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Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™

Skin plays an important role in defense against infection and other harmful biological agents. Due to its fragile structure, skin can be easily damaged by heat, chemicals, traumatic injuries and diseases. An autologous bilayered human skin equivalent, MyDerm™, was engineered to provide a living skin...

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Autores principales: Seet, Wan Tai, Maarof, Manira, Khairul Anuar, Khairoji, Chua, Kien-Hui, Ahmad Irfan, Abdul Wahab, Ng, Min Hwei, Saim Aminuddin, Bin, Idrus Ruszymah, Bt Hj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426510/
https://www.ncbi.nlm.nih.gov/pubmed/22927903
http://dx.doi.org/10.1371/journal.pone.0040978
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author Seet, Wan Tai
Maarof, Manira
Khairul Anuar, Khairoji
Chua, Kien-Hui
Ahmad Irfan, Abdul Wahab
Ng, Min Hwei
Saim Aminuddin, Bin
Idrus Ruszymah, Bt Hj
author_facet Seet, Wan Tai
Maarof, Manira
Khairul Anuar, Khairoji
Chua, Kien-Hui
Ahmad Irfan, Abdul Wahab
Ng, Min Hwei
Saim Aminuddin, Bin
Idrus Ruszymah, Bt Hj
author_sort Seet, Wan Tai
collection PubMed
description Skin plays an important role in defense against infection and other harmful biological agents. Due to its fragile structure, skin can be easily damaged by heat, chemicals, traumatic injuries and diseases. An autologous bilayered human skin equivalent, MyDerm™, was engineered to provide a living skin substitute to treat critical skin loss. However, one of the disadvantages of living skin substitute is its short shelf-life, hence limiting its distribution worldwide. The aim of this study was to evaluate the shelf-life of MyDerm™ through assessment of cell morphology, cell viability, population doubling time and functional gene expression levels before transplantation. Skin samples were digested with 0.6% Collagenase Type I followed by epithelial cells dissociation with TrypLE Select. Dermal fibroblasts and keratinocytes were culture-expanded to obtain sufficient cells for MyDerm™ construction. MyDerm™ was constructed with plasma-fibrin as temporary biomaterial and evaluated at 0, 24, 48 and 72 hours after storage at 4°C for its shelf-life determination. The morphology of skin cells derived from MyDerm™ remained unchanged across storage times. Cells harvested from MyDerm™ after storage appeared in good viability (90.5%±2.7% to 94.9%±1.6%) and had short population doubling time (58.4±8.7 to 76.9±19 hours). The modest drop in cell viability and increased in population doubling time at longer storage duration did not demonstrate a significant difference. Gene expression for CK10, CK14 and COL III were also comparable between different storage times. In conclusion, MyDerm™ can be stored in basal medium at 4°C for at least 72 hours before transplantation without compromising its functionality.
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spelling pubmed-34265102012-08-27 Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™ Seet, Wan Tai Maarof, Manira Khairul Anuar, Khairoji Chua, Kien-Hui Ahmad Irfan, Abdul Wahab Ng, Min Hwei Saim Aminuddin, Bin Idrus Ruszymah, Bt Hj PLoS One Research Article Skin plays an important role in defense against infection and other harmful biological agents. Due to its fragile structure, skin can be easily damaged by heat, chemicals, traumatic injuries and diseases. An autologous bilayered human skin equivalent, MyDerm™, was engineered to provide a living skin substitute to treat critical skin loss. However, one of the disadvantages of living skin substitute is its short shelf-life, hence limiting its distribution worldwide. The aim of this study was to evaluate the shelf-life of MyDerm™ through assessment of cell morphology, cell viability, population doubling time and functional gene expression levels before transplantation. Skin samples were digested with 0.6% Collagenase Type I followed by epithelial cells dissociation with TrypLE Select. Dermal fibroblasts and keratinocytes were culture-expanded to obtain sufficient cells for MyDerm™ construction. MyDerm™ was constructed with plasma-fibrin as temporary biomaterial and evaluated at 0, 24, 48 and 72 hours after storage at 4°C for its shelf-life determination. The morphology of skin cells derived from MyDerm™ remained unchanged across storage times. Cells harvested from MyDerm™ after storage appeared in good viability (90.5%±2.7% to 94.9%±1.6%) and had short population doubling time (58.4±8.7 to 76.9±19 hours). The modest drop in cell viability and increased in population doubling time at longer storage duration did not demonstrate a significant difference. Gene expression for CK10, CK14 and COL III were also comparable between different storage times. In conclusion, MyDerm™ can be stored in basal medium at 4°C for at least 72 hours before transplantation without compromising its functionality. Public Library of Science 2012-08-23 /pmc/articles/PMC3426510/ /pubmed/22927903 http://dx.doi.org/10.1371/journal.pone.0040978 Text en © 2012 Seet et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Seet, Wan Tai
Maarof, Manira
Khairul Anuar, Khairoji
Chua, Kien-Hui
Ahmad Irfan, Abdul Wahab
Ng, Min Hwei
Saim Aminuddin, Bin
Idrus Ruszymah, Bt Hj
Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title_full Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title_fullStr Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title_full_unstemmed Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title_short Shelf-Life Evaluation of Bilayered Human Skin Equivalent, MyDerm™
title_sort shelf-life evaluation of bilayered human skin equivalent, myderm™
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3426510/
https://www.ncbi.nlm.nih.gov/pubmed/22927903
http://dx.doi.org/10.1371/journal.pone.0040978
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