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dc.contributor.authorRowe, Warren
dc.contributor.authorCheng, Xiaoqian
dc.contributor.authorLy, Lawan
dc.contributor.authorZhuang, Taisen
dc.contributor.authorBasadonna, Giacomo
dc.contributor.authorTrink, Barry
dc.contributor.authorKeidar, Michael
dc.contributor.authorCanady, Jerome
dc.date2022-08-11T08:09:51.000
dc.date.accessioned2022-08-23T16:45:57Z
dc.date.available2022-08-23T16:45:57Z
dc.date.issued2018-09-07
dc.date.submitted2018-11-01
dc.identifier.citation<p>Rowe, W.; Cheng, X.; Ly, L.; Zhuang, T.; Basadonna, G.; Trink, B.; Keidar, M.; Canady, J. The Canady Helios Cold Plasma Scalpel Significantly Decreases Viability in Malignant Solid Tumor Cells in a Dose-Dependent Manner. Plasma 2018, 1, 177-188.<em> </em> <a href="https://doi.org/10.3390/plasma1010016">https://doi.org/10.3390/plasma1010016</a></p>
dc.identifier.doi10.3390/plasma1010016
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40784
dc.description.abstractTo determine appropriate treatment doses of cold atmospheric plasma (CAP), the Canady Helios Cold Plasma Scalpel was tested across numerous cancer cell types including renal adenocarcinoma, colorectal carcinoma, pancreatic adenocarcinoma, ovarian adenocarcinoma, and esophageal adenocarcinoma. Various CAP doses were tested consisting of both high (3 L/min) and low (1 L/min) helium flow rates, several power settings, and a range of treatment times up to 5 min. The impact of cold plasma on the reduction of viability was consistently dose-dependent; however, the anti-cancer capability varied significantly between cell lines. While the lowest effective dose varied from cell line to cell line, in each case an 80–99% reduction in viability was achievable 48 h after CAP treatment. Therefore, it is critical to select the appropriate CAP dose necessary for treating a specific cancer cell type.
dc.language.isoen_US
dc.rights© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectcold atmospheric plasma
dc.subjectCAP
dc.subjectcancer therapy
dc.subjectdose-dependent
dc.subjectrenal adenocarcinoma
dc.subjectcolorectal carcinoma
dc.subjectpancreatic adenocarcinoma
dc.subjectovarian adenocarcinoma
dc.subjectesophageal adenocarcinoma
dc.subjectBiotechnology
dc.subjectCancer Biology
dc.subjectCells
dc.subjectEquipment and Supplies
dc.subjectNeoplasms
dc.subjectSurgical Procedures, Operative
dc.subjectTherapeutics
dc.titleThe Canady Helios Cold Plasma Scalpel Significantly Decreases Viability in Malignant Solid Tumor Cells in a Dose-Dependent Manner
dc.typeJournal Article
dc.source.journaltitlePlasma
dc.source.volume2018
dc.source.issue1
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4604&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3593
dc.identifier.contextkey13222369
refterms.dateFOA2022-08-23T16:45:57Z
html.description.abstract<p>To determine appropriate treatment doses of cold atmospheric plasma (CAP), the Canady Helios Cold Plasma Scalpel was tested across numerous cancer cell types including renal adenocarcinoma, colorectal carcinoma, pancreatic adenocarcinoma, ovarian adenocarcinoma, and esophageal adenocarcinoma. Various CAP doses were tested consisting of both high (3 L/min) and low (1 L/min) helium flow rates, several power settings, and a range of treatment times up to 5 min. The impact of cold plasma on the reduction of viability was consistently dose-dependent; however, the anti-cancer capability varied significantly between cell lines. While the lowest effective dose varied from cell line to cell line, in each case an 80–99% reduction in viability was achievable 48 h after CAP treatment. Therefore, it is critical to select the appropriate CAP dose necessary for treating a specific cancer cell type.</p>
dc.identifier.submissionpathoapubs/3593
dc.contributor.departmentDepartment of Surgery
dc.source.pages177-188


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© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
Except where otherwise noted, this item's license is described as © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).