Literature DB >> 25947392

Identification of the biologically active liquid chemistry induced by a nonthermal atmospheric pressure plasma jet.

Kristian Wende1, Paul Williams2, Joe Dalluge3, Wouter Van Gaens4, Hamada Aboubakr5, John Bischof2, Thomas von Woedtke6, Sagar M Goyal7, Klaus-Dieter Weltmann6, Annemie Bogaerts4, Kai Masur8, Peter J Bruggeman2.   

Abstract

The mechanism of interaction of cold nonequilibrium plasma jets with mammalian cells in physiologic liquid is reported. The major biological active species produced by an argon RF plasma jet responsible for cell viability reduction are analyzed by experimental results obtained through physical, biological, and chemical diagnostics. This is complemented with chemical kinetics modeling of the plasma source to assess the dominant reactive gas phase species. Different plasma chemistries are obtained by changing the feed gas composition of the cold argon based RF plasma jet from argon, humidified argon (0.27%), to argon/oxygen (1%) and argon/air (1%) at constant power. A minimal consensus physiologic liquid was used, providing isotonic and isohydric conditions and nutrients but is devoid of scavengers or serum constituents. While argon and humidified argon plasma led to the creation of hydrogen peroxide dominated action on the mammalian cells, argon-oxygen and argon-air plasma created a very different biological action and was characterized by trace amounts of hydrogen peroxide only. In particular, for the argon-oxygen (1%), the authors observed a strong negative effect on mammalian cell proliferation and metabolism. This effect was distance dependent and showed a half life time of 30 min in a scavenger free physiologic buffer. Neither catalase and mannitol nor superoxide dismutase could rescue the cell proliferation rate. The strong distance dependency of the effect as well as the low water solubility rules out a major role for ozone and singlet oxygen but suggests a dominant role of atomic oxygen. Experimental results suggest that O reacts with chloride, yielding Cl2(-) or ClO(-). These chlorine species have a limited lifetime under physiologic conditions and therefore show a strong time dependent biological activity. The outcomes are compared with an argon MHz plasma jet (kinpen) to assess the differences between these (at least seemingly) similar plasma sources.

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Year:  2015        PMID: 25947392     DOI: 10.1116/1.4919710

Source DB:  PubMed          Journal:  Biointerphases        ISSN: 1559-4106            Impact factor:   2.456


  45 in total

1.  Aqueous Plasma Pharmacy: Preparation Methods, Chemistry, and Therapeutic Applications.

Authors:  Jessica M Joslin; James R McCall; Justin P Bzdek; Derek C Johnson; Brooks M Hybertson
Journal:  Plasma Med       Date:  2016

2.  Role of Ambient Gas Composition on Cold Physical Plasma-Elicited Cell Signaling in Keratinocytes.

Authors:  Anke Schmidt; Sander Bekeschus; Helena Jablonowski; Annemarie Barton; Klaus-Dieter Weltmann; Kristian Wende
Journal:  Biophys J       Date:  2017-06-06       Impact factor: 4.033

3.  The molecular chaperone Hsp33 is activated by atmospheric-pressure plasma protecting proteins from aggregation.

Authors:  Marco Krewing; Jennifer Janina Stepanek; Claudia Cremers; Jan-Wilm Lackmann; Britta Schubert; Alexandra Müller; Peter Awakowicz; Lars I O Leichert; Ursula Jakob; Julia E Bandow
Journal:  J R Soc Interface       Date:  2019-06-19       Impact factor: 4.118

4.  Plasma-sensitive Escherichia coli mutants reveal plasma resistance mechanisms.

Authors:  Marco Krewing; Fabian Jarzina; Tim Dirks; Britta Schubert; Jan Benedikt; Jan-Wilm Lackmann; Julia E Bandow
Journal:  J R Soc Interface       Date:  2019-03-29       Impact factor: 4.118

Review 5.  Cancer treatment with gas plasma and with gas plasma-activated liquid: positives, potentials and problems of clinical translation.

Authors:  Juliette C Harley; Natalka Suchowerska; David R McKenzie
Journal:  Biophys Rev       Date:  2020-08-05

6.  Reaction Chemistry Generated by Nanosecond Pulsed Dielectric Barrier Discharge Treatment is Responsible for the Tumor Eradication in the B16 Melanoma Mouse Model.

Authors:  Natalie Chernets; Deepa S Kurpad; Vitali Alexeev; Dario B Rodrigues; Theresa A Freeman
Journal:  Plasma Process Polym       Date:  2015-10-12       Impact factor: 3.872

7.  Stabilizing the cold plasma-stimulated medium by regulating medium's composition.

Authors:  Dayun Yan; Niki Nourmohammadi; Ka Bian; Ferid Murad; Jonathan H Sherman; Michael Keidar
Journal:  Sci Rep       Date:  2016-05-13       Impact factor: 4.379

Review 8.  Low temperature plasmas as emerging cancer therapeutics: the state of play and thoughts for the future.

Authors:  Adam M Hirst; Fiona M Frame; Manit Arya; Norman J Maitland; Deborah O'Connell
Journal:  Tumour Biol       Date:  2016-02-18

9.  Redox Stimulation of Human THP-1 Monocytes in Response to Cold Physical Plasma.

Authors:  Sander Bekeschus; Anke Schmidt; Lydia Bethge; Kai Masur; Thomas von Woedtke; Sybille Hasse; Kristian Wende
Journal:  Oxid Med Cell Longev       Date:  2015-11-15       Impact factor: 6.543

10.  Non-Thermal Plasma in Contact with Water: The Origin of Species.

Authors:  Yury Gorbanev; Deborah O'Connell; Victor Chechik
Journal:  Chemistry       Date:  2016-02-02       Impact factor: 5.236

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