The Cocktail Effect of BMP-2 and TGF-β1 Loaded in Visible Light-Cured Glycol Chitosan Hydrogels for the Enhancement of Bone Formation in a Rat Tibial Defect Model.
Sun-Jung YoonYoungbum YooSang Eun NamHoon HyunDeok-Won LeeSewook UmSo Yeon KimSung Ok HongDae Hyeok YangHeung Jae ChunPublished in: Marine drugs (2018)
Bone tissue engineering scaffolds offer the merits of minimal invasion as well as localized and controlled biomolecule release to targeted sites. In this study, we prepared injectable hydrogel systems based on visible light-cured glycol chitosan (GC) hydrogels containing bone morphogenetic protein-2 (BMP-2) and/or transforming growth factor-beta1 (TGF-β1) as scaffolds for bone formation in vitro and in vivo. The hydrogels were characterized by storage modulus, scanning electron microscopy (SEM) and swelling ratio analyses. The developed hydrogel systems showed controlled releases of growth factors in a sustained manner for 30 days. In vitro and in vivo studies revealed that growth factor-loaded GC hydrogels have no cytotoxicity against MC3T3-E1 osteoblast cell line, improved mRNA expressions of alkaline phosphatase (ALP), type I collagen (COL 1) and osteocalcin (OCN), and increased bone volume (BV) and bone mineral density (BMD) in tibia defect sites. Moreover, GC hydrogel containing BMP-2 (10 ng) and TGF-β1 (10 ng) (GC/BMP-2/TGF-β1-10 ng) showed greater bone formation abilities than that containing BMP-2 (5 ng) and TGF-β1 (5 ng) (GC/BMP-2/TGF-β1-5 ng) in vitro and in vivo. Consequently, the injectable GC/BMP-2/TGF-β1-10 ng hydrogel may have clinical potential for dental or orthopedic applications.
Keyphrases
- tissue engineering
- transforming growth factor
- bone regeneration
- drug delivery
- bone mineral density
- epithelial mesenchymal transition
- mesenchymal stem cells
- hyaluronic acid
- wound healing
- visible light
- growth factor
- electron microscopy
- cancer therapy
- gas chromatography
- postmenopausal women
- body composition
- high resolution
- bone marrow
- oxidative stress
- signaling pathway
- single cell
- soft tissue
- mass spectrometry
- drug release
- extracellular matrix
- climate change
- binding protein
- bone loss