Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds
<p>Three-dimensional collagen/chitosan scaffolds fabricated by freeze-drying technique in 96-well polystyrene and PDMS plates were optimized during this study. Surface tension is, by and large, one of the most limiting factors in fabricating freeze-dried scaffolds in small format well plates....
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格式: | Thesis |
語言: | English |
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2014
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author | Xue, B Bin Xue |
author2 | Cui, Z |
author_facet | Cui, Z Xue, B Bin Xue |
author_sort | Xue, B |
collection | OXFORD |
description | <p>Three-dimensional collagen/chitosan scaffolds fabricated by freeze-drying technique in 96-well polystyrene and PDMS plates were optimized during this study. Surface tension is, by and large, one of the most limiting factors in fabricating freeze-dried scaffolds in small format well plates. Traditionally, bowl-shaped top surfaces of collagen/chitosan scaffolds were common in polystyrene 96-well plate; whereas for PDMS 96-well plate, dome-shaped surfaces were formed. These surface tension phenomena are not desirable in cell studies especially during initial cell seeding. A combination of surface treatment and change of freeze-drying regime were developed to mitigate the surface tension problem in PS and PDMS 96-well plates respectively. Collagen/chitosan scaffolds of varying concentration and composition were experimented in both polystyrene and PDMS 96-well plates. Thin water film treatment with UV cross-linking was successfully used to eliminate meniscus in PS well plates; pre-cooling, on the other hand, was utilised to treat scaffold solutions in PDMS well plates. The resultant matrices all had flat top surfaces and average thickness of 1 mm. As expected, scaffolds with lower overall polymer concentration or, from a compositional perspective, scaffolds with high chitosan content generally had larger pores. Microscopic observation by multi-photon microscope was performed and chemical analyses were conducted to characterize the surface-treated scaffolds. In addition, scaffolds were tested <em>in vitro</em> using DLD-1 cells, hMSCs and fibroblasts for their biological performance. The purpose of this study was to address the problem of using small format culture wells for the fabrication of freeze-dried collagen-based scaffolds for studies of cell growth in 3D culture and in microfluidic perfusion bioreactors.</p> |
first_indexed | 2024-03-07T05:51:30Z |
format | Thesis |
id | oxford-uuid:e90a8ec1-1f1b-4427-858d-0b8f16e62be0 |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T05:51:30Z |
publishDate | 2014 |
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spelling | oxford-uuid:e90a8ec1-1f1b-4427-858d-0b8f16e62be02022-03-27T10:51:20ZDevelopment and optimisation of three-dimensional freeze-dried collagen-based scaffoldsThesishttp://purl.org/coar/resource_type/c_bdccuuid:e90a8ec1-1f1b-4427-858d-0b8f16e62be0Biomedical engineeringEnglishOxford University Research Archive - Valet2014Xue, BBin XueCui, Z<p>Three-dimensional collagen/chitosan scaffolds fabricated by freeze-drying technique in 96-well polystyrene and PDMS plates were optimized during this study. Surface tension is, by and large, one of the most limiting factors in fabricating freeze-dried scaffolds in small format well plates. Traditionally, bowl-shaped top surfaces of collagen/chitosan scaffolds were common in polystyrene 96-well plate; whereas for PDMS 96-well plate, dome-shaped surfaces were formed. These surface tension phenomena are not desirable in cell studies especially during initial cell seeding. A combination of surface treatment and change of freeze-drying regime were developed to mitigate the surface tension problem in PS and PDMS 96-well plates respectively. Collagen/chitosan scaffolds of varying concentration and composition were experimented in both polystyrene and PDMS 96-well plates. Thin water film treatment with UV cross-linking was successfully used to eliminate meniscus in PS well plates; pre-cooling, on the other hand, was utilised to treat scaffold solutions in PDMS well plates. The resultant matrices all had flat top surfaces and average thickness of 1 mm. As expected, scaffolds with lower overall polymer concentration or, from a compositional perspective, scaffolds with high chitosan content generally had larger pores. Microscopic observation by multi-photon microscope was performed and chemical analyses were conducted to characterize the surface-treated scaffolds. In addition, scaffolds were tested <em>in vitro</em> using DLD-1 cells, hMSCs and fibroblasts for their biological performance. The purpose of this study was to address the problem of using small format culture wells for the fabrication of freeze-dried collagen-based scaffolds for studies of cell growth in 3D culture and in microfluidic perfusion bioreactors.</p> |
spellingShingle | Biomedical engineering Xue, B Bin Xue Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title | Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title_full | Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title_fullStr | Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title_full_unstemmed | Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title_short | Development and optimisation of three-dimensional freeze-dried collagen-based scaffolds |
title_sort | development and optimisation of three dimensional freeze dried collagen based scaffolds |
topic | Biomedical engineering |
work_keys_str_mv | AT xueb developmentandoptimisationofthreedimensionalfreezedriedcollagenbasedscaffolds AT binxue developmentandoptimisationofthreedimensionalfreezedriedcollagenbasedscaffolds |