Fabrication and characterization of magnetic scaffolds in bone tissue engineering

Magnetic scaffolds gained much popularity for tissue repair in the recent years. Here we focus on magnetic nanocomposite scaffolds made of poly-(caprolactone) (PCL), tri- calcium phosphate (TCP) and Iron Oxide magnetic nanoparticles (MNPs) for bone repair. The chemical, thermal, and mechanical prope...

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Main Author: Chia, Amanda
Other Authors: Padmalosini Muthukumaran
Format: Final Year Project
Language:English
Published: 2018
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Online Access:http://hdl.handle.net/10356/75815
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-758152023-03-03T15:40:13Z Fabrication and characterization of magnetic scaffolds in bone tissue engineering Chia, Amanda Padmalosini Muthukumaran Teoh Swee Hin School of Chemical and Biomedical Engineering DRNTU::Engineering::Bioengineering Magnetic scaffolds gained much popularity for tissue repair in the recent years. Here we focus on magnetic nanocomposite scaffolds made of poly-(caprolactone) (PCL), tri- calcium phosphate (TCP) and Iron Oxide magnetic nanoparticles (MNPs) for bone repair. The chemical, thermal, and mechanical properties of the scaffolds and the in vitro cell responses were examined comprehensively to investigate their effectiveness for use as bone scaffolds. The scaffolds were fabricated with a solvent free and efficient method known as cryomilling, resulting in homogeneous distribution of MNPs and TCP in PCL matrix. Chemical properties of PCL, TCP and MNP were all retained in the composite. Thermal properties of the scaffold were not significantly different from pure PCL, an FDA approved biomaterial. The mechanical stiffness increased significantly with the addition of TCP and MNPs, but lies within the Young Modulus range of cortical bone. For in vitro studies, pre-osteoblast cells (MC3T3-E1) were used. The cell proliferation of magnetic scaffolds (5%MNPs) with the exposure to PEMF had a 25.5% higher proliferation than the same scaffold composition with no exposure to PEMF. Cell differentiation at 2.5%MNP was significantly higher than PCL/TCP scaffold with PEMF exposed, revealing the osteogenic property of MNPs. Even at day 28, both 2.5%MNP and 5%MNP scaffolds have a significantly higher cell differentiation with PEMF exposed. Cell mineralization, as assessed by the quantification of calcium deposits, was significantly enhanced particularly on 1%MNP scaffolds. FESEM images of cell interaction suggests that PEMF provided a microenvironment suitable for differentiation as cell morphology resembles that of osteocytes. The results are indicative of the excellent physical properties and biocompatibility of PCL-TCP-MNP scaffolds as well as PEMF-induced enhanced bone healing, suggesting potential use of the magnetic scaffolds and PEMF for bone repair and regeneration. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2018-06-18T06:22:13Z 2018-06-18T06:22:13Z 2018 Final Year Project (FYP) http://hdl.handle.net/10356/75815 en Nanyang Technological University 69 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Bioengineering
spellingShingle DRNTU::Engineering::Bioengineering
Chia, Amanda
Fabrication and characterization of magnetic scaffolds in bone tissue engineering
description Magnetic scaffolds gained much popularity for tissue repair in the recent years. Here we focus on magnetic nanocomposite scaffolds made of poly-(caprolactone) (PCL), tri- calcium phosphate (TCP) and Iron Oxide magnetic nanoparticles (MNPs) for bone repair. The chemical, thermal, and mechanical properties of the scaffolds and the in vitro cell responses were examined comprehensively to investigate their effectiveness for use as bone scaffolds. The scaffolds were fabricated with a solvent free and efficient method known as cryomilling, resulting in homogeneous distribution of MNPs and TCP in PCL matrix. Chemical properties of PCL, TCP and MNP were all retained in the composite. Thermal properties of the scaffold were not significantly different from pure PCL, an FDA approved biomaterial. The mechanical stiffness increased significantly with the addition of TCP and MNPs, but lies within the Young Modulus range of cortical bone. For in vitro studies, pre-osteoblast cells (MC3T3-E1) were used. The cell proliferation of magnetic scaffolds (5%MNPs) with the exposure to PEMF had a 25.5% higher proliferation than the same scaffold composition with no exposure to PEMF. Cell differentiation at 2.5%MNP was significantly higher than PCL/TCP scaffold with PEMF exposed, revealing the osteogenic property of MNPs. Even at day 28, both 2.5%MNP and 5%MNP scaffolds have a significantly higher cell differentiation with PEMF exposed. Cell mineralization, as assessed by the quantification of calcium deposits, was significantly enhanced particularly on 1%MNP scaffolds. FESEM images of cell interaction suggests that PEMF provided a microenvironment suitable for differentiation as cell morphology resembles that of osteocytes. The results are indicative of the excellent physical properties and biocompatibility of PCL-TCP-MNP scaffolds as well as PEMF-induced enhanced bone healing, suggesting potential use of the magnetic scaffolds and PEMF for bone repair and regeneration.
author2 Padmalosini Muthukumaran
author_facet Padmalosini Muthukumaran
Chia, Amanda
format Final Year Project
author Chia, Amanda
author_sort Chia, Amanda
title Fabrication and characterization of magnetic scaffolds in bone tissue engineering
title_short Fabrication and characterization of magnetic scaffolds in bone tissue engineering
title_full Fabrication and characterization of magnetic scaffolds in bone tissue engineering
title_fullStr Fabrication and characterization of magnetic scaffolds in bone tissue engineering
title_full_unstemmed Fabrication and characterization of magnetic scaffolds in bone tissue engineering
title_sort fabrication and characterization of magnetic scaffolds in bone tissue engineering
publishDate 2018
url http://hdl.handle.net/10356/75815
_version_ 1759857709519208448