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A 'tissue model' to study the plasma delivery of reactive oxygen species

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A 'tissue model' to study the plasma delivery of reactive oxygen species. / Szili, Endre J.; Bradley, James W.; Short, Robert D.
In: Journal of Physics D: Applied Physics, Vol. 47, No. 15, 152002, 16.04.2014.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Szili, EJ, Bradley, JW & Short, RD 2014, 'A 'tissue model' to study the plasma delivery of reactive oxygen species', Journal of Physics D: Applied Physics, vol. 47, no. 15, 152002. https://doi.org/10.1088/0022-3727/47/15/152002

APA

Szili, E. J., Bradley, J. W., & Short, R. D. (2014). A 'tissue model' to study the plasma delivery of reactive oxygen species. Journal of Physics D: Applied Physics, 47(15), Article 152002. https://doi.org/10.1088/0022-3727/47/15/152002

Vancouver

Szili EJ, Bradley JW, Short RD. A 'tissue model' to study the plasma delivery of reactive oxygen species. Journal of Physics D: Applied Physics. 2014 Apr 16;47(15):152002. Epub 2014 Mar 27. doi: 10.1088/0022-3727/47/15/152002

Author

Szili, Endre J. ; Bradley, James W. ; Short, Robert D. / A 'tissue model' to study the plasma delivery of reactive oxygen species. In: Journal of Physics D: Applied Physics. 2014 ; Vol. 47, No. 15.

Bibtex

@article{7ed8f006d0ad43368a2e4ad71a3e05a6,
title = "A 'tissue model' to study the plasma delivery of reactive oxygen species",
abstract = "We demonstrate the utility of a 'tissue model' to monitor the delivery of plasma jet-generated reactive oxygen species (ROS). We report on helium plasma jet interactions both across the surface and into the subsurface (defined as 150 mu m to 1.5 mm) of the tissue model. The model comprises a gelatin gel encapsulating a homogeneously dispersed chemical or biological reporter molecule. Jet-surface interactions result in (i) star shaped patterns that resemble those previously reported for surface-plasma streamers on insulators (as imaged by Pockels sensing) and (ii) 'filled' or hollow circular surface features, which resemble the 'killing' patterns seen in plasma jet treatments of bacterial lawns.The use of reporter molecules show that plasma can deliver ROS from 150 mu m to 1.5 mm below the tissue surface. Subsurface delivery of ROS is consistent with the use of plasma to decontaminate wounds (covered by wound exudate and clotted blood), the deactivation of whole biofilms, plasma-enhanced drug delivery through skin and the destruction of solid tumours.From the data presented, we argue that in these four cases (and others) ROS may be capable of directly accessing a tissue's subsurface, as opposed to other proposed mechanisms, which involve stimulating surface reactions that trigger a cascade of biomolecular signalling events (into the tissue).",
keywords = "plasma medicine, tissue model, reactive oxygen species, RANDOMIZED CONTROLLED-TRIAL, ATMOSPHERIC ARGON PLASMA, SURFACE-CHEMISTRY, ENERGY-TRANSFER, CANCER-THERAPY, CHRONIC WOUNDS, RADICALS, CELLS, ANGIOGENESIS, POLYMERS",
author = "Szili, {Endre J.} and Bradley, {James W.} and Short, {Robert D.}",
year = "2014",
month = apr,
day = "16",
doi = "10.1088/0022-3727/47/15/152002",
language = "English",
volume = "47",
journal = "Journal of Physics D: Applied Physics",
issn = "0022-3727",
publisher = "IOP Publishing Ltd",
number = "15",

}

RIS

TY - JOUR

T1 - A 'tissue model' to study the plasma delivery of reactive oxygen species

AU - Szili, Endre J.

AU - Bradley, James W.

AU - Short, Robert D.

PY - 2014/4/16

Y1 - 2014/4/16

N2 - We demonstrate the utility of a 'tissue model' to monitor the delivery of plasma jet-generated reactive oxygen species (ROS). We report on helium plasma jet interactions both across the surface and into the subsurface (defined as 150 mu m to 1.5 mm) of the tissue model. The model comprises a gelatin gel encapsulating a homogeneously dispersed chemical or biological reporter molecule. Jet-surface interactions result in (i) star shaped patterns that resemble those previously reported for surface-plasma streamers on insulators (as imaged by Pockels sensing) and (ii) 'filled' or hollow circular surface features, which resemble the 'killing' patterns seen in plasma jet treatments of bacterial lawns.The use of reporter molecules show that plasma can deliver ROS from 150 mu m to 1.5 mm below the tissue surface. Subsurface delivery of ROS is consistent with the use of plasma to decontaminate wounds (covered by wound exudate and clotted blood), the deactivation of whole biofilms, plasma-enhanced drug delivery through skin and the destruction of solid tumours.From the data presented, we argue that in these four cases (and others) ROS may be capable of directly accessing a tissue's subsurface, as opposed to other proposed mechanisms, which involve stimulating surface reactions that trigger a cascade of biomolecular signalling events (into the tissue).

AB - We demonstrate the utility of a 'tissue model' to monitor the delivery of plasma jet-generated reactive oxygen species (ROS). We report on helium plasma jet interactions both across the surface and into the subsurface (defined as 150 mu m to 1.5 mm) of the tissue model. The model comprises a gelatin gel encapsulating a homogeneously dispersed chemical or biological reporter molecule. Jet-surface interactions result in (i) star shaped patterns that resemble those previously reported for surface-plasma streamers on insulators (as imaged by Pockels sensing) and (ii) 'filled' or hollow circular surface features, which resemble the 'killing' patterns seen in plasma jet treatments of bacterial lawns.The use of reporter molecules show that plasma can deliver ROS from 150 mu m to 1.5 mm below the tissue surface. Subsurface delivery of ROS is consistent with the use of plasma to decontaminate wounds (covered by wound exudate and clotted blood), the deactivation of whole biofilms, plasma-enhanced drug delivery through skin and the destruction of solid tumours.From the data presented, we argue that in these four cases (and others) ROS may be capable of directly accessing a tissue's subsurface, as opposed to other proposed mechanisms, which involve stimulating surface reactions that trigger a cascade of biomolecular signalling events (into the tissue).

KW - plasma medicine

KW - tissue model

KW - reactive oxygen species

KW - RANDOMIZED CONTROLLED-TRIAL

KW - ATMOSPHERIC ARGON PLASMA

KW - SURFACE-CHEMISTRY

KW - ENERGY-TRANSFER

KW - CANCER-THERAPY

KW - CHRONIC WOUNDS

KW - RADICALS

KW - CELLS

KW - ANGIOGENESIS

KW - POLYMERS

U2 - 10.1088/0022-3727/47/15/152002

DO - 10.1088/0022-3727/47/15/152002

M3 - Journal article

VL - 47

JO - Journal of Physics D: Applied Physics

JF - Journal of Physics D: Applied Physics

SN - 0022-3727

IS - 15

M1 - 152002

ER -