4.5 Article

An experimental burn wound-healing study of non-thermal atmospheric pressure microplasma jet arrays

Journal

Publisher

WILEY-BLACKWELL
DOI: 10.1002/term.2074

Keywords

non-thermal; microplasma; burn; wound; biomedical; device

Funding

  1. Hallym University Research Fund
  2. National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [2013R1A1A2074849]
  3. US Air Force Office of Scientific Research [FA9550-14-1-0146]
  4. National Research Foundation of Korea [2013R1A1A2074849] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In contrast with a thermal plasma surgical instrument based on coagulative and ablative properties, low-temperature (non-thermal) non-equilibrium plasmas are known for novel medicinal effects on exposed tissue while minimizing undesirable tissue damage. In this study we demonstrated that arrays of non-thermal microplasma jet devices fabricated from a transparent polymer can efficiently inactivate fungi (Candida albicans) as well as bacteria (Escherichia coli), both in vitro and in vivo, and that this leads to a significant wound-healing effect. Microplasma jet arrays offer several advantages over conventional single-jet devices, including superior packing density, inherent scalability for larger treatment areas, unprecedented material flexibility in a plasma jet device, and the selective generation of medically relevant reactive species at higher plasma densities. The therapeutic effects of our multi-jet device were verified on second-degree burns in animal rat models. Reduction of the wound area and the histology of the wound after treatment have been investigated, and expression of interleukin (IL)-1, -6 and -10 was verified to evaluate the healing effects. The consistent effectiveness of non-thermal plasma treatment has been observed especially in decreasing wound size and promoting re-epithelialization through collagen arrangement and the regulation of expression of inflammatory genes. Copyright (c) 2015 John Wiley & Sons, Ltd.

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