Keywords
‘click’ reaction
closo-decaborate
in vivo study
azido derivative
BODIPY
boron neutron capture therapy
fluorescent labeling
Abstract
A water-soluble conjugate of closo-decaborate derivative with BODIPY was synthesized using the copper-catalyzed azide–alkyne cycloaddition. The absorption and emission spectra of the formed conjugate show that the addition of a boron cluster weakens the fluorescence of the initial azido derivative of BODIPY. The biodistribution of this conjugate in the in in vivo study on laboratory animals reveales a high tumor-to-normal-tissue ratio, making it a potential candidate for boron neutron capture therapy.
Funders
Russian Science Foundation
24-73-10090
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