International Journal of Hyperthermia · 2014 · 77 citations · 22 references
Life SciencesCell BiologyOncologyApoptosisBiophotonicsNanomaterialsCancer NanomedicineCell-nanoparticle InteractionsHeat InjuryNanomedicineNanotoxicologyPhotothermal TherapyCancer Photothermal TherapyCell Death AssaysHeat GenerationHyperthermiaNanomaterial Cytotoxicity AssessmentNanoparticle-induced CytotoxicityNanoparticlesPhotothermal Effects
PURPOSE: Silver nanoparticles (Ag NP) can generate heat upon exposure to infrared light. The in vitro response of breast cell lines to Ag NP, both with and without nanoparticle-induced heating was evaluated. MATERIALS AND METHODS: Ag NP heat generation, intracellular silver concentration, and cell viability of MDA-MB-231, MCF7, and MCF 10A breast cells with Ag NP alone, or after exposure to 0.79 or 2.94 W/cm2 of 800 nm light were evaluated. RESULTS: The concentration of Ag NP to induce sufficient heat for cell death, upon exposure to 800 nm light, was 5-250 μg/mL. Clonogenics assay indicates a cytotoxic response of MCF7 (45% decrease) and MDA-MB-231 (80% decrease) cells to 10 µg/mL, whereas MCF 10A had a 25% increase. Without Ag NP, MDA-MB-231 cells were more susceptible to hyperthermia, compared to MCF7 and MCF 10A cells. Clonogenics assay of Ag NP-induced photothermal ablation demonstrated that MCF 10A cells have the highest survival fraction. MCF7 cells had more silver in the cytoplasm, MDA-MB-231 cells had more in the nuclei, and MCF 10A cells had equivalent concentrations in the cytoplasm and nuclei. CONCLUSIONS: Ag NP are effective photothermal agents. A secondary benefit is the differential response of breast cancer cells to Ag NP-induced hyperthermia, due to increased intracellular silver content, compared to non-tumorigenic breast epithelial cells.
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Natural Sciences, Biomedical Engineering, Materials Science +17
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