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1.
ScientificWorldJournal ; 2014: 905103, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25298970

RESUMO

The in vivo biocompatibility and toxicity of PVA/NOCC scaffold were tested by comparing them with those of a biocompatible inert material HAM in a rat model. On Day 5, changes in the blood parameters of the PVA/NOCC-implanted rats were significantly higher than those of the control. The levels of potassium, creatinine, total protein, A/G, hemoglobulin, erythrocytes, WBC, and platelets were not significantly altered in the HAM-implanted rats, when compared with those in the control. On Day 10, an increase in potassium, urea, and GGT levels and a decrease in ALP, platelet, and eosinophil levels were noted in the PVA/NOCC-implanted rats, when compared with control. These changes were almost similar to those noted in the HAM-implanted rats, except for the unaltered potassium and increased neutrophil levels. On Day 15, the total protein, A/G, lymphocyte, monocyte, and eosinophil levels remained unaltered in the PVA/NOCC-implanted rats, whereas urea, A/G, WBC, lymphocyte, and monocyte levels remained unchanged in the HAM-implanted rats. Histology and immunohistochemistry analyses revealed inflammatory infiltration in the PVA/NOCC-implanted rats, but not in the HAM-implanted rats. Although a low toxic tissue response was observed in the PVA/NOCC-implanted rats, further studies are necessary to justify the use of this material in tissue engineering applications.


Assuntos
Materiais Biocompatíveis/química , Quitosana/química , Álcool de Polivinil/química , Engenharia Tecidual/métodos , Alicerces Teciduais/química , Fosfatase Alcalina/sangue , Âmnio/metabolismo , Animais , Antígenos CD/metabolismo , Antígenos de Diferenciação Mielomonocítica/metabolismo , Materiais Biocompatíveis/farmacologia , Contagem de Células Sanguíneas , Feminino , Humanos , Hidrogéis , Imuno-Histoquímica , Implantes Experimentais , Masculino , Potássio/sangue , Ratos Sprague-Dawley , Pele/efeitos dos fármacos , Pele/metabolismo , Transplante de Pele/métodos , Tela Subcutânea/efeitos dos fármacos , Tela Subcutânea/metabolismo , Tela Subcutânea/cirurgia , Fatores de Tempo , Transplante Heterólogo , Ureia/sangue , gama-Glutamiltransferase/sangue
2.
Int J Med Sci ; 10(12): 1608-14, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24151432

RESUMO

The objective of this study was to compare the morphological and chemical composition of bone graft (BG) and coral graft (CG) as well as their osteogenic differentiation potential using rabbit mesenchymal stem cells (rMSCs) in vitro. SEM analysis of BG and CG revealed that the pores in these grafts were interconnected, and their micro-CT confirmed pore sizes in the range of 107-315 µm and 103-514 µm with a total porosity of 92% and 94%, respectively. EDS analysis indicated that the level of calcium in CG was relatively higher than that in BG. FTIR of BG and CG confirmed the presence of functional groups corresponding to carbonyl, aromatic, alkyl, and alkane groups. XRD results revealed that the phase content of the inorganic layer comprised highly crystalline form of calcium carbonate and carbon. Atomic force microscopy analysis showed CG had better surface roughness compared to BG. In addition, significantly higher levels of osteogenic differentiation markers, namely, alkaline phosphatase (ALP), Osteocalcin (OC) levels, and Osteonectin and Runx2, Integrin gene expression were detected in the CG cultures, when compared with those in the BG cultures. In conclusion, our results demonstrate that the osteogenic differentiation of rMSCs is relatively superior in coral graft than in bone graft culture system.


Assuntos
Antozoários/citologia , Transplante Ósseo/métodos , Técnicas de Cultura de Células , Células-Tronco Mesenquimais/citologia , Osteogênese/efeitos dos fármacos , Fosfatase Alcalina/biossíntese , Animais , Antozoários/química , Materiais Biocompatíveis/isolamento & purificação , Materiais Biocompatíveis/metabolismo , Cálcio/isolamento & purificação , Cálcio/metabolismo , Diferenciação Celular/efeitos dos fármacos , Proliferação de Células , Sobrevivência Celular , Regulação da Expressão Gênica , Células-Tronco Mesenquimais/efeitos dos fármacos , Células-Tronco Mesenquimais/metabolismo , Microscopia de Força Atômica , Osteocalcina/biossíntese , Coelhos
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