Abstract

Many studies have focused on the possibility of applying graphene oxide as an effective drug delivery system, but also as an effective tool for a thermally-responsive system. Thus, the main aim of the study was to evaluate the cellular response of the MCF-7 cell line to covalently and non-covalently conjugated graphene oxide with hydroxycamptothecin (GO-HCPT) and the effect of an 8-h rotating magnetic field (RMF) exposure. The objective of this novel approach is to use graphene oxide platform not only as a drug delivery system, but also as an effective tool for a thermally-responsive system. The present study analyzed the effect of nanocomposites and RMF on the activity of MCF-7 cells and revealed that mitochondrial metabolism was significantly reduced in the cells incubated under all tested RMF parameters. In all tested variants of c-GO-HCPT concentrations and RMF inductions, cell viability was reduced by approximately 10–50% (data from WST-1 assay) for cells incubated with nanocomposite for 24 h and 70–90% for cells incubated with nanocomposite for 48 h. The observed LDH leakage was higher for cells exposed to c-GO-HCPT for longer incubation time. In the case of nc-GO-HCPT, the relative viability was reduced by 10–30%, respectively to the sample concentration and magnetic induction value for 48-h incubation. The data obtained in the NR assays after 24 h confirmed slightly higher cytotoxic co-effect of nc-GO-HCPT with cellular metabolism reduced by 90–98%. The concentration of nanomaterials also influenced mitochondrial metabolism. Both tested nanomaterials, c-GO-HCPT and nc-GO-HCPT, and RMF affected effectively the metabolism and viability of the cells, but not in a dose-dependent manner. A small difference in cellular response was observed in the presence of non-covalent and covalent GO-HCPT, with a slightly higher cytotoxicity effect of nc-GO-HCPT, visible 24 h after the experiment. These findings could have potential clinical application, including targeted tumor chemotherapy and thermal ablation.

Full Text
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