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Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing
The early and effective treatment of wounds is vital to ensure proper wound closure and healing with appropriate functional and cosmetic outcomes. The use of human amnion membranes for wound care has been shown to be safe and effective. However, the difficulty in handling and placing thin sheets of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430059/ https://www.ncbi.nlm.nih.gov/pubmed/28941321 http://dx.doi.org/10.1002/sctm.17-0053 |
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author | Murphy, Sean V. Skardal, Aleksander Song, Lujie Sutton, Khiry Haug, Rebecca Mack, David L. Jackson, John Soker, Shay Atala, Anthony |
author_facet | Murphy, Sean V. Skardal, Aleksander Song, Lujie Sutton, Khiry Haug, Rebecca Mack, David L. Jackson, John Soker, Shay Atala, Anthony |
author_sort | Murphy, Sean V. |
collection | PubMed |
description | The early and effective treatment of wounds is vital to ensure proper wound closure and healing with appropriate functional and cosmetic outcomes. The use of human amnion membranes for wound care has been shown to be safe and effective. However, the difficulty in handling and placing thin sheets of membrane, and the high costs associated with the use of living cellularized tissue has limited the clinical application of amniotic membrane wound healing products. Here, we describe a novel amnion membrane‐derived product, processed to result in a cell‐free solution, while maintaining high concentrations of cell‐derived cytokines and growth factors. The solubilized amnion membrane (SAM) combined with the carrier hyaluronic acid (HA) hydrogel (HA‐SAM) is easy to produce, store, and apply to wounds. We demonstrated the efficacy of HA‐SAM as a wound treatment using a full‐thickness murine wound model. HA‐SAM significantly accelerated wound closure through re‐epithelialization and prevented wound contraction. HA‐SAM‐treated wounds had thicker regenerated skin, increased total number of blood vessels, and greater numbers of proliferating keratinocytes within the epidermis. Overall, this study confirms the efficacy of the amnion membrane as a wound treatment/dressing, and overcomes many of the limitations associated with using fresh, cryopreserved, or dehydrated tissue by providing a hydrogel delivery system for SAM. Stem Cells Translational Medicine 2017;6:2020–2032 |
format | Online Article Text |
id | pubmed-6430059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64300592019-04-04 Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing Murphy, Sean V. Skardal, Aleksander Song, Lujie Sutton, Khiry Haug, Rebecca Mack, David L. Jackson, John Soker, Shay Atala, Anthony Stem Cells Transl Med Translational Research Articles and Reviews The early and effective treatment of wounds is vital to ensure proper wound closure and healing with appropriate functional and cosmetic outcomes. The use of human amnion membranes for wound care has been shown to be safe and effective. However, the difficulty in handling and placing thin sheets of membrane, and the high costs associated with the use of living cellularized tissue has limited the clinical application of amniotic membrane wound healing products. Here, we describe a novel amnion membrane‐derived product, processed to result in a cell‐free solution, while maintaining high concentrations of cell‐derived cytokines and growth factors. The solubilized amnion membrane (SAM) combined with the carrier hyaluronic acid (HA) hydrogel (HA‐SAM) is easy to produce, store, and apply to wounds. We demonstrated the efficacy of HA‐SAM as a wound treatment using a full‐thickness murine wound model. HA‐SAM significantly accelerated wound closure through re‐epithelialization and prevented wound contraction. HA‐SAM‐treated wounds had thicker regenerated skin, increased total number of blood vessels, and greater numbers of proliferating keratinocytes within the epidermis. Overall, this study confirms the efficacy of the amnion membrane as a wound treatment/dressing, and overcomes many of the limitations associated with using fresh, cryopreserved, or dehydrated tissue by providing a hydrogel delivery system for SAM. Stem Cells Translational Medicine 2017;6:2020–2032 John Wiley and Sons Inc. 2017-09-23 /pmc/articles/PMC6430059/ /pubmed/28941321 http://dx.doi.org/10.1002/sctm.17-0053 Text en © 2017 The Authors stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Translational Research Articles and Reviews Murphy, Sean V. Skardal, Aleksander Song, Lujie Sutton, Khiry Haug, Rebecca Mack, David L. Jackson, John Soker, Shay Atala, Anthony Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title | Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title_full | Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title_fullStr | Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title_full_unstemmed | Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title_short | Solubilized Amnion Membrane Hyaluronic Acid Hydrogel Accelerates Full‐Thickness Wound Healing |
title_sort | solubilized amnion membrane hyaluronic acid hydrogel accelerates full‐thickness wound healing |
topic | Translational Research Articles and Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430059/ https://www.ncbi.nlm.nih.gov/pubmed/28941321 http://dx.doi.org/10.1002/sctm.17-0053 |
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