Bioactive polymer composite scaffolds fabricated from 3D printed negative molds enable bone formation and vascularization

被引:6
作者
Du, Shengrong [1 ,2 ]
Huynh, Tony [1 ]
Lu, Yen-Zhen [3 ]
Parker, Bradyn J. [1 ,2 ]
Tham, Stephen K. [4 ]
Thissen, Helmut [2 ]
Martino, Mikael M. [3 ,5 ]
Cameron, Neil R. [1 ,6 ,7 ]
机构
[1] Monash Univ, Dept Mat Sci & Engn, 14 Alliance Lane, Clayton, VIC 3800, Australia
[2] CSIRO Mfg Res Way, Clayton, Vic 3168, Australia
[3] Monash Univ, Australian Regenerat Med Inst, European Mol Biol Lab Australia, Clayton, Vic 3800, Australia
[4] Monash Univ, Dept Surg, 246 Clayton Rd, Clayton, Vic 3168, Australia
[5] Monash Univ, Victorian Heart Inst, Clayton, Vic 3800, Australia
[6] Univ Warwick, Sch Engn, Coventry CV4 7AL, England
[7] Univ Malaya, Nanotechnol & Catalysis Res Ctr NANOCAT, Kuala Lumpur 50603, Malaysia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
PolyHIPEs; 3D printing; Microchannels; Vascularization; Bone regeneration; TISSUE ENGINEERING SCAFFOLDS; EMULSION-TEMPLATED SCAFFOLDS; MECHANICAL-PROPERTIES; CALVARIAL DEFECTS; TRABECULAR BONE; CELL-CULTURE; BIOMATERIALS; NETWORKS; POROSITY; MODELS;
D O I
10.1016/j.actbio.2024.07.038
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Scaffolds for bone defect treatment should ideally support vascularization and promote bone formation, to facilitate the translation into biomedical device applications. This study presents a novel approach utilizing 3D-printed water-dissolvable polyvinyl alcohol (PVA) sacrificial molds to engineer polymerized High Internal Phase Emulsion (polyHIPE) scaffolds with microchannels and distinct multiscale porosity. Two sacrificial mold variants (250 mu m and 500 mu m) were generated using fused deposition modeling, filled with HIPE, and subsequently dissolved to create polyHIPE scaffolds containing microchannels. In vitro assessments demonstrated significant enhancement in cell infiltration, proliferation, and osteogenic differentiation, underscoring the favorable impact of microchannels on cell behavior. High loading efficiency and controlled release of the osteogenic factor BMP-2 were achieved, with microchannels facilitating release of the growth factor. Evaluation in a mouse critical-size calvarial defect model revealed enhanced vascularization and bone formation in microchanneled scaffolds containing BMP-2. This study not only introduces an accessible method for creating multiscale porosity in polyHIPE scaffolds but also emphasizes its capability to enhance cellular infiltration, controlled growth factor release, and in vivo performance. The findings suggest promising applications in bone tissue engineering and regenerative medicine, and are expected to facilitate the translation of this type of biomaterial scaffold.
引用
收藏
页码:260 / 274
页数:15
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