Abstract
In this work, manifestations of IR luminescence sensitization of Indocyanine Green during conjugation with colloidal Ag2S quantum dots with an average size of 2.2 and 3.7 nm, passivated with thioglycolic acid molecules (Ag2S/TGA QDs) are studied using absorption and luminescence techniques. The possibility of enhancing luminescence in the dye monomer band (820 nm) under excitation at 660 nm by a factor of 6 in the presence of Ag2S/TGA QDs (2.2 nm) due to a decrease in the polymethine dye chain movement via coordination interaction with QDs was demonstrated. The way to switch-over from the first therapeutic window of biological tissue transparency (NIR-I, 700–950 nm) to the second (NIR-II, 1000–1700 nm), based on sensitization of IR luminescence of Ag2S/TGA QDs with an average size of 3.7 nm in the region of 1040 nm due to of resonance non-radiative transfer of excitation energy from Ag2S/TGA (2.2 nm) QDs at 900 nm to Ag2S/TGA QDs (3.7 nm) via the J-aggregate of ICG dye, which acts as an exciton bridge.
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The studies were financially supported by a grant the President of the Russian Federation for state support of young Russian scientists–candidates of sciences (MK-586.2019.2).
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The 2nd International School-Conference for young researchers “Smart Nanosystems for Life,” St. Petersburg, Russia, December 10–13, 2019.
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Kondratenko, T.S., Smirnov, M.S., Ovchinnikov, O.V. et al. IR Luminescence of Polyfunctional Associates of Indocyanine Green and Ag2S Quantum Dots. Opt. Spectrosc. 128, 1278–1285 (2020). https://doi.org/10.1134/S0030400X20080172
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DOI: https://doi.org/10.1134/S0030400X20080172