| Literature DB >> 24161383 |
Cesare Achilli1, Stefania Grandi2, Annarita Ciana1, Gianni F Guidetti1, Alessandro Malara3, Vittorio Abbonante3, Laura Cansolino4, Corrado Tomasi5, Alessandra Balduini3, Maurizio Fagnoni2, Daniele Merli2, Piercarlo Mustarelli2, Ilaria Canobbio1, Cesare Balduini1, Giampaolo Minetti6.
Abstract
Boron neutron capture therapy (BNCT) is a radiotherapy treatment based on the accumulation in the tumor of a (10)B-containing drug and subsequent irradiation with low energy neutrons, which bring about the decay of (10)B to (7)Li and an α particle, causing the death of the neoplastic cell. The effectiveness of BNCT is limited by the low delivery and accumulation of the used boron-containing compounds. Here we report the development and the characterization of BPO4 nanoparticles (NPs) as a novel possible alternative drug for BNCT. An extensive analysis of BPO4 NP biocompatibility was performed using both mature blood cells (erythrocytes, neutrophils and platelets) and a model of hematopoietic progenitor cells. A time- and concentration-dependent cytotoxicity study was performed on neoplastic coloncarcinoma and osteosarcoma cell lines. BPO4 functionalization with folic acid, introduced to improve the uptake by tumor cells, appeared to effectively limit the unwanted effects of NPs on the analyzed blood components. FROM THE CLINICAL EDITOR: Boron neutron capture therapy (BNCT) is a radiotherapy treatment modality based on the accumulation of a (10)B-containing drug and subsequent irradiation with low energy neutrons, inducing the decay of (10)B to (7)Li and an α particle, causing neoplastic cell death. This team of authors reports on a folic acid functionalized BPO4 nanoparticle with improved characteristics compared with conventional BNCT approaches, as demonstrated in tumor cell lines, and hopefully to be followed by translational human studies.Entities:
Keywords: Blood cells; Boron-carrier; Cancer; Erythrocytes; Folic acid; Hemolysis; Nanomaterials; Neutrophils; Platelet aggregation
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Year: 2013 PMID: 24161383 DOI: 10.1016/j.nano.2013.10.003
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307