QMix® irrigant reduces lipopolysacharide (LPS) levels in an in vitro model

AbstractThe presence of endotoxin inside the root canal has been associated with periapical inflammation, bone resorption and symptomatic conditions.Objectives To determine, in vitro, the effect of QMix® and other three root canal irrigants in reducing the endotoxin content in root canals.Material and Methods Root canals of single-rooted teeth were prepared. Samples were detoxified with Co-60 irradiation and inoculated with E. coli LPS (24 h, at 37°C). After that period, samples were divided into 4 groups, according to the irrigation solution tested: QMix®, 17% EDTA, 2% chlorhexidine solution (CHX), and 3% sodium hypochlorite (NaOCl). LPS quantification was determined by Limulus Amebocyte Lysate (LAL) assay. The initial counting of endotoxins for all samples, and the determination of LPS levels in non-contaminated teeth and in contaminated teeth exposed only to non-pyrogenic water, were used as controls.Results QMix® reduced LPS levels, with a median value of 1.11 endotoxins units (EU)/mL (

Effectiveness of rotary or manual techniques for removing a 6-year-old filling material

The aim of this study was to evaluate the effectiveness of manual and rotary instrumentation techniques for removing root fillings after different storage times. Twenty-four canals from palatal roots of human maxillary molars were instrumented and filled with gutta-percha and zinc-oxide eugenol-based sealer (Endofill) , and were stored in saline for 6 years. Non-aged control specimens were treated in the same manner and stored for 1 week. All canals were retreated using hand files or ProTaper Universal NiTi rotary system. Radiographs were taken to determine the amount of remaining material in the canals. The roots were vertically split, the halves were examined with a clinical microscope and the obtained images were digitized. The images were evaluated with AutoCAD software and the percentage of residual material was calculated. Data were analyzed with two-way ANOVA and Tukey's test at 5% significance level. There was no statistically significant differences (p&gt;0.05) between the manual and rotary techniques for filling material removal regardless the ageing effect on endodontic sealers. When only the age of the filling material was analyzed microscopically, non-aged fillings that remained on the middle third of the canals presented a higher percentage of material remaining (p<0.05) compared to the aged sealers and to the other thirds of the roots. The apical third showed a higher percentage of residual filling material in both radiographic and microscopic analysis when compared to the other root thirds. In conclusion, all canals presented residual filling material after endodontic retreatment procedures. Microscopic analysis was more effective than radiographs for detection of residual filling material.O objetivo deste estudo foi avaliar a efetividade da instrumentação manual e rotatória na remoção de material obturador de canais radiculares de raízes palatinas de molares superiores humanos, em dois períodos de tempo. Vinte e quatro raízes foram instrumentadas e obturadas com guta-percha, cimento de óxido de zinco e eugenol e armazenadas em solução salina durante 6 anos. Outras 24 raízes foram tratadas da mesma maneira e armazenadas por uma semana. Os canais radiculares foram retratados usando limas manuais ou instrumentos rotatórios do Sistema ProTaper Universal. Radiografias periapicais foram feitas para mensurar a quantidade de material remanescente. Posteriormente as raízes foram clivadas e imagens microscópicas obtidas a partir de um microscópio clínico operatório foram digitalizadas. As imagens foram avaliadas através do software Autocad 2004 e área de material obturador remanescente foi mensurada. A Análise da Variância (Two-way) e o Teste T demonstraram não haver diferenças estatisticamente significantes entre a técnica manual e rotatória na remoção de material obturador. O terço apical mostrou a maior percentagem de remanescentes de material obturador, na análise radiográfica e microscópica quando comparado com os outros terços radiculares. Todos os canais revelaram resíduos de material obturador após o retratamento endodôntico. A análise microscópica foi mais efetiva do que a radiográfica na detecção de remanescente de obturação do canal radicular

Evaluation of dental autoclave sterilization through biological monitoring

O objetivo deste estudo foi avaliar a ocorrência de esterilização em autoclaves de consultórios odontológicos, mediante o emprego de indicadores biológicos, assim como, através de questionário, conhecer a prática clínica do processamento do instrumental contaminado. Foram introduzidos em 40 autoclaves, juntamente com o instrumental, três indicadores biológicos (próximo ao filtro, no centro e junto à porta). Após, os indicadores (testes e controle) foram incubados por 48h, para aferição do meio de cultura. Os indicadores-teste apresentaram mudança da cor do meio de cultura de roxo para amarelo em 14 (35%) das autoclaves. A maioria dos cirurgiões-dentista (CDs) associa ao calor úmido, outros métodos de esterilização, como o químico e o calor seco. Nenhum CD emprega rotineiramente o monitoramento biológico em seu consultório. Dos 31 CDs (77,5%) que empregam o controle físico e/ou químico da esterilização, apenas 74,2% dos mesmos, o fazem a cada ciclo. A grande maioria dos Cds (75%) emprega o envelope para o empacotamento do instrumental. No entanto, 77,5% dos mesmos não escrevem na embalagem a data da esterilização. Concluiu-se que 35% das autoclaves analisadas não estão realizando o processo de esterilização do instrumental e que algumas falhas durante o processamento do instrumental contaminado ainda existem e deveriam ser corrigidas.The aim of this study was to evaluate the occurrence of autoclave sterilization at dental offi ces by means of biological indicators and questionnaires, as well as to know the clinical practice of processing the contaminated instruments. Three biological indicators (close to the fi lter, at the center and close to the door) were intro duced into 40 autoclaves along with instruments. Next, indicators (test and control) were incubated for 48 hours in order to check the culture medium. The test-indicators had a change in the color of the culture medium from purple to yellow in 14 (35%) of autoclaves. Most dental surgeons (DS) associate other sterilization methods, such as chemical and dry heat, with damp heat. No Dental Surgeon routinely use biological monitoring at their offi ces. From the 31 Dental Surgeons(77.5%) who use physical and/or chemical control of sterili zation, only 74.2% do it every cycle. The great majority of DS (75%) use the envelope for packing instruments. However, 77.5% of them do not write the sterilization date on the package. It was concluded that 35% of the analyzed autoclaves did not perform the instrument sterilization process and that some flaws during processing of the contaminated instruments still occur and should be corrected

