One Year Follow-Up Risk Assessment in SKH-1 Mice and Wounds Treated with an Argon Plasma Jet

dc.bibliographicCitation.firstPage868
dc.bibliographicCitation.issue4
dc.bibliographicCitation.journalTitleInternational journal of molecular scienceseng
dc.bibliographicCitation.volume18
dc.contributor.authorSchmidt, Anke
dc.contributor.authorvon Woedtke, Thomas
dc.contributor.authorStenzel, Jan
dc.contributor.authorLindner, Tobias
dc.contributor.authorPolei, Stefan
dc.contributor.authorVollmar, Brigitte
dc.contributor.authorBekeschus, Sander
dc.date.accessioned2023-01-10T10:44:19Z
dc.date.available2023-01-10T10:44:19Z
dc.date.issued2017-4-19
dc.description.abstractMultiple evidence in animal models and in humans suggest a beneficial role of cold physical plasma in wound treatment. Yet, risk assessment studies are important to further foster therapeutic advancement and acceptance of cold plasma in clinics. Accordingly, we investigated the long-term side effects of repetitive plasma treatment over 14 consecutive days in a rodent full-thickness ear wound model. Subsequently, animals were housed for 350 days and sacrificed thereafter. In blood, systemic changes of the pro-inflammatory cytokines interleukin 1β and tumor necrosis factor α were absent. Similarly, tumor marker levels of α-fetoprotein and calcitonin remained unchanged. Using quantitative PCR, the expression levels of several cytokines and tumor markers in liver, lung, and skin were found to be similar in the control and treatment group as well. Likewise, histological and immunohistochemical analysis failed to detect abnormal morphological changes and the presence of tumor markers such as carcinoembryonic antigen, α-fetoprotein, or the neighbor of Punc 11. Absence of neoplastic lesions was confirmed by non-invasive imaging methods such as anatomical magnetic resonance imaging and positron emission tomography-computed tomography. Our results suggest that the beneficial effects of cold plasma in wound healing come without apparent side effects including tumor formation or chronic inflammation.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10817
dc.identifier.urihttp://dx.doi.org/10.34657/9843
dc.language.isoeng
dc.publisherBasel : Molecular Diversity Preservation International
dc.relation.doihttps://doi.org/10.3390/ijms18040868
dc.relation.essn1422-0067
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc570
dc.subject.ddc540
dc.subject.otherDermal full-thickness woundseng
dc.subject.otherKINPen plasma jeteng
dc.subject.otherPlasma medicineeng
dc.subject.otherReactive oxygen and nitrogen specieseng
dc.subject.otherRisk evaluationeng
dc.subject.otherSKH1 mouse modeleng
dc.titleOne Year Follow-Up Risk Assessment in SKH-1 Mice and Wounds Treated with an Argon Plasma Jeteng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorINP
wgl.subjectBiowissenschaften/Biologieger
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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