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Bioglass/carbonate apatite/collagen composite scaffold dissolution products promote human osteoblast differentiation
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Bioglass-carbonate apatite-collagen composite scaffold dissolution products promote human osteoblast differentiation.pdf | Accepted version | 1.6 MB | Adobe PDF | View/Open |
Title: | Bioglass/carbonate apatite/collagen composite scaffold dissolution products promote human osteoblast differentiation |
Authors: | Ferreira, SA Young, G Jones, JR Rankin, S |
Item Type: | Journal Article |
Abstract: | OssiMend® Bioactive (Collagen Matrix Inc., NJ) is a three-component porous composite bone graft device of 45S5 Bioglass/carbonate apatite/collagen. Our in vitro studies showed that conditioned media of the dissolution products of OssiMend Bioactive stimulated primary human osteoblasts to form mineralized bone-like nodules in vitro in one week, in basal culture media (no osteogenic supplements). Osteoblast differentiation was followed by gene expression analysis and a mineralization assay. In contrast, the dissolution products from commercial OssiMend (Bioglass-free carbonate apatite/collagen scaffolds), or from 45S5 Bioglass particulate alone, did not induce the mineralization of the extracellular matrix, but did induce osteoblast differentiation to mature osteoblasts, evidenced by the strong upregulation of BGLAP and IBSP mRNA levels. The calcium ions and soluble silicon species released from 45S5 Bioglass particles and additional phosphorus release from OssiMend mediated the osteostimulatory effects. Medium conditioned with OssiMend Bioactive dissolution had a much higher concentration of phosphorus and silicon than media conditioned with OssiMend and 45S5 Bioglass alone. While OssiMend and OssiMend Bioactive led to calcium precipitation in cell culture media, OssiMend Bioactive produced a higher concentration of soluble silicon than 45S5 Bioglass and higher dissolution of phosphorus than OssiMend. These in vitro results suggest that adding 45S5 Bioglass to OssiMend produces a synergistic osteostimulation effect on primary human osteoblasts. |
Issue Date: | Jan-2021 |
Date of Acceptance: | 12-Aug-2020 |
URI: | http://hdl.handle.net/10044/1/82444 |
DOI: | 10.1016/j.msec.2020.111393 |
ISSN: | 0928-4931 |
Publisher: | Elsevier BV |
Start Page: | 1 |
End Page: | 13 |
Journal / Book Title: | Materials Science and Engineering: C |
Volume: | 118 |
Copyright Statement: | © 2020 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/ |
Keywords: | 0903 Biomedical Engineering 0912 Materials Engineering Biomedical Engineering |
Publication Status: | Published online |
Article Number: | 111393 |
Online Publication Date: | 2020-08-22 |
Appears in Collections: | Materials National Heart and Lung Institute Faculty of Medicine Faculty of Natural Sciences |
This item is licensed under a Creative Commons License