4.3 Article

Bifunctional Magnetite-Gold Nanoparticles for Magneto-Mechanical Actuation and Cancer Cell Destruction

期刊

MAGNETOCHEMISTRY
卷 8, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/magnetochemistry8120185

关键词

magnetite-gold dumbbell nanoparticles; low-frequency magnetic field; biomedical application; prostate cancer cells; cancer cell destruction; SICM

资金

  1. Russian Science Foundation [21-74-20077, 22-19-00824]

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This study investigated the remote manipulation of Fe3O4-Au hybrid particles in different magnetic fields and demonstrated their aggregation and disaggregation behavior in aqueous solution. Additionally, the study found that these particles have potential applications in cancer therapy based on their uptake by cancer cells and their effect on cell viability.
Magnetite-gold dumbbell nanoparticles are essential for biomedical applications due to the presence of two surfaces with different chemical natures and the potential combination of magnetic and plasmonic properties. Here, the remote actuation of Fe3O4-Au hybrid particles in a rotating (1 Hz, 7 mT), static (7 mT) or pulsed low-frequency (31 Hz, 175 mT, 30 s pulse/30 s pause) magnetic field was studied. The particles were synthesized by a high-temperature wet chemistry protocol and exhibited superparamagnetic properties with the saturation magnetization of 67.9 +/- 3.0 Am-2 kg(-1). We showcased the nanoparticles' controlled aggregation in chains (rotating/static magnetic field) in an aqueous solution and their disaggregation when the field was removed. The investigation of nanoparticle uptake by LNCaP and PC-3 cancer cells demonstrated that Fe3O4-Au hybrids mainly escaped endosomes and accumulated in the cytoplasm. A significant fraction of them still responded to a rotating magnetic field, forming short chains. The particles were not toxic to cells at concentrations up to 210 mu g (Fe3O4) mL(-1). However, cell viability decrease after incubation with the nanoparticles (>= 70 mu g mL(-1)) and exposure to a pulsed low-frequency magnetic field was found. We ascribe this effect to mechanically induced cell destruction. Overall, this makes Fe3O4-Au nanostructures promising candidates for intracellular actuation for future magneto-mechanical cancer therapies.

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