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Targeting FR-expressing cells in ovarian cancer with Fab-functionalized nanoparticles: a full study to provide the proof of principle from in vitroto in vivo

Efficient targeting in tumor therapies is still an open issue: systemic biodistribution and poor specific accumulation of drugs weaken efficacy of treatments. Engineered nanoparticles are expected to bring benefits by allowing specific delivery of drug to the tumor or acting themselves as localized...

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Bibliographic Details
Published in:Nanoscale 2015-01, Vol.7 (6), p.2336-2351
Main Authors: Quarta, Alessandra, Bernareggi, Davide, Benigni, Fabio, Luison, Elena, Nano, Giuseppe, Nitti, Simone, Cesta, Maria Candida, Di Ciccio, Luciano, Canevari, Silvana, Pellegrino, Teresa, Figini, Mariangela
Format: Article
Language:English
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Summary:Efficient targeting in tumor therapies is still an open issue: systemic biodistribution and poor specific accumulation of drugs weaken efficacy of treatments. Engineered nanoparticles are expected to bring benefits by allowing specific delivery of drug to the tumor or acting themselves as localized therapeutic agents. In this study we have targeted epithelial ovarian cancer with inorganic nanoparticles conjugated to a human antibody fragment against the folate receptor over-expressed on cancer cells. The conjugation approach is generally applicable. Indeed several types of nanoparticles (either magnetic or fluorescent) were engineered with the fragment, and their biological activity was preserved as demonstrated by biochemical methods in vitro. In vivostudies with mice bearing orthotopic and subcutaneous tumors were performed. Elemental and histological analyses showed that the conjugated magnetic nanoparticles accumulated specifically and were retained at tumor sites longer than the non-conjugated nanoparticles.
ISSN:2040-3364
2040-3372
DOI:10.1039/c4nr04426f