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Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane

Human derived composite amnion-chorion membrane (ACM) has been used to facilitate wound healing due to reported anti-inflammatory properties and promotion of cell proliferation. This study aimed to assess the antimicrobial properties of the ACM using novel methods to visualize the antimicrobial effi...

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Autores principales: Palanker, Nathan D., Lee, Chun-Teh, Weltman, Robin L., Tribble, Gena D., van der Hoeven, Ransome, Hong, Jianming, Wang, Bingyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821917/
https://www.ncbi.nlm.nih.gov/pubmed/31666625
http://dx.doi.org/10.1038/s41598-019-52150-4
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author Palanker, Nathan D.
Lee, Chun-Teh
Weltman, Robin L.
Tribble, Gena D.
van der Hoeven, Ransome
Hong, Jianming
Wang, Bingyan
author_facet Palanker, Nathan D.
Lee, Chun-Teh
Weltman, Robin L.
Tribble, Gena D.
van der Hoeven, Ransome
Hong, Jianming
Wang, Bingyan
author_sort Palanker, Nathan D.
collection PubMed
description Human derived composite amnion-chorion membrane (ACM) has been used to facilitate wound healing due to reported anti-inflammatory properties and promotion of cell proliferation. This study aimed to assess the antimicrobial properties of the ACM using novel methods to visualize the antimicrobial efficacy of membranes in situ at different time points. Porcine Pericardium Collagen Membranes (PPCM) served as membrane controls. Circular pieces of the membranes were used in three different assays: insert, agar contact and glass-bottom well assays. Streptococcus gordonii were spotted onto the membranes and the plates were subsequently centrifuged to ensure direct bacterial contact with the membranes in the insert and agar contact assays, thus better mimicking bacterial adherence in the oral cavity. After incubation at 37 °C for 8, 24, and 48 hours, the membranes were dyed with the Live/Dead BacLight Bacterial Viability fluorescence stain and analyzed via confocal microscopy. The results demonstrated that the ACM completely inhibited bacterial growth at all time points, whereas the PPCM did not demonstrate any antimicrobial properties. Within the limits of this study, the ACM showed extremely high antimicrobial efficacy against oral streptococci. In addition, our methods may be useful in assessing antimicrobial properties for biomaterials with minimum diffusion ability, when traditional assessment methods are not applicable.
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spelling pubmed-68219172019-11-05 Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane Palanker, Nathan D. Lee, Chun-Teh Weltman, Robin L. Tribble, Gena D. van der Hoeven, Ransome Hong, Jianming Wang, Bingyan Sci Rep Article Human derived composite amnion-chorion membrane (ACM) has been used to facilitate wound healing due to reported anti-inflammatory properties and promotion of cell proliferation. This study aimed to assess the antimicrobial properties of the ACM using novel methods to visualize the antimicrobial efficacy of membranes in situ at different time points. Porcine Pericardium Collagen Membranes (PPCM) served as membrane controls. Circular pieces of the membranes were used in three different assays: insert, agar contact and glass-bottom well assays. Streptococcus gordonii were spotted onto the membranes and the plates were subsequently centrifuged to ensure direct bacterial contact with the membranes in the insert and agar contact assays, thus better mimicking bacterial adherence in the oral cavity. After incubation at 37 °C for 8, 24, and 48 hours, the membranes were dyed with the Live/Dead BacLight Bacterial Viability fluorescence stain and analyzed via confocal microscopy. The results demonstrated that the ACM completely inhibited bacterial growth at all time points, whereas the PPCM did not demonstrate any antimicrobial properties. Within the limits of this study, the ACM showed extremely high antimicrobial efficacy against oral streptococci. In addition, our methods may be useful in assessing antimicrobial properties for biomaterials with minimum diffusion ability, when traditional assessment methods are not applicable. Nature Publishing Group UK 2019-10-30 /pmc/articles/PMC6821917/ /pubmed/31666625 http://dx.doi.org/10.1038/s41598-019-52150-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Palanker, Nathan D.
Lee, Chun-Teh
Weltman, Robin L.
Tribble, Gena D.
van der Hoeven, Ransome
Hong, Jianming
Wang, Bingyan
Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title_full Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title_fullStr Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title_full_unstemmed Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title_short Antimicrobial Efficacy Assessment of Human Derived Composite Amnion-Chorion Membrane
title_sort antimicrobial efficacy assessment of human derived composite amnion-chorion membrane
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821917/
https://www.ncbi.nlm.nih.gov/pubmed/31666625
http://dx.doi.org/10.1038/s41598-019-52150-4
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