Antimicrobial action of photodynamic therapy in root canals using LED curing light, curcumin and carbopol gel.

AIM: To evaluate the capacity of carbopol gel to maintain the intensity of a LED curing light (blueLED) along the length of prepared root canals in bovine teeth, and to assess the antimicrobial capacity of curcumin photoactivated by a LED curing light in the presence of carbopol gel. METHODOLOGY: Experiment 1: Eight straight roots of bovine incisors were standardized to a length of 15 mm, and the root canals instrumented up to a size 120 K-file. The LED curing light was irradiated inside the root canals using an aluminium collimator (1.5 mm in diameter) placed at the orifice (n = 8). Initially, the irradiation was performed in empty root canals and then repeated with the root canals filled with carbopol gel. Simple standardized photographs of the roots were taken with a digital camera in the mesial perspective during the irradiation procedure and the images analysed in OriginLab software to verify the light intensity along the length of the root. Experiment 2: Twenty dentine blocks were obtained from the cervical third of bovine incisors using a trephine bur. Biofilms were induced for 21 days on the blocks using Enterococcus faecalis (ATCC 4083) at 109 cells mL-1 . The blocks were treated according to the groups (n = 5): positive control; standard PDT (methylene blue + diode Laser); curcumin; LED curing light; and curcumin + LED curing light. After the treatment, the samples were dyed with Live/Dead BacLight Bacterial Viability solution and fluorescence images were obtained by Confocal Scanning Laser Microscopy (CSLM). Experiment 3: Thirty-two roots of bovine incisors were prepared as described in experiment 1. Their dentinal tubules were contaminated and the root canals treated according to the groups (n = 8): positive control; standard PDT; curcumin + LED curing light; curcumin + carbopol gel + LED curing light. The specimens were sectioned longitudinally and the split roots were treated with the Live/Dead dye to obtain fluorescence images by CSLM. All images were processed using BioImageL software to measure the percentage of viable bacteria and the data analysed statistically using the nonparametric Kruskal-Wallis test (α < 0.05). RESULTS: In Experiment 1, carbopol gel did not improve the intensity of LED light transmission along the root canal. In Experiment 2, a significant decrease (P < 0.05) in bacterial viability occurred in the following order: positive control < only LED curing light < only curcumin < curcumin + LED curing light = standard PDT; and in Experiment 3 positive control = curcumin + LED curing light ≤ curcumin + gel + LED curing light ≤ standard PDT. CONCLUSION: Similar disinfection effectiveness was obtained using curcumin + LED curing light and methylene blue + 660 nm LASER (standard PDT). The use of carbopol gel did not favour a greater transmission of LED light along the root canal and also resulted in less bacterial killing when used in endodontic PDT.

Evaluation of vascular effect of Photodynamic Therapy in chorioallantoic membrane using different photosensitizers.

Photodynamic Therapy (PDT) is a local treatment that requires a photosensitizing agent, light and molecular oxygen. With appropriate illumination, the photosensitizer is excited and produces singlet oxygen that is highly reactive and cytotoxic. Tumor vascular network is essential for the tumor growth and the understanding of vascular response mechanisms enables an improvement in the PDT protocol for cancer treatment. Compounds of porphyrin (Photogem®) and chlorin (Photodithazine®) were the photosensitizers tested. The incubation times varied from 20 to 80 min and the concentration ranged between 0.1 and 100 µg/cm(2). Different light doses were used between 4.8 and 40 J/cm(2) with irradiance varying between 80 and 100 mW/cm(2). The light dose of 30 J/cm(2) was used in the intravenous photosensitizer application. The membrane images were made from 0 to 300 min after treatment. The vascular response was evaluated by the average vessel area. Different responses was observed depending on the photosensitizer concentration and administration form. Intravenous application has been more efficient to produce vessel constriction and the most pronounced effect was observed for the chlorin.

Temperature response in the pulpal chamber of primary human teeth exposed to Nd:YAG laser using a picosecond pulsed regime.

OBJECTIVE: This study was conducted to analyze temperature variation in the pulpal chamber using the (Nd:YAG) picosecond-pulsed laser to promote ablation in enamel and dentin of primary teeth. BACKGROUND DATA: Several previous studies reported the temperature rise in pulpal chamber during laser irradiation. Since there are no reports about pulp chamber temperature changes during irradiation with picosecond-pulsed laser, the purpose of our investigation is to quantify the intrapulpal temperature changes following picosecond-pulsed Nd:YAG laser irradiation of enamel and dentin of primary teeth. METHODS: In this study, we used 10 intact primary exfoliated teeth: five molars and five incisors. We used a commercial neodymium:- yttrium-aluminum-garnet continuous-wave (CW)-pumped Q-switched and mode-locked Nd:YAG laser, with varying power levels (200, 300, and 350 mW) operating with 100-psec pulsed duration. RESULTS: Typical plots show differences between heating and cooling of enamel and dentin of anterior and posterior teeth. Whereas for enamel the time evolution curves are dependent on power used for the investigated range (200-350 mW), for dentin the differences are not so evident. Observing temperature enhancement for each power, we were able to analyze operational conditions where temperature changes do not exceed 5.5 degrees C. Power-time-temperature (PTT) diagrams for clinical operations were determined based on varying power level and exposition time. Through the heating-cooling cycle, we could extract conventional heating and cooling times for enamel and dentin. CONCLUSION: We have shown that the Nd:YAG picosecond-pulsed laser is a safe tool for ablation of primary teeth in a broad range of operational parameters.