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Biodistribution of Multimodal Gold Nanoclusters Designed for Photoluminescence-SPECT/CT Imaging and Diagnostic

Highly biocompatible nanostructures for multimodality imaging are critical for clinical diagnostics improvements in the future. Combining optical imaging with other techniques may lead to important advances in diagnostics. The purpose of such a system would be to combine the individual advantages of...

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Detalles Bibliográficos
Autores principales: Jarockyte, Greta, Stasys, Marius, Poderys, Vilius, Buivydaite, Kornelija, Pleckaitis, Marijus, Bulotiene, Danute, Matulionyte, Marija, Karabanovas, Vitalijus, Rotomskis, Ricardas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9565908/
https://www.ncbi.nlm.nih.gov/pubmed/36234387
http://dx.doi.org/10.3390/nano12193259
Descripción
Sumario:Highly biocompatible nanostructures for multimodality imaging are critical for clinical diagnostics improvements in the future. Combining optical imaging with other techniques may lead to important advances in diagnostics. The purpose of such a system would be to combine the individual advantages of each imaging method to provide reliable and accurate information at the site of the disease bypassing the limitations of each. The aim of the presented study was to evaluate biodistribution of the biocompatible technetium-99m labelled bovine serum albumin–gold nanoclusters ((99m)Tc-BSA-Au NCs) as photoluminescence-SPECT/CT agent in experimental animals. It was verified spectroscopically that radiolabelling with (99m)Tc does not influence the optical properties of BSA-Au NCs within the synthesized (99m)Tc-BSA-Au NCs bioconjugates. Biodistribution imaging of the (99m)Tc-BSA-Au NCs in Wistar rats was performed using a clinical SPECT/CT system. In vivo imaging of Wistar rats demonstrated intense cardiac blood pool activity, as well as rapid blood clearance and accumulation in the kidneys, liver, and urinary bladder. Confocal images of kidney, liver and spleen tissues revealed no visible uptake indicating that the circulation lifetime of (99m)Tc-BSA-Au NCs in the bloodstream might be too short for accumulation in these tissues. The cellular uptake of (99m)Tc-BSA-Au NCs in kidney cells was also delayed and substantial accumulation was observed only after 24-h incubation. Based on our experiments, it was concluded that (99m)Tc-BSA-Au NCs could be used as a contrast agent and shows promise as potential diagnostic agents for bloodstream imaging of the excretory organs in vivo.