Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering

Abstract We aimed to construct a biodegradable transparent scaffold for culturing corneal endothelial cells by incorporating chitosan nanoparticles (CSNPs) into chitosan/polycaprolactone (PCL) membranes. Various ratios of CSNP/PCL were prepared in the presence of constant concentration of chitosan a...

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Main Authors: Tahereh Tayebi, Alireza Baradaran-Rafii, Abbas Hajifathali, Azam Rahimpour, Hakimeh Zali, Alireza Shaabani, Hassan Niknejad
Format: Article
Language:English
Published: Nature Portfolio 2021-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-86340-w
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author Tahereh Tayebi
Alireza Baradaran-Rafii
Abbas Hajifathali
Azam Rahimpour
Hakimeh Zali
Alireza Shaabani
Hassan Niknejad
author_facet Tahereh Tayebi
Alireza Baradaran-Rafii
Abbas Hajifathali
Azam Rahimpour
Hakimeh Zali
Alireza Shaabani
Hassan Niknejad
author_sort Tahereh Tayebi
collection DOAJ
description Abstract We aimed to construct a biodegradable transparent scaffold for culturing corneal endothelial cells by incorporating chitosan nanoparticles (CSNPs) into chitosan/polycaprolactone (PCL) membranes. Various ratios of CSNP/PCL were prepared in the presence of constant concentration of chitosan and the films were constructed by solvent casting method. Scaffold properties including transparency, surface wettability, FTIR, and biocompatibility were examined. SEM imaging, H&E staining, and cell count were performed to investigate the HCECs adhesion. The phenotypic maintenance of the cells during culture was investigated by flow cytometry. Transparency and surface wettability improved by increasing the CSNP/PCL ratio. The CSNP/PCL 50/25, which has the lowest WCA, showed comparable transparency with human acellular corneal stroma. The scaffold was not cytotoxic and promoted the HCECs proliferation as evaluated by MTT assay. Cell counting, flow cytometry, SEM, and H&E results showed appropriate attachment of HCECs to the scaffold which formed a compact monolayer. The developed scaffold seems to be suitable for use in corneal endothelial regeneration in terms of transparency and biocompatibility.
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spelling doaj.art-9a5fdf840f354daaa3bdfb742c0716432022-12-21T22:55:08ZengNature PortfolioScientific Reports2045-23222021-03-0111111210.1038/s41598-021-86340-wBiofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineeringTahereh Tayebi0Alireza Baradaran-Rafii1Abbas Hajifathali2Azam Rahimpour3Hakimeh Zali4Alireza Shaabani5Hassan Niknejad6Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical SciencesOphthalmic Research Center, Department of Ophthalmology, Shahid Labbafinejad Medical Center, Shahid Beheshti University of Medical SciencesHematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical SciencesDepartment of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical SciencesDepartment of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical SciencesDepartment of Polymer and Materials Chemistry, Faculty of Chemistry and Petroleum Science, Shahid Beheshti UniversityDepartment of Pharmacology, School of Medicine, Shahid Beheshti University of Medical SciencesAbstract We aimed to construct a biodegradable transparent scaffold for culturing corneal endothelial cells by incorporating chitosan nanoparticles (CSNPs) into chitosan/polycaprolactone (PCL) membranes. Various ratios of CSNP/PCL were prepared in the presence of constant concentration of chitosan and the films were constructed by solvent casting method. Scaffold properties including transparency, surface wettability, FTIR, and biocompatibility were examined. SEM imaging, H&E staining, and cell count were performed to investigate the HCECs adhesion. The phenotypic maintenance of the cells during culture was investigated by flow cytometry. Transparency and surface wettability improved by increasing the CSNP/PCL ratio. The CSNP/PCL 50/25, which has the lowest WCA, showed comparable transparency with human acellular corneal stroma. The scaffold was not cytotoxic and promoted the HCECs proliferation as evaluated by MTT assay. Cell counting, flow cytometry, SEM, and H&E results showed appropriate attachment of HCECs to the scaffold which formed a compact monolayer. The developed scaffold seems to be suitable for use in corneal endothelial regeneration in terms of transparency and biocompatibility.https://doi.org/10.1038/s41598-021-86340-w
spellingShingle Tahereh Tayebi
Alireza Baradaran-Rafii
Abbas Hajifathali
Azam Rahimpour
Hakimeh Zali
Alireza Shaabani
Hassan Niknejad
Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
Scientific Reports
title Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
title_full Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
title_fullStr Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
title_full_unstemmed Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
title_short Biofabrication of chitosan/chitosan nanoparticles/polycaprolactone transparent membrane for corneal endothelial tissue engineering
title_sort biofabrication of chitosan chitosan nanoparticles polycaprolactone transparent membrane for corneal endothelial tissue engineering
url https://doi.org/10.1038/s41598-021-86340-w
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