1. Electrospun ultrathin PBAT/nHAp fibers influenced the in vitro and in vivo osteogenesis and improved the mechanical properties of neoformed bone
- Author
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Edmundo Silva, Anderson Oliveira Lobo, Bruno V.M. Rodrigues, Luana Marotta Reis de Vasconcellos, Gabriela de Fátima Santana-Melo, Ritchelli Ricci, Thomas J. Webster, Fernanda Roberta Marciano, Universidade Estadual Paulista (Unesp), Univ Brasil, Univ Vale Paraiba, Harvard Med Sch, and Northeastern Univ
- Subjects
Male ,Bone Regeneration ,Polyesters ,Nanofibers ,Gene Expression ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Bone and Bones ,Colloid and Surface Chemistry ,Flexural strength ,Osteogenesis ,In vivo ,Cell Line, Tumor ,Animals ,Humans ,PBAT ,Physical and Theoretical Chemistry ,Bone regeneration ,Micro-computed tomography ,Osteoblasts ,Electrospinning ,Tibia ,Tissue Scaffolds ,Chemistry ,Nanohydroxyapatite ,Electric Conductivity ,In vitro toxicology ,Surfaces and Interfaces ,General Medicine ,Anatomy ,021001 nanoscience & nanotechnology ,Electroplating ,In vitro ,Rats ,0104 chemical sciences ,Polyester ,Durapatite ,Nanofiber ,Gene expression ,0210 nano-technology ,Biotechnology ,Biomedical engineering - Abstract
Made available in DSpace on 2018-11-26T17:34:51Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-07-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Brazilian Innovation Agency (FINEP) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Combining polyester scaffolds with synthetic nanohydroxyapatite (nHAp), which is bioactive and osteoconductive, is a plausible strategy to improve bone regeneration. Here, we propose the combination of PBAT [poly(butylene-adipate-co-terephthalate)] and synthetic nHAp (at 3 and 5 wt%). PBAT is a relatively a new polymer with low crystallinity and attractive biodegradability and mechanical properties for orthopedic applications, however, with a still underexplored potential for in vivo applications. Then, we performed a careful biological in vitro and in vivo set of experiments to evaluate the influence of PBAT containing two different nHAp loads. For in vitro assays, osteoblast-like MG63 cells were used and the bioactivity and gene expression related to osteogenesis were evaluated by qRT-PCR. For in vivo experiments, twenty-four male rats were used and a tibial defect model was applied to insert the scaffolds. Micro-computed tomography (Micro-CT) and histological analysis were used to assess e bone neoformation after 6 weeks of implantation. Three point flexural tests measured the mechanical properties of the neoformed bone. All scaffolds showed promising in vitro properties, since they were not cytotoxic against MG-63 cells and promoted high cell proliferation and formation of mineralized nodules. From a mechanistic point-of-view, nHAp loading increased hydrophilicity, which in turn allowed for a better adsorption of proteins and consequent changes in the phenotypic expression of osteoblasts. nHAp induced better cellular responses on/in the scaffolds, which was mainly attributed to its osteoconductive and osteoinductive properties. Micro-CT images showed that nHAp at 3% and 5 wt% led to more effective bone formation, presenting the highest bone volume after 6 weeks of implantation. Considering the three point flexural tests, 5 wt% of nHAp positively influenced the flexural mode of the neoformed bone, but the stiffness was similar between the 3% and 5 wt% groups. In summary, this investigation demonstrated great potential for the application of these novel scaffolds towards bone regeneration and, thus, should be further studied. (C) 2017 Elsevier B.V. All rights reserved, Sao Paulo State Univ, Inst Sci & Technol, Dept Biosci & Oral Diag, Sao Jose Dos Campos, SP, Brazil Univ Brasil, Lab Biomed Nanotechnol, Itaquera, SP, Brazil Univ Vale Paraiba, Inst Res & Dev IP&D, Lab Biomed Nanotechnol, Sao Jose Dos Campos, SP, Brazil Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Biomat Innovat Res Ctr, Cambridge, MA USA Northeastern Univ, Dept Chem Engn, Nanomed Lab, Boston, MA 02115 USA Sao Paulo State Univ, Inst Sci & Technol, Dept Biosci & Oral Diag, Sao Jose Dos Campos, SP, Brazil FAPESP: 2011/17877-7 FAPESP: 2011/20345-7 FAPESP: 2015/09697-0 FAPESP: 2016/00575-1 CNPq: 474090/2013-2 Brazilian Innovation Agency (FINEP): 0113042800 CAPES: 88887.095044/2015-00 FAPESP: 2015/08523-8
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- 2017
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