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Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier

BACKGROUND: Tissue engineering and bone substitutes are subjects of intensive ongoing research. If the healing of bone fractures is delayed, osteoinductive materials that induce mesenchymal stem cells (MSCs) to form bone are necessary. The use of Bone Morphogenetic Protein - 2 is a common means to e...

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Autores principales: Kissling, Steffen, Seidenstuecker, Michael, Pilz, Ingo H., Suedkamp, Norbert P., Mayr, Hermann O., Bernstein, Anke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874020/
https://www.ncbi.nlm.nih.gov/pubmed/27206764
http://dx.doi.org/10.1186/s12896-016-0275-8
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author Kissling, Steffen
Seidenstuecker, Michael
Pilz, Ingo H.
Suedkamp, Norbert P.
Mayr, Hermann O.
Bernstein, Anke
author_facet Kissling, Steffen
Seidenstuecker, Michael
Pilz, Ingo H.
Suedkamp, Norbert P.
Mayr, Hermann O.
Bernstein, Anke
author_sort Kissling, Steffen
collection PubMed
description BACKGROUND: Tissue engineering and bone substitutes are subjects of intensive ongoing research. If the healing of bone fractures is delayed, osteoinductive materials that induce mesenchymal stem cells (MSCs) to form bone are necessary. The use of Bone Morphogenetic Protein - 2 is a common means to enhance effectiveness and accelerate the healing process. A delivery system that maintains and releases BMP biological activity in controlled fashion at the surgical site while preventing systemic diffusion (and thereby the risk of undesirable effects by controlling the amount of protein implanted) is essential. In this study, we aimed to test a cylindrical TCP-scaffold (porosity ~ 40 %, mean pore size 5 μm, high interconnectivity) in comparison to BMP-2. Recombinant human BMP-2 was dissolved in different hydrogels as a carrier, namely gelatin and alginate cross-linked with CaCl(2)-solution, or a solution of GDL and CaCO(3). FITC-labeled Protein A was used as a model substance for rhBMP-2 in the pre-trials. For loading, the samples were put in a flow chamber and sealed with silicone rings. Using a directional vacuum, the samples were loaded with the alginate-BMP-2-mixture and the loading success monitored by observing changes in a fluorescent dye (FITC labeled Protein A) under a fluorescence microscope. A fluorescence reader and ELISA were employed to measure the release. Efficacy was determined in cell culture experiments (MG63 cells) via Live-Dead-Assay, FACS, WST-1-Assay, pNPP alkaline phosphatase assay and confocal microscopy. For statistical analysis, we calculated the mean and standard deviation and carried out an analysis of variance. RESULTS: Directional vacuum makes it possible to load nearly 100 % of the interconnected micropores with alginate mixed with rhBMP-2. Using alginate hardened with CaCl(2) as a carrier, BMP-2's release can be decelerated significantly longer than with other hydrogels - eg, for over 28 days. The effects on osteoblast-like cells were an increase of the growth rate and expression of alkaline phosphatase while triggering no toxic effect. CONCLUSION: The rhBMP-2-loaded microporous TCP scaffolds possess proliferative and osteoinductive potential. Alginate helps to lower the local growth factor dose below the cytotoxic limit, and allows the release period to be lengthened by at least 28 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-016-0275-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-48740202016-05-21 Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier Kissling, Steffen Seidenstuecker, Michael Pilz, Ingo H. Suedkamp, Norbert P. Mayr, Hermann O. Bernstein, Anke BMC Biotechnol Research Article BACKGROUND: Tissue engineering and bone substitutes are subjects of intensive ongoing research. If the healing of bone fractures is delayed, osteoinductive materials that induce mesenchymal stem cells (MSCs) to form bone are necessary. The use of Bone Morphogenetic Protein - 2 is a common means to enhance effectiveness and accelerate the healing process. A delivery system that maintains and releases BMP biological activity in controlled fashion at the surgical site while preventing systemic diffusion (and thereby the risk of undesirable effects by controlling the amount of protein implanted) is essential. In this study, we aimed to test a cylindrical TCP-scaffold (porosity ~ 40 %, mean pore size 5 μm, high interconnectivity) in comparison to BMP-2. Recombinant human BMP-2 was dissolved in different hydrogels as a carrier, namely gelatin and alginate cross-linked with CaCl(2)-solution, or a solution of GDL and CaCO(3). FITC-labeled Protein A was used as a model substance for rhBMP-2 in the pre-trials. For loading, the samples were put in a flow chamber and sealed with silicone rings. Using a directional vacuum, the samples were loaded with the alginate-BMP-2-mixture and the loading success monitored by observing changes in a fluorescent dye (FITC labeled Protein A) under a fluorescence microscope. A fluorescence reader and ELISA were employed to measure the release. Efficacy was determined in cell culture experiments (MG63 cells) via Live-Dead-Assay, FACS, WST-1-Assay, pNPP alkaline phosphatase assay and confocal microscopy. For statistical analysis, we calculated the mean and standard deviation and carried out an analysis of variance. RESULTS: Directional vacuum makes it possible to load nearly 100 % of the interconnected micropores with alginate mixed with rhBMP-2. Using alginate hardened with CaCl(2) as a carrier, BMP-2's release can be decelerated significantly longer than with other hydrogels - eg, for over 28 days. The effects on osteoblast-like cells were an increase of the growth rate and expression of alkaline phosphatase while triggering no toxic effect. CONCLUSION: The rhBMP-2-loaded microporous TCP scaffolds possess proliferative and osteoinductive potential. Alginate helps to lower the local growth factor dose below the cytotoxic limit, and allows the release period to be lengthened by at least 28 days. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-016-0275-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-20 /pmc/articles/PMC4874020/ /pubmed/27206764 http://dx.doi.org/10.1186/s12896-016-0275-8 Text en © Kissling et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kissling, Steffen
Seidenstuecker, Michael
Pilz, Ingo H.
Suedkamp, Norbert P.
Mayr, Hermann O.
Bernstein, Anke
Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title_full Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title_fullStr Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title_full_unstemmed Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title_short Sustained release of rhBMP-2 from microporous tricalciumphosphate using hydrogels as a carrier
title_sort sustained release of rhbmp-2 from microporous tricalciumphosphate using hydrogels as a carrier
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874020/
https://www.ncbi.nlm.nih.gov/pubmed/27206764
http://dx.doi.org/10.1186/s12896-016-0275-8
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