immunohistochemistry. The present results suggest that radioiodinated
4b
possesses the properties needed as a tracer suitable for
in vivo
and
in vitro
studies, with potential for both PET and SPECT imaging of β-amyloid plaques in the living brain.
A series of novel phenyl-imidazo[1,2-
a
]pyridines was evaluated in the context of developing improved imaging agents for β-amyloid (Aβ) in Alzheimer's disease (AD) and as powerful
in vitro
probe. |
---|---|
ISSN: | 2040-2503 2040-2511 |
DOI: | 10.1039/c2md20115a |