Cubosomes and Hexosomes in Theranostic Nanomedicine

Sergio Murgia 1 Claudia Caltagirone 1 Angela M. Falchi 2 Valeria Meli 1 Maura Monduzzi 1 Luca Prodi 3 Judith Schmidt 4 Yeshayahu Talmon 4
1Department of Chemical and Geological Science, University of Cagliari, Monserrato (CA), Italy
2Department of Biomedical Science, University of Cagliari, Monserrato (CA), Italy
3Department of Chemistry "G. Ciamician", University of Bologna, Bologna, Italy
4Department of Chemical Engineering, Technion, Israel Institute of Technology, Haifa, Israel

Application of nanotechnology to medicine offers a versatile approach for the design and the development of new multi-functional drug delivery systems where imaging probes, drugs, and targeting agents can be combined and applied as therapeutic/diagnostic (theranostic) tools. Furthermore, this application requires the development of biocompatible and non-toxic systems with tunable properties. In this context, lipid-based nanoparticles seem to be flexible platforms, since they can be personalized depending on their application.

Here, two types of nanoparticles based on a biocompatible lipid (monoolein), respectively known as cubosomes and hexosomes, are proposed as theranostic platforms for cancer treatment. Both these nanoparticles show high mechanical rigidity and structural stability and, because of their intrinsic nanostructure, can be loaded with hydrophobic or hydrophilic cargos. It will be shown that cubosomes and hexosomes can effectively be loaded with anticancer drugs, UV-visible or NIR emitting fluorophores, while simultaneously conjugated with cancer cells-targeting ligands. Their living cells imaging skills and addressing abilities toward HeLa cells will be also presented.

 
 
 

Figure. (A) Cubosome nanoparticle loaded with quercetin and prepared with dansyl-conjugated F108 Pluronic. (B) Fluorescence image of viable 3T3 fibroblast cells after treatment with cubosomes loaded with hydrophobically modified fluorescein.

Reference: S. Murgia, S. Bonacchi, A. M. Falchi, S. Lampis, V. Lippolis, V. Meli, M. Monduzzi, L. Prodi, J. Schmidt, Y. Talmon, C. Caltagirone, Langmuir, 2013, 29, 6673

 

murgias@unica.it








 




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