Please use this identifier to cite or link to this item: https://doi.org/10.1177/0885328208094301
Title: Proliferation and differentiation of human osteoblasts within 3D printed poly-lactic-co-glycolic acid scaffolds
Authors: Ge, Z. 
Wang, L.
Heng, B.C. 
Tian, X.-F.
Lu, K.
Fan, V.T.W. 
Yeo, J.F. 
Cao, T. 
Tan, E. 
Keywords: 3D printing
Osteoblast
Osteogenesis
Scaffold
Issue Date: 2009
Source: Ge, Z., Wang, L., Heng, B.C., Tian, X.-F., Lu, K., Fan, V.T.W., Yeo, J.F., Cao, T., Tan, E. (2009). Proliferation and differentiation of human osteoblasts within 3D printed poly-lactic-co-glycolic acid scaffolds. Journal of Biomaterials Applications 23 (6) : 533-547. ScholarBank@NUS Repository. https://doi.org/10.1177/0885328208094301
Abstract: Bone repair and regeneration can be enhanced through implantation of biocompatible and biodegradable scaffolds, which serve primarily as osteoconductive moieties. In this study, the mechanical properties and microenviroment of 3D printed poly-lactic-co-glycolic acid (PLGA) scaffolds are examined. Additionally, the proliferation and differentiation of human fetal osteoblasts are evaluated after 3 weeks of in vitro culture on the scaffolds. The results showed that the PLGA scaffolds examined had mechanical properties similar to that of trabecular bone, but was still much weaker compared to cortical bone. In addition to general porosity, the PLGA scaffolds also had micropores within macropore walls. Cultured human osteoblasts could proliferate upon seeding on the PLGA scaffolds. Alkaline phosphatase activity and osteonectin expression of the osteoblasts cultured on the PLGA scaffolds remained stable over three weeks, whilst expression of collagen type I and osteopontin decreased. The alkaline phosphatase activity of osteoblasts cultured on PLGA scaffolds is comparable with that from two commercially-available scaffolds - OPLA and collagen scaffolds (Becton-Dickinson (BD) Inc., Franklin Lakes, NJ, USA). Hence, the results suggested that the PLGA scaffolds examined are conducive for promoting osteogenesis. © SAGE Publications, Inc. 2009.
Source Title: Journal of Biomaterials Applications
URI: http://scholarbank.nus.edu.sg/handle/10635/67240
ISSN: 08853282
DOI: 10.1177/0885328208094301
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