Original research Microbiology Tiago André Fontoura de MELO (a)

Are bovine teeth a suitable substitute for human teeth in in vitro studies to assess endotoxin load in root canals? Abstract: The present study aimed to determine the feasibility of using bovine teeth as a suitable alternative for human teeth, in experiments involving in vitro endotoxin contamination. Twenty bovine central incisors and 20 human single-root premolars had their dental crowns removed and root lengths set at 16 mm. Root canals were prepared up to #60 K-file size and sterilized with cobalt-60 gamma irradiation (20 kGy, 6 h). The teeth were randomly divided into four groups: G1-bovine teeth (bovine negative control, n = 10), G2-human teeth (human negative control, n = 10), G3-bovine teeth, inoculated with Escherichia coli (055:B55) LPS, and G4-human teeth inoculated with E. coli LPS. The G1 and G2 groups were exposed to apyrogenic water. After the teeth had been incubated at 37 °C and atmospheric humidity for 24 h, the samples of solutions in the main canals were collected with apyrogenic absorbent paper tips. LPS levels were quantified using Limulus Amebocyte Lysate assay. The data obtained were statistically analyzed using one-way ANOVA, with a significance level of 5%. A high amount of endotoxin was detected in the inoculated human teeth (G4) when compared to the sterilized teeth (G2), as well as in the inoculated bovine teeth (G3) when compared to the inoculated human teeth (G4). However, there was no statistical difference between bovine teeth before and after the E. coli endotoxin inoculation. Therefore, under the mentioned experimental conditions, the use of bovine teeth should not be a choice for laboratory research on endotoxin contamination

In vitro antibacterial activity of a silicone-based endodontic sealer and two conventional sealers

: The aim of this study was to evaluate whether the modification in the silver component is capable of providing GuttaFlow 2 with antibacterial activity against Enterococcus faecalis compared with epoxy resin-based (AH Plus) and zinc oxide and eugenol-based (Endofill) sealers. The antibacterial activity was evaluated using a reference strain of E. faecalis (ATCC 29212). Freshly mixed sealers were subjected to the agar diffusion test (ADT), while the direct contact test (DCT) was performed after materials setting. ADT results were obtained through measurements, in millimeters, of the inhibition zones promoted by the materials, using a digital caliper. In DCT, values of CFU/mL promoted by the three sealers were compared in three experimental periods (1 min, 1 h, and 24 h). The data were analyzed using Kruskal-Wallis and Dunn post-hoc tests (p < 0.05). In both ADT and DCT, GuttaFlow 2 presented no effect against E. faecalis, while Endofill and AH Plus showed similar inhibition zones. Endofill was the only material capable of reducing bacterial growth in DCT. In conclusion, modifications in the silver particle of GuttaFlow 2 did not result in a sealer with antibacterial effect against E. faecalis

An in vivo radiographic evaluation of the accuracy of Apex and iPex electronic Apex locators

The aim of this study was to evaluate in vivo the clinical applicability of two electronic apex locators (EALs) - Apex (Septodont) and iPex (NSK) - in different groups of human teeth by using radiography. The working lengths (WLs) of 100 root canals were determined electronically. The EAL to be used first was chosen randomly and a K-file was inserted into the root canal until the EAL display indicated the location of the apical constriction (0 mm). The K-file was fixed to the tooth and a periapical radiograph was taken using a radiographic film holder. The K-file was removed and the WL was measured. The same procedure was repeated using the other EAL. Radiographs were examined with the aid of a light-box with lens of ×4 magnification by two blinded experienced endodontists. The distance between the file tip and the root apex was recorded as follows: (A) +1 to 0 mm, (B) -0.1 to 0.5 mm, (C) -0.6 to 1 mm, (D) -1.1 to 1.5 mm, and (E) -1.6 mm or greater. For statistical purposes, these scores were divided into 2 subgroups according to the radiographic apex: acceptable (B, C, and D) and non-acceptable (A and E). Statistically significant differences were not found between the results of Apex and iPex in terms of acceptable and non-acceptable measurements (p>0.05) or in terms of the distance recorded from file tip and the radiographic apex (p>0.05). Apex and iPex EALs provided reliable measurements for WL determination for endodontic therapy