• J D Iljas, J Röhl, J A McGovern, K H Moromizato, T J Parker, and L Cuttle.
• Queensland University of Technology (QUT), Tissue Repair and Translational Physiology Program, Institute of Health and Biomedical Innovation, Brisbane, Queensland, Australia; The University of Queensland, The Christopher Chen Oocyte Biology Research Laboratory, Centre for Clinical Research, Brisbane, Queensland, Australia.
• Burns. 2021 Mar 1; 47 (2): 417-429.

AbstractIn this study, a deep burn wound model was established using a 3D human skin equivalent (HSE) model and this was compared to native skin. HSEs were constructed from dermis derived from abdominoplasty/breast surgery and this dermal template was seeded with primary keratinocytes and fibroblasts. The HSE model was structurally similar to native skin with a stratified and differentiated epidermis. A contact burn (60 °C, 80 °C, 90 °C) was applied with a modified soldering iron and wounds were observed at day 1 and 7 after burn. The HSEs demonstrated re-growth with keratinocyte proliferation and formation of a neo-epidermis after burn injury, whereas the ex vivo native skin did not. To assess the suitability of the 3D HSE model for penetration and toxicity studies, a nanocrystalline silver dressing was applied to the model for 7 days, with and without burn injury. The effect of silver on skin re-growth and its penetration and subcellular localization was assessed in HSEs histologically and with laser ablation-inductively coupled plasma mass spectrometry (LA-ICPMS). The silver treatment delayed or reduced skin re-growth, and silver particles were detected on the top of the epidermis, and within the papillary dermis. This novel in vitro 3D multicellular deep burn wound model is effective for studying the pathology and treatment of burn wound injury and is suitable for penetration and toxicity studies of wound healing treatments.Copyright © 2020 Elsevier Ltd and ISBI. All rights reserved.

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