Literature DB >> 24161383

Biocompatibility of functionalized boron phosphate (BPO4) nanoparticles for boron neutron capture therapy (BNCT) application.

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.
© 2014.

Entities:  

Keywords:  Blood cells; Boron-carrier; Cancer; Erythrocytes; Folic acid; Hemolysis; Nanomaterials; Neutrophils; Platelet aggregation

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Substances:

Year:  2013        PMID: 24161383     DOI: 10.1016/j.nano.2013.10.003

Source DB:  PubMed          Journal:  Nanomedicine        ISSN: 1549-9634            Impact factor:   5.307


  6 in total

Review 1.  Advancements in Tumor Targeting Strategies for Boron Neutron Capture Therapy.

Authors:  Micah John Luderer; Pilar de la Puente; Abdel Kareem Azab
Journal:  Pharm Res       Date:  2015-06-02       Impact factor: 4.200

2.  Amyloid-beta (25-35) peptide induces the release of pro-matrix metalloprotease 9 (pro-MMP-9) from human neutrophils.

Authors:  Cesare Achilli; Annarita Ciana; Giampaolo Minetti
Journal:  Mol Cell Biochem       Date:  2014-08-03       Impact factor: 3.396

Review 3.  Action of Nanoparticles on Platelet Activation and Plasmatic Coagulation.

Authors:  Eleonore Fröhlich
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

4.  Cyclic-RGDyC functionalized liposomes for dual-targeting of tumor vasculature and cancer cells in glioblastoma: An in vitro boron neutron capture therapy study.

Authors:  Weirong Kang; Darren Svirskis; Vijayalekshmi Sarojini; Ailsa L McGregor; Joseph Bevitt; Zimei Wu
Journal:  Oncotarget       Date:  2017-05-30

Review 5.  Boron delivery agents for neutron capture therapy of cancer.

Authors:  Rolf F Barth; Peng Mi; Weilian Yang
Journal:  Cancer Commun (Lond)       Date:  2018-06-19

6.  Water-Soluble closo-Docecaborate-Containing Pteroyl Derivatives Targeting Folate Receptor-Positive Tumors for Boron Neutron Capture Therapy.

Authors:  Fumiko Nakagawa; Hidehisa Kawashima; Taiki Morita; Hiroyuki Nakamura
Journal:  Cells       Date:  2020-07-03       Impact factor: 6.600

  6 in total

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