3D Plotted Biphasic Bone Scaffolds for Growth Factor Delivery: Biological Characterization In Vitro and In Vivo.
Alginates
/ chemistry
Animals
Bioprinting
/ methods
Bone and Bones
/ pathology
Calcium Phosphates
/ chemistry
Cell Differentiation
Cell Proliferation
Endothelial Cells
/ cytology
Hydrogels
/ chemistry
Male
Mesenchymal Stem Cells
/ cytology
Neovascularization, Physiologic
/ drug effects
Osteoblasts
/ cytology
Osteogenesis
Polysaccharides, Bacterial
/ chemistry
Rats
Rats, Wistar
Tissue Engineering
Tissue Scaffolds
/ chemistry
Vascular Endothelial Growth Factor A
/ chemistry
VEGF
bone formation
calcium phosphate cement
multichannel 3D plotting
osteogenic differentiation
vascularization
Journal
Advanced healthcare materials
ISSN: 2192-2659
Titre abrégé: Adv Healthc Mater
Pays: Germany
ID NLM: 101581613
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
23
11
2018
revised:
13
02
2019
pubmed:
7
3
2019
medline:
4
6
2020
entrez:
7
3
2019
Statut:
ppublish
Résumé
Bioprinting enables the integration of biological components into scaffolds during fabrication that has the advantage of high loading efficiency and better control of release and/or spatial positioning. In this study, a biphasic scaffold fabricated by extrusion-based 3D multichannel plotting of a calcium phosphate cement (CPC) paste and an alginate/gellan gum (AlgGG) hydrogel paste laden with the angiogenic factor VEGF (vascular endothelial growth factor) is investigated with regard to biological response in vitro and in vivo. Rat mesenchymal stromal cells are able to adhere and grow on both CPC and AlgGG strands, and differentiate toward osteoblasts. A sustained VEGF release is observed, which is able to stimulate endothelial cell proliferation as well as angiogenesis in vitro that indicates maintenance of its biological activity. After implantation into a segmental bone defect in the femur diaphysis of rats, a clear reduction of the defect size by newly formed bone tissue occurs from the distal and proximal ends of the host bone within 12 weeks. The CPC component shows excellent osteoconductivity whereas the local VEGF release from the AlgGG hydrogel gives rise to an enhanced vascularization of the defect region. This work contributes to the development of novel therapeutic concepts for improved bone regeneration which are based on 3D bioprinting.
Identifiants
pubmed: 30838778
doi: 10.1002/adhm.201801512
doi:
Substances chimiques
Alginates
0
Calcium Phosphates
0
Hydrogels
0
Polysaccharides, Bacterial
0
Vascular Endothelial Growth Factor A
0
gellan gum
7593U09I4D
calcium phosphate
97Z1WI3NDX
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1801512Subventions
Organisme : Saxon Ministry for Higher Education and Arts
ID : 4-7531.60/29/24
Pays : International
Organisme : German Federal and State Governments
Pays : International
Informations de copyright
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.