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1.
J Prosthet Dent ; 112(6): 1349-55, 2014 Dec.
Article de Anglais | MEDLINE | ID: mdl-25258264

RÉSUMÉ

STATEMENT OF PROBLEM: Candida biofilms on denture surfaces are substantially reduced after a single immersion in denture cleanser. However, whether this effect is maintained when dentures are immersed in cleanser daily is unclear. PURPOSE: The purpose of this study was to evaluate the effect of the daily use of enzymatic cleanser on Candida albicans biofilms on denture base materials. MATERIAL AND METHODS: The surfaces of polyamide and poly(methyl methacrylate) resin specimens (n=54) were standardized and divided into 12 groups (n=9 per group), according to study factors (material type, treatment type, and periods of treatment). Candida albicans biofilms were allowed to form over 72 hours, after which the specimens were treated with enzymatic cleanser once daily for 1, 4, or 7 days. Thereafter, residual biofilm was ultrasonically removed and analyzed for viable cells (colony forming units/mm(2)) and enzymatic activity (phospholipase, aspartyl-protease, and hemolysin). Factors that interfered with the response variables were analyzed by 3-way ANOVA with the Holm-Sidak multiple comparison method (α=.05). RESULTS: Polyamide resin presented more viable cells of Candida albicans (P<.001) for both the evaluated treatment types and periods. Although enzymatic cleansing significantly (P<.001) reduced viable cells, daily use did not maintain this reduction (P<.001). Phospholipase activity significantly increased with time (P<.001) for both materials and treatments. However, poly(methyl methacrylate) based resin (P<.001) and enzymatic cleansing treatment (P<.001) contributed to lower phospholipase activity. Aspartyl-protease and hemolysin activities were not influenced by study factors (P>.05). CONCLUSIONS: Although daily use of an enzymatic cleanser reduced the number of viable cells and phospholipase activity, this treatment was not effective against residual biofilm over time.


Sujet(s)
Biofilms/effets des médicaments et des substances chimiques , Candida albicans/effets des médicaments et des substances chimiques , Matériaux dentaires/composition chimique , Produits de nettoyage pour appareils de prothèse dentaire/usage thérapeutique , Nylons/composition chimique , Poly(méthacrylate de méthyle)/composition chimique , Aspartic acid proteases/analyse , Borates/usage thérapeutique , Candida albicans/enzymologie , Numération de colonies microbiennes , Pellicule salivaire/microbiologie , Hémolysines/analyse , Humains , Immersion , Test de matériaux , Viabilité microbienne/effets des médicaments et des substances chimiques , Microscopie électronique à balayage , Phospholipases/analyse , Méthode en simple aveugle , Sulfates/usage thérapeutique , Propriétés de surface , Facteurs temps
2.
J Contemp Dent Pract ; 15(2): 186-9, 2014 Mar 01.
Article de Anglais | MEDLINE | ID: mdl-25095841

RÉSUMÉ

AIM: The aim of this study was to evaluate the fracture resistance of teeth submitted to several internal bleaching protocols using 35% hydrogen peroxide (35HP), 37% carbamide peroxide (37CP), 15% hydrogen peroxide with titanium dioxide nanoparticles (15HPTiO2) photoactivated by LED-laser or sodium perborate (SP). MATERIALS AND METHODS: After endodontic treatment, fifty bovine extracted teeth were divided into five groups (n = 10): G1-unbleached; G2-35HP; G3-37CP; G4-15HPTiO2 photoactivated by LED-laser and G5-SP. In the G2 and G4, the bleaching protocol was applied in 4 sessions, with 7 days intervals between each session. In the G3 and G5, the materials were kept in the pulp teeth for 21 days, but replaced every 7 days. After 21 days, the teeth were subjected to compressive load at a cross head speed of 0.5 mm/min, applied at 135° to the long axis of the root using an eletromechanical testing machine, until teeth fracture. The data were submitted to ANOVA and Tukey tests (α = 5%). RESULTS: The 35HP, 37CP, 15HPTiO2 and SP showed similar fracture resistance teeth reduction (p > 0.05). All bleaching treatments reduced the fracture resistance compared to unbleached teeth (p < 0.05). CONCLUSION: All bleaching protocols reduced the fracture resistance of endodontically-treated teeth, but there were no differences between each other. CLINICAL SIGNIFICANCE: There are several internal bleaching protocols using hydrogen peroxide in different concentrations and activation methods. This study evaluated its effects on fracture resistance in endodontically-treated teeth.


