Synergistic effects of nanosecond pulsed plasma and electric field on inactivation of pancreatic cancer cells in vitro

Author:

Oshin Edwin A.1,Minhas Zobia1,Biancatelli Ruben M. L. Colunga1,Catravas John D.1,Heller Richard2,Guo Siqi1,Jiang Chunqi1

Affiliation:

1. Old Dominion University

2. University of South Florida

Abstract

Abstract Nanosecond pulsed atmospheric pressure plasma jets (ns-APPJs) produce reactive plasma species, including charged particles and reactive oxygen and nitrogen species (RONS), which can induce oxidative stress in biological cells. Nanosecond pulsed electric field (nsPEF) has also been found to cause permeabilization of cell membranes and induce apoptosis or cell death. Combining the treatment of ns-APPJ and nsPEF may enhance the effectiveness of cancer cell inactivation with only moderate doses of both treatments. Employing ns-APPJ powered by 9 kV, 200 ns pulses at 2 kHz and 60-nsPEF of 50 kV/cm at 1 Hz, the synergistic effects on pancreatic cancer cells (Pan02) in vitro were evaluated on cell viability and transcellular electrical resistance (TER). It was observed that treatment with ns-APPJ for > 2 min disrupts Pan02 cell stability and resulted in over 30% cell death. Similarly, applying nsPEF alone, > 20 pulses resulted in over 15% cell death. While the inactivation activity from the individual treatment is moderate, combined treatments resulted in 80% cell death, approximately 3-to-5-fold increase compared to the individual treatment. In addition, reactive oxygen species such as OH and O were identified at the plasma-liquid interface. The gas temperature of the plasma and the temperature of the cell solution during treatments were determined to be near room temperature. * Work supported in part by the National Institutes of Health (NIH) under award number 1R01EB023878-01A1 and the Air Force Office of Scientific Research of the United States of America (AFOSR) under award number FA9550-22-1-0115 and FA9550-22-1-0428. The funders had no role in study design, collection of data, decision to publish, or in preparation of this manuscript. In addition, effort of ZM and SG are supported by the Old Dominion University Multi-disciplinary Biomedical Research Seed Fund.

Publisher

Research Square Platform LLC

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