作者: Jae Yoon Lee , Woo-Jae Chung , GeunHyung Kim
DOI: 10.1039/C6RA07054J
关键词: Biomineralization 、 Scaffold 、 M13 bacteriophage 、 Regeneration (biology) 、 Gene expression 、 Biophysics 、 Alkaline phosphatase 、 Chemistry 、 In vitro 、 Bone tissue
摘要: Appropriate mechanical and outstanding biological properties of biomedical scaffolds are prerequisites to successfully regenerate bone tissues. Here, we designed a hybrid scaffold consisting microsized core–sheath struts based on chemically conjugated M13 bacteriophage (phage)/alginate poly(e-caprolactone) (PCL). The filamentous phages were modified with the Arg-Gly-Asp (RGD) sequence calcium-binding sites. was mesh-like core (PCL)–sheath (phage/alginate) structure (strut size = 434 ± 51 μm, pore 495 23 completely interconnected pores). To evaluate in vitro using osteoblast-like (MG63) cells, used two controls: pure alginate RGD-modified (R-A). analyzed for various activities (tensile property, protein absorption ability, biomineralization, cell responses, osteogenic gene expression). biomineralization ability significantly higher than those R-A. Furthermore, proliferation viable cells level expression (alkaline phosphatase activity) phage/alginate enhanced compared control scaffolds. Based these results, suggest that phage/PCL-based may have potential as use tissue regeneration.