Conductivity augments ROS and RNS delivery and tumor toxicity of an argon plasma jet.

Free Radic Biol Med

ZIK plasmatis, Leibniz Institute for Plasma Science and Technology (INP), a Member of the Leibniz Research Alliance Leibniz Health Technology, Felix-Hausdorff-Str. 2, 17489, Greifswald, Germany. Electronic address:

Published: February 2022

AI Article Synopsis

  • * A study comparing these two methods found that the direct contact (conducting) mode caused more cancer cell toxicity and inhibited tumor growth more effectively than the remote application of reactive species.
  • * The findings emphasize the need for standardized treatment distances in gas plasma therapies, which could guide clinicians in optimizing plasma-based cancer treatments in future.

Article Abstract

Gas plasma jet technology was recently identified as a potential adjuvant in the palliation of cancer patients. However, a practical point raised is if higher therapeutic efficacy is achieved with the gas plasma applied in direct contact to the tumor tissue (conducting) or during treatment with the remote cloud of reactive oxygen and nitrogen species (ROS/RNS) being expelled. In a bedside-to-bench study, this clinical question was translated into studying these two distinct treatment modalities using a three-dimensional tumor cell-matrix-hydrogel assay with subsequent quantitative confocal imaging. Z-resolved fluorescence analysis of two cancer cell lines revealed greater toxicity of the conducting mode. This result was re-iterated in the growth analysis of vascularized tumor tissue cultured on chicken embryos' CAM using in ovo bioluminescence imaging. Furthermore, for conducting compared to free mode, optical emission spectroscopy revealed stronger RNS signal lines in the gas phase, while both ROS/RNS deposition in the liquid was drastically exacerbated in the conducting mode. Altogether, our results are vital in understanding the importance of standardized treatment distances on the therapeutic efficacy of gas plasma exposure in clinical oncology and will help to give critical implications for clinicians involved in plasma onco-therapy in the future.

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http://dx.doi.org/10.1016/j.freeradbiomed.2022.01.014DOI Listing

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