Abstract
The efficacy of the plasma pencil is studied for its cancer therapeutics effects against the SCaBER cell line. First, the SCaBER cells in media were treated with different exposure times of low temperature plasma (LTP). Secondly, LTP activated media was generated by treating the media prior to adding it to the cells. Cell viability was assayed at 0, 24, 48, and 72 h after treatments. The results indicate that both treatments alter cell morphology, cell reattachment, and kill SCaBER cells in an exposure time dependent and delayed manner. Caspase‐3 assays reveal that plasma can activate the cells' apoptotic pathways.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
