Avaliação da formação de smear layer no preparo químico mecânico realizado com solução ou gel de hipoclorito de sódio a 2, 5% / Evaluation of smear layer formation in mechanical chemical preparation performed with 2. 5% sodium hypochloride solution or gel

Introdução: a formação de smear layer durante o preparo dos canais radiculares com o uso de hipoclorito de sódio solução já foi amplamente estudada; entretanto, na apresentação em gel não existem relatos na literatura. Objetivo: avaliar, em MEV, a formação de smear layer durante o preparo endodôntico, utilizando o NaOCl nas formas líquida e gel, associado ou não ao EDTA. Métodos: sessenta raízes palatinas de molares superiores ou distais de inferiores, com comprimento radicular padronizado em 15 mm, foram utilizadas. As amostras foram divididas em quatro grupos controle com n = 5 cada (soro fisiológico ou base gel, associados ou não ao EDTA) e quatro grupos testes com n = 10 cada, de acordo com a substância irrigadora empregada durante o preparo (solução ou gel de NaOCl a 2,5%, associados ou não ao EDTA). Os canais foram modelados e posteriormente clivados para análise em MEV (ampliação de 2000x). Imagens de eletromicrografias foram obtidas nos terços cervical, médio e apical. A presença e as características da smear layer formadas foram categorizadas. As imagens foram analisadas por dois avaliadores, previamente, calibrados. Após a análise de concordância (Kappa = 0,806) dos escores, os dados foram tratados com o uso do teste Kruskall-Wallis, complementado pelo teste de Comparações Múltiplas SNK. O nível de significância foi de 5%. Resultados: a utilização do soro fisiológico e do NaOCl líquido, associados à irrigação final com EDTA, apresentou os melhores resultados de limpeza. Com o uso do NaOCl gel e da base gel, sem associação ao EDTA, houve uma maior quantidade de resíduos sobre as paredes dentinárias. Além disso, independentemente da substância irrigadora testada, pode-se observar que houve uma melhor capacidade de remoção da smear layer no terço cervical em relação ao apical. Conclusões: observou-se formação de smear layer após o preparo do canal radicular associado ao NaOCl líquido ou gel. A aplicação de EDTA promoveu a remoção da smear layer produzida durante o preparo do canal.

Introduction: the formation of smear layer during the preparation of root canals with the use of sodium hypochlorite solution has been widely studied; however, in the gel presentation there aren't reports in the literature. Objective: to evaluate, in SEM, the formation of smear layer during endodontic preparation, using NaOCl in liquid and gel forms, associated or not with EDTA. Methods: sixty palatal roots of maxillary molars or distal roots of lower molars, with a root length of 15 mm, were used. The samples were divided into four control groups with n = 5 each (saline or gel base, associated or not with EDTA) and four test groups (n = 10 each) according to the irrigation substance used during the preparation (2.5% NaOCl solution or gel, associated or not with EDTA). The root canals were instrumented and later split for SEM analysis (2000x magnification). Electromicrographic images were obtained from the cervical, middle and apical thirds. The presence and characteristics of the smear layer formed were categorized. The images were analyzed by two previously calibrated evaluators. After the Kappa analysis (0.806), the data were treated using the Kruskall-Wallis test, complemented by the SNK Multiple Comparison Test. The level of significance was 5%. Results: the use of saline and liquid NaOCl, associated with final rinsing with EDTA, showed the best cleaning results. With the use of NaOCl gel and gel base, with no EDTA association, there was a greater amount of residues on the dentin surfaces. In addition, despite the irrigation substance tested, it can be observed that there was a better capacity of removal of the smear layer in the cervical third in relation to the apical. Conclusion: root canal instrumentation associated with NaOCl solution or gel EDTA produced smear layer. Smear layer was removed with the use of EDTA as a final flushing.

Evaluation of the Toxicity of Silver/Silica and Titanium Dioxide Particles in Mammalian Cells

ABSTRACT The increasing concern over the spread of diseases has lead to a high consumption of antimicrobial additives in the medical and industrial fields. Since these particles can lixiviate from loaded materials, the contact between this additive and mammalian cells can occur during manufacture, use and disposal of the products. Silver on fumed silica (AgNP_SiO2) and titanium dioxide (TiO2) can be used as antimicrobial additives that are applied in polymeric formulation. While these additives can inhibit bacteria, fungus and virus proliferation; they may also be harmful to humans. Standard toxicological studies were undertaken using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide), CBPI (cytokinesis-block proliferation index) and micronucleus assay using different sets of additive concentrations. The nanosize of the samples evaluated was confirmed by transmission electronic microscopy. No significant micronucleus frequency increase or cell viability reduction were observed with the exposure of L-929 murine fibroblast cells to AgNP_SiO2 and TiO2 particles at any of the tested concentrations. The non toxic effect of the analyzed particles can be explained by considering its agglomeration tendency, composition, and crystalline form. Further investigations should be done to understand the interference of agglomeration and how it affects the toxicological study.