Cyclic fatigue resistance of ProTaper Universal instruments when subjected to static and dynamic tests.

OBJECTIVE: This study evaluated the number of cycles to fracture of ProTaper Universal S2 instruments when subjected to static and dynamic cyclic fatigue tests. STUDY DESIGN: ProTaper Universal S2 instruments were used until fracture in an artificial curved canal under rotational speed of 300 rpm in either a static or a dynamic test model. Afterward, the length of the fractured segments was measured and fractured surfaces and helical shafts analyzed by scanning electron microscopy (SEM). RESULTS: The number of cycles to fracture was significantly increased when instruments were tested in the dynamic model (P<.001). Instrument separation occurred at the point of maximum flexure within the artificial canals, i.e., the midpoint of the curved canal segment. SEM analysis revealed that fractured surfaces exhibited characteristics of the ductile mode. Plastic deformation was not observed in the helical shaft of fractured instruments. CONCLUSIONS: The number of cycles to fracture ProTaper Universal S2 instruments significantly increased with the use of instruments in a dynamic cyclic fatigue test compared with a static model. These findings reinforce the need for performing continuous pecking motions during rotary instrumentation of curved root canals.

Comparison of the effectiveness of three irrigation techniques in reducing intracanal Enterococcus faecalis populations: an in vitro study.

INTRODUCTION: Several irrigation techniques have been recently introduced with the main objective of improving root canal disinfection. This in vitro study aimed at comparing the intracanal bacterial reduction promoted by chemomechanical preparation with 3 different irrigation techniques. METHODS: Root canals from extracted teeth were contaminated with Enterococcus faecalis ATCC 29212 for 7 days and then randomly distributed into 3 experimental groups of 20 teeth each: group 1, conventional irrigation with NaviTip needles inserted up to 3 mm short of the working length; group 2, same as group 1, but supplemented with final irrigant activation by the EndoActivator system; and group 3, irrigation with the EndoVac system. NaOCl and ethylenediaminetetraacetic acid (EDTA) were the irrigants used in all experimental groups. The overall preparation time was kept constant for the groups, but the total volume ranged from 20 mL (groups 1 and 2) to 43 mL (group 3). The control group was irrigated with saline solution (total volume, 43 mL). Samples taken before and after chemomechanical procedures were cultured, and the colony-forming units (CFUs) were counted. RESULTS: Reduction in the bacterial populations was highly significant for all groups. The 3 experimental groups with NaOCl and EDTA as irrigants were significantly more effective than the control group with saline in reducing CFU counts. There were no significant differences between the 3 techniques tested. CONCLUSIONS: There was no evident antibacterial superiority of any of the irrigation techniques evaluated in the present in vitro model.

On the use of denaturing gradient gel electrophoresis approach for bacterial identification in endodontic infections.

Bacteria in infected root canals of teeth evincing chronic apical periodontitis lesions were identified by a polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) approach. DNA was extracted from root canal samples, and part of the 16S rRNA gene of all bacteria was amplified by PCR and separated by DGGE, generating banding patterns representative of the community structure. Twenty visible bands were cut out of the gel, re-amplified, and sequenced to provide identification. Sequencing analysis revealed the presence of both cultivable and as-yet-uncultivated species in the samples analyzed, including representatives of the genera Fusobacterium, Bacteroides, Dialister, Synergistes, Prevotella, Eubacterium and Peptostreptococcus. Unambiguous identification was not always possible and the method's limitations are discussed. In general, the findings showed that PCR-DGGE can be useful for the identification of both cultivable and as-yet-uncultivated bacteria in endodontic infections.