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Etchable plasmonic nanoparticle probes to image and quantify cellular internalization

There is considerable interest in using nanoparticles as labels or to deliver drugs and other bioactive compounds to cells in vitro and in vivo. Fluorescent imaging, commonly used to study internalization and subcellular localization of nanoparticles, does not allow unequivocal distinction between c...

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Detalles Bibliográficos
Autores principales: Braun, Gary B., Friman, Tomas, Pang, Hong-Bo, Pallaoro, Alessia, de Mendoza, Tatiana Hurtado, Willmore, Anne-Mari A., Kotamraju, Venkata Ramana, Mann, Aman P., She, Zhi-Gang, Sugahara, Kazuki N., Reich, Norbert O., Teesalu, Tambet, Ruoslahti, Erkki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141013/
https://www.ncbi.nlm.nih.gov/pubmed/24907927
http://dx.doi.org/10.1038/nmat3982
Descripción
Sumario:There is considerable interest in using nanoparticles as labels or to deliver drugs and other bioactive compounds to cells in vitro and in vivo. Fluorescent imaging, commonly used to study internalization and subcellular localization of nanoparticles, does not allow unequivocal distinction between cell surface-bound and internalized particles, since there is no methodology to turn particles ‘off.’ We have developed a simple technique to rapidly remove silver nanoparticles outside living cells leaving only the internalized pool for imaging or quantification. The silver nanoparticle (AgNP) etching is based on the sensitivity of Ag to a hexacyanoferrate/thiosulfate redox-based destain solution. In demonstration of the technique we present a new class of multicolored plasmonic nanoprobes comprising dye-labeled AgNPs that are exceptionally bright and photostable, carry peptides as model targeting ligands, can be etched rapidly and with minimal toxicity in mice and that show tumour uptake in vivo.