High purity insoluble dietary fiber from okara (Okara-HPIDF) is a raw material with a potentially positive effect on colon health. However, the mechanisms of the effect are far from clear....
Accurate
quantification of amyloid beta (Aβ) plaques
is an
important indicator for Alzheimer’s disease diagnosis and treatment.
For this purpose, new highly sensitive Aβ tracers
were designed by regulating the position and number of nitrogen atoms.
A series of derivatives of florbetapir (AV45) containing different
numbers and positions of N atoms were synthesized
and evaluated for in vitro affinity and in vivo biodistribution. Preliminary
study results showed that [18F]BIBD-124 and [18F]BIBD-127 had better clearance rates and less in vivo defluorination
than AV45 in ICR (ICR = Institute of Cancer Research) mice. Autoradiography
and molecular docking indicated that the binding sites of [18F]BIBD-124/127 were similar to that of [18F]AV45. Micro-positron
emission tomography-computed tomography imaging further demonstrated
that [18F]BIBD-124 could monitor Aβ plaques similar
to [18F]AV45. Besides, the imaging contrast of [18F]BIBD-124 is better than that of [18F]AV45. Mass spectrometric
metabolic analysis showed that BIBD-124 was less demethylated than
AV45 without subsequent acetylation, which might explain its less
non-specific uptake and higher imaging contrast. Gauss calculations
further confirmed that the introduction of N5 in
[18F]BIBD-124 decreased demethylation. Considering imaging
contrast and in vivo defluorination, [18F]BIBD-124 is expected
to be a promising radiotracer of Aβ plaques for further clinical
trials.
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