Sustained Release of BMP-2 in Bioprinted Alginate for Osteogenicity in Mice and Rats
The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the s...
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Published in | PloS one Vol. 8; no. 8; p. e72610 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
19.08.2013
Public Library of Science (PLoS) |
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Abstract | The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo. |
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AbstractList | The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo. The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo . The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo.The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo. |
Audience | Academic |
Author | Weinans, Harrie Dhert, Wouter J. A. Alblas, Jacqueline van der Stok, Johan Öner, F. Cumhur Leeuwenburgh, Sander C. G. Wang, Huanan Poldervaart, Michelle T. |
AuthorAffiliation | 4 Department of Biomechanical Engineering, Delft University of Technology, Delft, The Netherlands 5 Department of Rheumatology, University Medical Center Utrecht, Utrecht, The Netherlands 6 Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands 1 Department of Orthopaedics, University Medical Center Utrecht, Utrecht, The Netherlands National University of Ireland, Galway, Ireland 3 Department of Orthopaedics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands 2 Department of Biomaterials, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands |
AuthorAffiliation_xml | – name: 1 Department of Orthopaedics, University Medical Center Utrecht, Utrecht, The Netherlands – name: 5 Department of Rheumatology, University Medical Center Utrecht, Utrecht, The Netherlands – name: 4 Department of Biomechanical Engineering, Delft University of Technology, Delft, The Netherlands – name: 3 Department of Orthopaedics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands – name: 2 Department of Biomaterials, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands – name: National University of Ireland, Galway, Ireland – name: 6 Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands |
Author_xml | – sequence: 1 givenname: Michelle T. surname: Poldervaart fullname: Poldervaart, Michelle T. – sequence: 2 givenname: Huanan surname: Wang fullname: Wang, Huanan – sequence: 3 givenname: Johan surname: van der Stok fullname: van der Stok, Johan – sequence: 4 givenname: Harrie surname: Weinans fullname: Weinans, Harrie – sequence: 5 givenname: Sander C. G. surname: Leeuwenburgh fullname: Leeuwenburgh, Sander C. G. – sequence: 6 givenname: F. Cumhur surname: Öner fullname: Öner, F. Cumhur – sequence: 7 givenname: Wouter J. A. surname: Dhert fullname: Dhert, Wouter J. A. – sequence: 8 givenname: Jacqueline surname: Alblas fullname: Alblas, Jacqueline |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23977328$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2013 Public Library of Science 2013 Poldervaart et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2013 Poldervaart et al 2013 Poldervaart et al |
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DocumentTitleAlternate | Prolonged BMP-2 Release in Bioprinted Scaffolds |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: MP SL H. Weinans FCO WD JA. Performed the experiments: MP H. Wang JvdS. Analyzed the data: MP H. Wang JvdS WD JA. Contributed reagents/materials/analysis tools: H. Wang SL H. Weinans. Wrote the paper: MP H. Wang JvdS H. Weinans SL FCO WD JA. |
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SubjectTerms | 3D printing Alginates - pharmacology Alginic acid Animals Biocompatibility Biodegradation Biological activity Biological properties Biology Biomechanics Biomedical materials Bioprinting - methods Bone growth Bone morphogenetic protein 2 Bone Morphogenetic Protein 2 - metabolism Bone morphogenetic proteins Calcium Calcium phosphate Calcium phosphates Cell Differentiation - drug effects Comparative analysis Controlled release Delayed-Action Preparations Differentiation Drug dosages Engineering Female Fractures Gelatin Gelatin - pharmacology Glucuronic Acid - pharmacology Goats Growth factors Hexuronic Acids - pharmacology Humans Hydrogels Hydroxyapatites - pharmacology Implantation Kinetics Materials Science Medicine Mice, Nude Microparticles Microspheres Multipotent Stem Cells - cytology Multipotent Stem Cells - drug effects Multipotent Stem Cells - metabolism Osteocalcin - metabolism Osteogenesis Osteogenesis - drug effects Phosphates Polymers Printing Product introduction Proteins Rats Rats, Wistar Scaffolds Stromal cells Stromal Cells - cytology Stromal Cells - drug effects Stromal Cells - metabolism Subcutaneous Tissue - metabolism Surgical implants Sustained release Three dimensional printing Tissue engineering Tissue Scaffolds - chemistry Vehicles |
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Title | Sustained Release of BMP-2 in Bioprinted Alginate for Osteogenicity in Mice and Rats |
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