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      Mechanisms of Selective Antitumor Action of Cold Atmospheric Plasma-Derived Reactive Oxygen and Nitrogen Species : Mechanisms of Selective Antitumor Action…

      1 , 2
      Plasma Processes and Polymers
      Wiley

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          Critical Review of rate constants for reactions of hydrated electronsChemical Kinetic Data Base for Combustion Chemistry. Part 3: Propane

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            Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide.

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              Cold plasma selectivity and the possibility of a paradigm shift in cancer therapy

              Background: Plasma is an ionised gas that is typically generated in high-temperature laboratory conditions. However, recent progress in atmospheric plasmas has led to the creation of cold plasmas with ion temperature close to room temperature. Methods: Both in-vitro and in-vivo studies revealed that cold plasmas selectively kill cancer cells. Results: We show that: (a) cold plasma application selectively eradicates cancer cells in vitro without damaging normal cells; and (b) significantly reduces tumour size in vivo. It is shown that reactive oxygen species metabolism and oxidative stress responsive genes are deregulated. Conclusion: The development of cold plasma tumour ablation has the potential of shifting the current paradigm of cancer treatment and enabling the transformation of cancer treatment technologies by utilisation of another state of matter.
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                Author and article information

                Journal
                Plasma Processes and Polymers
                Plasma Process Polym
                Wiley
                16128850
                December 2016
                December 2016
                October 14 2016
                : 13
                : 12
                : 1157-1178
                Affiliations
                [1 ]Institute of Virology, Medical Faculty; Medical Center-University of Freiburg; D-79104 Freiburg Germany
                [2 ]Department of Chemical and Biomolecular Engineering; University of California at Berkeley; Berkeley California 94720 USA
                Article
                10.1002/ppap.201600089
                53749c0b-8594-4260-80cc-540204f5afee
                © 2016

                http://doi.wiley.com/10.1002/tdm_license_1.1

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