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In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation

This study compared the effects of implanting two interpenetrating polymer networks (IPNs) into rabbit corneas. The first (Implant 1) was based on PEG-diacrylate, the second (Implant 2) was based on PEG-diacrylamide. There were inserted into deep stromal pockets created using a manual surgical techn...

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Autores principales: Tan, Xiao Wei, Hartman, Laura, Tan, Kim Peng, Poh, Rebekah, Myung, David, Zheng, Luo Luo, Waters, Dale, Noolandi, Jaan, Beuerman, Roger W., Frank, Curtis W., Ta, Christopher N., Tan, Donald TH, Mehta, Jodhbir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3620449/
https://www.ncbi.nlm.nih.gov/pubmed/23354737
http://dx.doi.org/10.1007/s10856-012-4848-3
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author Tan, Xiao Wei
Hartman, Laura
Tan, Kim Peng
Poh, Rebekah
Myung, David
Zheng, Luo Luo
Waters, Dale
Noolandi, Jaan
Beuerman, Roger W.
Frank, Curtis W.
Ta, Christopher N.
Tan, Donald TH
Mehta, Jodhbir S.
author_facet Tan, Xiao Wei
Hartman, Laura
Tan, Kim Peng
Poh, Rebekah
Myung, David
Zheng, Luo Luo
Waters, Dale
Noolandi, Jaan
Beuerman, Roger W.
Frank, Curtis W.
Ta, Christopher N.
Tan, Donald TH
Mehta, Jodhbir S.
author_sort Tan, Xiao Wei
collection PubMed
description This study compared the effects of implanting two interpenetrating polymer networks (IPNs) into rabbit corneas. The first (Implant 1) was based on PEG-diacrylate, the second (Implant 2) was based on PEG-diacrylamide. There were inserted into deep stromal pockets created using a manual surgical technique for either 3 or 6 months. The implanted corneas were compared with normal and sham-operated corneas through slit lamp observation, anterior segment optical coherence tomography, in vivo confocal scanning and histological examination. Corneas with Implant 1 (based on PEG-diacrylate) developed diffuse haze, ulcers and opacities within 3 months, while corneas with Implant 2 (based on PEG-diacrylamide) remained clear at 6 months. They also exhibited normal numbers of epithelial cell layers, without any immune cell infiltration, inflammation, oedema or neovascularisation at post-operative 6 month. Morphological studies showed transient epithelial layer thinning over the hydrogel inserted area and elevated keratocyte activity at 3 months; however, the epithelium thickness and keratocyte morphology were improved at 6 months. Implant 2 exhibited superior in vivo biocompatibility and higher optical clarity than Implant 1. PEG-diacrylamide-based IPN hydrogel is therefore a potential candidate for corneal inlays to correct refractive error.
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spelling pubmed-36204492013-04-10 In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation Tan, Xiao Wei Hartman, Laura Tan, Kim Peng Poh, Rebekah Myung, David Zheng, Luo Luo Waters, Dale Noolandi, Jaan Beuerman, Roger W. Frank, Curtis W. Ta, Christopher N. Tan, Donald TH Mehta, Jodhbir S. J Mater Sci Mater Med Article This study compared the effects of implanting two interpenetrating polymer networks (IPNs) into rabbit corneas. The first (Implant 1) was based on PEG-diacrylate, the second (Implant 2) was based on PEG-diacrylamide. There were inserted into deep stromal pockets created using a manual surgical technique for either 3 or 6 months. The implanted corneas were compared with normal and sham-operated corneas through slit lamp observation, anterior segment optical coherence tomography, in vivo confocal scanning and histological examination. Corneas with Implant 1 (based on PEG-diacrylate) developed diffuse haze, ulcers and opacities within 3 months, while corneas with Implant 2 (based on PEG-diacrylamide) remained clear at 6 months. They also exhibited normal numbers of epithelial cell layers, without any immune cell infiltration, inflammation, oedema or neovascularisation at post-operative 6 month. Morphological studies showed transient epithelial layer thinning over the hydrogel inserted area and elevated keratocyte activity at 3 months; however, the epithelium thickness and keratocyte morphology were improved at 6 months. Implant 2 exhibited superior in vivo biocompatibility and higher optical clarity than Implant 1. PEG-diacrylamide-based IPN hydrogel is therefore a potential candidate for corneal inlays to correct refractive error. Springer US 2013-01-26 2013 /pmc/articles/PMC3620449/ /pubmed/23354737 http://dx.doi.org/10.1007/s10856-012-4848-3 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Tan, Xiao Wei
Hartman, Laura
Tan, Kim Peng
Poh, Rebekah
Myung, David
Zheng, Luo Luo
Waters, Dale
Noolandi, Jaan
Beuerman, Roger W.
Frank, Curtis W.
Ta, Christopher N.
Tan, Donald TH
Mehta, Jodhbir S.
In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title_full In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title_fullStr In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title_full_unstemmed In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title_short In vivo biocompatibility of two PEG/PAA interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
title_sort in vivo biocompatibility of two peg/paa interpenetrating polymer networks as corneal inlays following deep stromal pocket implantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3620449/
https://www.ncbi.nlm.nih.gov/pubmed/23354737
http://dx.doi.org/10.1007/s10856-012-4848-3
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