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Pivotal role of the protein corona in the cell uptake of fluorinated nanoparticles with increased sensitivity for (19)F-MR imaging

In vivo cell tracking by non-invasive imaging technologies is needed to accelerate the clinical translation of innovative cell-based therapies. In this regard, (19)F-MRI has recently gained increased attention for unbiased localization of labeled cells over time. To push forward the use of (19)F-MRI...

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Detalles Bibliográficos
Autores principales: Gatti, Lodovico, Chirizzi, Cristina, Rotta, Giulia, Milesi, Pietro, Sancho-Albero, María, Sebastián, Victor, Mondino, Anna, Santamaría, Jesús, Metrangolo, Pierangelo, Chaabane, Linda, Bombelli, Francesca Baldelli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334373/
https://www.ncbi.nlm.nih.gov/pubmed/37441254
http://dx.doi.org/10.1039/d3na00229b
Descripción
Sumario:In vivo cell tracking by non-invasive imaging technologies is needed to accelerate the clinical translation of innovative cell-based therapies. In this regard, (19)F-MRI has recently gained increased attention for unbiased localization of labeled cells over time. To push forward the use of (19)F-MRI for cell tracking, the development of highly performant (19)F-probes is required. PLGA-based NPs containing PERFECTA, a multibranched superfluorinated molecule with an optimal MRI profile thanks to its 36 magnetically equivalent fluorine atoms, are promising (19)F-MRI probes. In this work we demonstrate the importance of the surface functionalization of these NPs in relation to their interaction with the biological environment, stressing the pivotal role of the formation of the protein corona (PC) in their cellular labelling efficacy. In particular, our studies showed that the formation of PC NPs strongly promotes the cellular internalization of these NPs in microglia cells. We advocate that the formation of PC NPs in the culture medium can be a key element to be used for the optimization of cell labelling with a considerable increase of the detection sensitivity by (19)F-MRI.