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Radiobiological Implications of Nanoparticles Following Radiation Treatment

Reem Ahmad, Giuseppe Schettino, Gary Royle, Miriam Barry, Quentin A. Pankhurst, Olivier Tillement, Ben Russell, Kate Ricketts

2020Particle & Particle Systems Characterization28 citationsDOIOpen Access PDF

Abstract

Abstract Materials with a high atomic number (Z) are shown to cause an increase in the level of cell kill by ionizing radiation when introduced into tumor cells. This study uses in vitro experiments to investigate the differences in radiosensitization between two cell lines (MCF‐7 and U87) and three commercially available nanoparticles (gold, gadolinium, and iron oxide) irradiated by 6 MV X‐rays. To assess cell survival, clonogenic assays are carried out for all variables considered, with a concentration of 0.5 mg mL −1 for each nanoparticle material used. This study demonstrates differences in cell survival between nanoparticles and cell line. U87 shows the greatest enhancement with gadolinium nanoparticles (2.02 ± 0.36), whereas MCF‐7 cells have higher enhancement with gold nanoparticles (1.74 ± 0.08). Mass spectrometry, however, shows highest elemental uptake with iron oxide and U87 cells with 4.95 ± 0.82 pg of iron oxide per cell. A complex relationship between cellular elemental uptake is demonstrated, highlighting an inverse correlation with the enhancement, but a positive relation with DNA damage when comparing the same nanoparticle between the two cell lines.

Topics & Concepts

NanoparticleClonogenic assayIonizing radiationChemistryIron oxide nanoparticlesCell cultureGadoliniumIrradiationRadiochemistryIron oxideIn vitroU87CellBiophysicsNanotechnologyMaterials scienceBiochemistryBiologyGeneticsNuclear physicsPhysicsOrganic chemistryRadiation Therapy and DosimetryRadiation Shielding Materials AnalysisEffects of Radiation Exposure
Radiobiological Implications of Nanoparticles Following Radiation Treatment | Litcius