Lithograph-moulded poly-L-co-D,L lactide porous membranes for osteoblastic culture
A. D. Messias, D. C. Coraca-Huber, C. Lucchesi, A. Pavani, E. A. R. Duek
ARTIGO
Inglês
Agradecimentos: The authors thank the technicians of the Faculty of Mechanical Engineering and of the Electron Microscopy Laboratory of the Institute of Biology, UNICAMP, for help in this investigation, and Dr. Stephen Hyslop for the English review of the manuscript. This work was supported by...
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Agradecimentos: The authors thank the technicians of the Faculty of Mechanical Engineering and of the Electron Microscopy Laboratory of the Institute of Biology, UNICAMP, for help in this investigation, and Dr. Stephen Hyslop for the English review of the manuscript. This work was supported by FAPESP. The authors have no conflicts of interest with this work
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Pore size, shape, wall morphology, porosity, and interconnectivity are important characteristics of the scaffolds. Lithography is a manufacturing technique that allows the production of tridimensional scaffolds with a controllable and reproducible inner architecture. The aim of this study was to use...
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Pore size, shape, wall morphology, porosity, and interconnectivity are important characteristics of the scaffolds. Lithography is a manufacturing technique that allows the production of tridimensional scaffolds with a controllable and reproducible inner architecture. The aim of this study was to use lithography to create a poly-L-co-D,L lactide (PLDLA) scaffold with symmetrical pore size and distribution, and to evaluate its biocompatibility with osteoblasts in vitro. Lithographic moulds were used to produce porous PLDLA membranes by a casting procedure. Osteoblasts were removed from calvarial bones and seeded onto porous and smooth PLDLA membranes after which cell viability and adhesion assays, cytochemical analysis and scanning electron microscopy were used to characterize the cells. Cell viability and adhesion assays, cytochemical analysis, and scanning electron microscopy were carried out. Cell viability was similar on porous and smooth PLDLA membranes but higher than on a polystyrene substrate (positive control). Although osteoblasts adhered to the surface of all the materials tested, cell adhesion to lithographed PLDLA was greater than to smooth PLDLA membranes. In conclusion, osteoblasts interacted well with PLDLA membranes, as shown by the viability and adhesion assays and by the enhanced collagen production
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Aberto
Lithograph-moulded poly-L-co-D,L lactide porous membranes for osteoblastic culture
A. D. Messias, D. C. Coraca-Huber, C. Lucchesi, A. Pavani, E. A. R. Duek
Lithograph-moulded poly-L-co-D,L lactide porous membranes for osteoblastic culture
A. D. Messias, D. C. Coraca-Huber, C. Lucchesi, A. Pavani, E. A. R. Duek
Fontes
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Materials research. Ibero-american journal of materials (Fonte avulsa) |