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/ Health News / 2008 / May 2008 / May 15, 2008 Carbon-coated nanomagnets could serve as potential hyperthermia agents |
How cancer prevention drives aging
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A new research has suggested that carbon-coated nanomagnets could serve as a safe and effective hyperthermia agent, targeting and destroying cancerous cells.
Washington, May 15 : A new research has suggested that carbon-coated nanomagnets could serve as a safe and effective hyperthermia agent, targeting and destroying cancerous cells.
Researchers from Germany found that nanoparticles consisting of metallic iron with a protective carbon coat could be potential hyperthermia agents.
In animal models, using heat to selectively kill tumor cells has proven efficient.
Using metallic iron in the nanoparticles (in lieu of iron oxide) would allow heating at greater temperatures; and coating the iron with carbon would prevent the iron from rusting, which can hinder the effectiveness of the therapy.
In order to ensure that the nanoparticles did not harm non-cancerous cells, researchers tested their compatibility with normal tissues. Human PC-3 prostate cells and a non-malignant fibroblast cell line were incubated with the carbon coated nanomagnets and, after the incubation period, the cells did not experience major cytotoxic (cell-destroying) effects.
The cell cycle distribution and the apoptosis rate were not impaired by the presence of nanomagnets, reflecting the biocompatible character of these structures.
This breakthrough could provide an effective treatment option for many types of cancer, without the destruction of surrounding cells associated with chemotherapy or invasive surgery, the researchers said.
The fact that the carbon-coating prevented cell destruction during incubation proves that the nanoparticles could potentially serve as safe and effective hyperthermia agents, targeting and destroying cancerous cells.
These findings underscore a need for more research regarding the use of nanoparticles as potential cancer treatments.
The study was presented at the 103rd Annual Scientific Meeting of the American Urological Association.
ANI