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1.
Minerva Stomatol ; 50(3-4): 91-100, 2001.
Artigo em Italiano | MEDLINE | ID: mdl-11378644

RESUMO

At the moment, in most countries, there are laws in force which impose to the manufacturers well regulated testing in order to investigate and guarantee an acceptable biocompatibility of medical devices before their commercialization. Many international laboratories are committed to the definition of investigation methodologies and to the evaluation of biocompatibility in order to obtain research standards, capable to provide reproducible and comparable objective quantitative data. In every country, technical committees were put together for a standardization of methodological procedures, followed by European and international technical boards which proposed and codified methodologies and investigation approaches. UNI-EN-ISO laws contain all the results and constitute a reference point for any consideration on or evaluation of the biocompatibility of a medical device. Based on these laws, we evaluated the biocompatibility and determined the physical-mechanical characteristics of the new Venezia (Cabon S.p.A.) endodontic ZOE sealer. The Subcutaneous Implant Technique according Safavi et al. (in vivo test, ISO 10993: 1-6 Biological evaluation of medical and dental materials and devices) and Autian test of Emolysis on Rabbit Erythrocytes (in vitro test) allowed us to evaluate a good biocompatibility of the new product. Furthermore, its Setting and Working time, its radiopacity, Solubility and its Flow value completely satisfy the requirements of international standards (ISO/DIS 6876 Dental root Canal Sealing Materials). We can finally deduce that Venezia fulfil the ideal functional properties of an endodontic cements.


Assuntos
Materiais Biocompatíveis , Cimentos Dentários , Materiais Restauradores do Canal Radicular , Animais , Masculino , Teste de Materiais , Coelhos , Ratos , Ratos Wistar
2.
Minerva Stomatol ; 48(7-8): 307-10, 1999.
Artigo em Italiano | MEDLINE | ID: mdl-10568106

RESUMO

BACKGROUND: The aim of this study was to evaluate the presence of Russell bodies in chronically inflamed pulp using histological methods. METHODS: The authors analysed 20 samples: 18 were teeth or pulp from subjects suffering from chronic pulpar diseases and 2 were teeth extracted for orthodontic reasons showing no signs of pulpar disease. RESULTS: Russell bodies were found in the majority of samples examined, both inside the plasma cells and in pulpar stroma. Russell bodies were not present in samples affected by acute phlogistic processes, with a prevalence of neutrophil granulocytes in the pulp structure, and not in elements free from pulpar disease. CONCLUSIONS: As already reported in earlier studies of periapical lesions, also in this case the irritative stimulus caused by the bacteria present in chronically inflamed pulp leads to the hyperactivation of plasma cells and the consequent hyperproduction of immunoglobulins.


Assuntos
Pulpite/patologia , Doença Crônica , Humanos , Plasmócitos/patologia
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