The antibacterial and cell-proliferative
character of atmospheric
pressure plasma jets (APPJs) helps in the healing process of chronic
wounds. However, control of the plasma-biological target interface
remains an open issue. High vacuum ultraviolet/ultraviolet (VUV/UV)
radiation and RONS flux from plasma may cause damage of a treated
tissue; therefore, controlled interaction is essential. VUV/UV emission
from argon APPJs and radiation control with aerosol injection in plasma
effluent is the focus of this research. The aerosol effect on radiation
is studied by a fluorescent target capable of resolving the plasma
oxidation footprint. In addition, DNA damage is evaluated by plasmid
DNA radiation assay and cell proliferation assay to assess safety
aspects of the plasma jet, the effect of VUV/UV radiation, and its
control with aerosol injection. Inevitable emission of VUV/UV radiation
from plasmas during treatment is demonstrated in this work. Plasma
has no antiproliferative effect on fibroblasts in short treatments
(t < 60 s), while long exposure has a cytotoxic
effect, resulting in decreased cell survival. Radiation has no effect
on cell survival in the medium due to absorption. However, a strong
cytotoxic effect on the attached fibroblasts without the medium is
apparent. VUV/UV radiation contributes 70% of the integral plasma
effect in induction of single- and double-strand DNA breaks and cytotoxicity
of the attached cells without the medium. Survival of the attached
cells increases by 10% when aerosol is introduced between plasma and
the cells. Injection of aerosol in the plasma effluent can help to
control the plasma–cell/tissue interaction. Aerosol droplets
in the effluent partially absorb UV emission from the plasma, limiting
photon flux in the direction of the biological target. Herein, cold
and safe plasma-aerosol treatment and a safe operational mode of treatment
are demonstrated in a murine model.