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The purpose of this in vitro study was to observe the morphological changes and apical dye penetration at apical dentin surfaces after apicoectomy with conventional techniques and laser beam. Sixty single-rooted extracted teeth were selected for the study. The crowns were resected below the cemento-enamel junction. Then, these teeth were treated endodontically and filled with gutta-percha using AH-26 root canal sealer. The teeth were randomly divided into four groups of 15 teeth in each. The roots were resected perpendicular to its long axis 3 mm from the apex using Er: yttrium-aluminium-garnet (YAG) laser irradiation in groups 1 and 2, and the resected root surfaces were lased with Nd:YAG laser in group 2. The apexes were resected by a high-speed handpiece in groups 3 and 4, and the resected root surfaces were lased with Nd:YAG laser in group 4. Ten teeth in each group were used for leakage studies, and the other five teeth were used for scanning electron microscopic examinations. Seven sections were obtained from each root to assess the microleakage, and the sections were analyzed in a computer-assisted manner. No statistically significant differences were observed between the leakage percentage of groups 1 and 3 and groups 2 and 4 (p>0.05). Morphological differences were observed between apical dentin surfaces resected with conventional techniques and laser beam.

The application of Nd:YAG lasers in endodontics has been explored by many investigators for different purposes. The aim of this in vitro study is to evaluate the effects of Nd:YAG laser on osteoblast cell cultures. A 1,064 nm Nd:YAG laser was used to irradiate human osteoblast-like cells (Saos-2) in noncontact mode for 10 s with different energy settings. The settings varied were pulse energy (20-120 mJ), pulse repetition rate (10-30 Hz), and power output (0.2-3.6 W). He-Ne, the aiming beam of Nd:YAG laser, was used in noncontact mode for 10 s. After 7-, 14-, and 21-day incubation period, cell viability and proliferation were evaluated with methylthiazoletetrazolium (MTT) colorometric method. The comparison of average MTT values gave no statistically significant difference between 20 mJ, 10 Hz, He-Ne, and control (p < 0.05). The differences between all other groups were significant (p < 0.05). Increase in the pulse energy, pulse repetition rate, and power output has a negative effect on the cell viability and proliferation.