A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture

Background. Bone engineering requires thicker three-dimensional constructs than the maximum thickness supported by standard cell-culture techniques (2 mm). A flow-perfusion bioreactor was developed to provide chemotransportation to thick (6 mm) scaffolds. Methods. Polyurethane scaffolds, seeded wit...

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Main Authors: Alexander M. Sailon, Alexander C. Allori, Edward H. Davidson, Derek D. Reformat, Robert J. Allen, Stephen M. Warren
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/2009/873816
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spelling doaj-1d68453f9b464299a5947c83ab5d93b32020-11-24T21:31:44ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512009-01-01200910.1155/2009/873816873816A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell CultureAlexander M. Sailon0Alexander C. Allori1Edward H. Davidson2Derek D. Reformat3Robert J. Allen4Stephen M. Warren5The Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USAThe Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USAThe Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USAThe Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USAThe Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USAThe Institute of Reconstructive Plastic Surgery Laboratories, New York University Medical Center, New York, NY 10016, USABackground. Bone engineering requires thicker three-dimensional constructs than the maximum thickness supported by standard cell-culture techniques (2 mm). A flow-perfusion bioreactor was developed to provide chemotransportation to thick (6 mm) scaffolds. Methods. Polyurethane scaffolds, seeded with murine preosteoblasts, were loaded into a novel bioreactor. Control scaffolds remained in static culture. Samples were harvested at days 2, 4, 6, and 8 and analyzed for cellular distribution, viability, metabolic activity, and density at the periphery and core. Results. By day 8, static scaffolds had a periphery cell density of 67%±5.0%, while in the core it was 0.3%±0.3%. Flow-perfused scaffolds demonstrated peripheral cell density of 94%±8.3% and core density of 76%±3.1% at day 8. Conclusions. Flow perfusion provides chemotransportation to thick scaffolds. This system may permit high throughput study of 3D tissues in vitro and enable prefabrication of biological constructs large enough to solve clinical problems.http://dx.doi.org/10.1155/2009/873816
collection DOAJ
language English
format Article
sources DOAJ
author Alexander M. Sailon
Alexander C. Allori
Edward H. Davidson
Derek D. Reformat
Robert J. Allen
Stephen M. Warren
spellingShingle Alexander M. Sailon
Alexander C. Allori
Edward H. Davidson
Derek D. Reformat
Robert J. Allen
Stephen M. Warren
A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
Journal of Biomedicine and Biotechnology
author_facet Alexander M. Sailon
Alexander C. Allori
Edward H. Davidson
Derek D. Reformat
Robert J. Allen
Stephen M. Warren
author_sort Alexander M. Sailon
title A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
title_short A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
title_full A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
title_fullStr A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
title_full_unstemmed A Novel Flow-Perfusion Bioreactor Supports 3D Dynamic Cell Culture
title_sort novel flow-perfusion bioreactor supports 3d dynamic cell culture
publisher Hindawi Limited
series Journal of Biomedicine and Biotechnology
issn 1110-7243
1110-7251
publishDate 2009-01-01
description Background. Bone engineering requires thicker three-dimensional constructs than the maximum thickness supported by standard cell-culture techniques (2 mm). A flow-perfusion bioreactor was developed to provide chemotransportation to thick (6 mm) scaffolds. Methods. Polyurethane scaffolds, seeded with murine preosteoblasts, were loaded into a novel bioreactor. Control scaffolds remained in static culture. Samples were harvested at days 2, 4, 6, and 8 and analyzed for cellular distribution, viability, metabolic activity, and density at the periphery and core. Results. By day 8, static scaffolds had a periphery cell density of 67%±5.0%, while in the core it was 0.3%±0.3%. Flow-perfused scaffolds demonstrated peripheral cell density of 94%±8.3% and core density of 76%±3.1% at day 8. Conclusions. Flow perfusion provides chemotransportation to thick scaffolds. This system may permit high throughput study of 3D tissues in vitro and enable prefabrication of biological constructs large enough to solve clinical problems.
url http://dx.doi.org/10.1155/2009/873816
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