Polyinosinic-polycytidylic acid (poly(I:C)) is a synthetic double-stranded RNA (dsRNA) analog able to induce apoptosis in different cancer cells by the activation of toll-like receptor 3 (TLR3) and cytosolic helicases, retinoic acid inducible gene I (RIG-I) like receptors. In this work, we have synthesized and thoroughly characterized a core-shell liposome-silica hybrid (LSH) nanoparticle (NP) made of a silica core surrounded by a multicomponent cationic lipid bilayer. In view of in vivo applications, a variant with polyethyleneglycol (PEG) grafted onto the lipid surface was also synthesized. Poly(I:C)-loaded LSH NPs were characterized and optimized in terms of their chemical-physical properties by using dynamic light scattering (DLS), micro-electrophoresis and transmission electron microscopy (TEM). The ability of this new technology to kill cancer cells was validated in PC3 prostate cancer and MCF7 breast cancer cells by MTT proliferation assay, flow cytometry and fluorescence confocal microscopy. We found that negatively charged poly(I:C)-loaded LSH NPs are more efficient than their liposome counterpart in eliminating cancer cells, thus representing excellent candidates for both in vitro and in vivo drug delivery applications.

Killing cancer cells using nanotechnology: novel poly(I:C) loaded liposome-silica hybrid nanoparticles / Colapicchioni, Valentina; Palchetti, Sara; Pozzi, Daniela; Marini, ELETTRA SARA; Riccioli, Anna; Ziparo, Elio; Papi, Massimiliano; Amenitsch, Heinz; Caracciolo, Giulio. - In: JOURNAL OF MATERIALS CHEMISTRY. B. - ISSN 2050-750X. - ELETTRONICO. - 3:37(2015), pp. 7408-7416. [10.1039/c5tb01383f]

Killing cancer cells using nanotechnology: novel poly(I:C) loaded liposome-silica hybrid nanoparticles

PALCHETTI, SARA;POZZI, DANIELA;RICCIOLI, ANNA;CARACCIOLO, Giulio
2015

Abstract

Polyinosinic-polycytidylic acid (poly(I:C)) is a synthetic double-stranded RNA (dsRNA) analog able to induce apoptosis in different cancer cells by the activation of toll-like receptor 3 (TLR3) and cytosolic helicases, retinoic acid inducible gene I (RIG-I) like receptors. In this work, we have synthesized and thoroughly characterized a core-shell liposome-silica hybrid (LSH) nanoparticle (NP) made of a silica core surrounded by a multicomponent cationic lipid bilayer. In view of in vivo applications, a variant with polyethyleneglycol (PEG) grafted onto the lipid surface was also synthesized. Poly(I:C)-loaded LSH NPs were characterized and optimized in terms of their chemical-physical properties by using dynamic light scattering (DLS), micro-electrophoresis and transmission electron microscopy (TEM). The ability of this new technology to kill cancer cells was validated in PC3 prostate cancer and MCF7 breast cancer cells by MTT proliferation assay, flow cytometry and fluorescence confocal microscopy. We found that negatively charged poly(I:C)-loaded LSH NPs are more efficient than their liposome counterpart in eliminating cancer cells, thus representing excellent candidates for both in vitro and in vivo drug delivery applications.
2015
biomedical engineering; medicine (all); chemistry (all); materials science (all)
01 Pubblicazione su rivista::01a Articolo in rivista
Killing cancer cells using nanotechnology: novel poly(I:C) loaded liposome-silica hybrid nanoparticles / Colapicchioni, Valentina; Palchetti, Sara; Pozzi, Daniela; Marini, ELETTRA SARA; Riccioli, Anna; Ziparo, Elio; Papi, Massimiliano; Amenitsch, Heinz; Caracciolo, Giulio. - In: JOURNAL OF MATERIALS CHEMISTRY. B. - ISSN 2050-750X. - ELETTRONICO. - 3:37(2015), pp. 7408-7416. [10.1039/c5tb01383f]
File allegati a questo prodotto
File Dimensione Formato  
Colapicchioni_Killing-cancer-cells_2015.pdf

solo gestori archivio

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 3.31 MB
Formato Adobe PDF
3.31 MB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/840126
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 32
  • ???jsp.display-item.citation.isi??? 25
social impact