Sujet(s)
Cavité pulpaire de la dent/effets des médicaments et des substances chimiques , Agents de blanchiment des dents/usage thérapeutique , Blanchiment dentaire/méthodes , Fractures dentaires/physiopathologie , Animaux , Borates/usage thérapeutique , Peroxyde d'urée , Bovins , Analyse du stress dentaire/instrumentation , Peroxyde d'hydrogène/usage thérapeutique , Photothérapie de faible intensité , Test de matériaux , Nanoparticules , Peroxydes/usage thérapeutique , Photosensibilisants/usage thérapeutique , Répartition aléatoire , Traitement de canal radiculaire/méthodes , Contrainte mécanique , Facteurs temps , Titane/usage thérapeutique , Urée/analogues et dérivés , Urée/usage thérapeutique
3.
Int Endod J ; 46(1): 40-6, 2013 Jan.
Article de Anglais | MEDLINE | ID: mdl-22788541

RÉSUMÉ

AIM: To evaluate the effectiveness of ultrasonic activation of bleaching agents during ex vivo internal bleaching. METHODOLOGY: Fifty canine human teeth were artificially stained, root filled and divided into five groups (n = 10) that received SP - sodium perborate plus deionized water (control group), CP - 37% carbamide peroxide gel, CPUS - 37% carbamide peroxide gel plus ultrasonic application, HP - 35% hydrogen peroxide gel or HPUS - 35% hydrogen peroxide gel plus ultrasonic application. In groups CP and HP, the bleaching agent was left inside the pulp chamber for three applications of 10 min. In groups CPUS and HPUS, the same process was performed, but ultrasonic vibration was applied to the bleaching agent by an alloy tip for 30 s, with 30 s intervals. Two sessions were performed. The colour was measured initially and after each session by an intraoral dental spectrophotometer. The variation (Δ) of the colour parameters based on the CIELab system L*, a* and b*, and the colour alteration ΔE* were calculated after first and second section. Data were analysed by one-way anova and Tukey's test. RESULTS: There was no significant difference amongst groups for ΔL*, Δa* and ΔE*, but there was a significant difference for Δb* in the first and second sessions (P = 0.0006 and 0.0016, respectively). After the first session, Δb* was significantly greater for groups HP and HPUS, without a significant difference between them. For the second session, group HPUS had the greatest Δb* values, but they were similar to groups HP and SP; group CP had the lowest values, which were similar to groups CPUS and SP. CONCLUSION: Ultrasonic activation of bleaching agents during ex vivo internal bleaching was no more effective than conventional internal bleaching procedures, without activation.


Sujet(s)
Canine/effets des médicaments et des substances chimiques , Sonication , Agents de blanchiment des dents/usage thérapeutique , Blanchiment dentaire/méthodes , Borates/usage thérapeutique , Peroxyde d'urée , Couleur , Canine/anatomopathologie , Cavité pulpaire de la dent/effets des médicaments et des substances chimiques , Humains , Peroxyde d'hydrogène/usage thérapeutique , Test de matériaux , Peroxydes/usage thérapeutique , Salive artificielle/composition chimique , Spectrophotométrie/méthodes , Facteurs temps , Dyschromie dentaire/traitement médicamenteux , Urée/analogues et dérivés , Urée/usage thérapeutique , Vibration/usage thérapeutique
4.
Article de Anglais | MEDLINE | ID: mdl-21458323

RÉSUMÉ

OBJECTIVE: This article discusses the relationship between apical limit of root canal filling and success on endodontic treatment of a mandibular molar. STUDY DESIGN: A mandibular right first molar with vital pulp was endodontically treated, and 3 years later periapical lesions on mesial and distal roots were detected. The canals were retreated and obturated to the same levels as in the previous treatment. RESULTS: An 8-year radiographic follow-up showed repair of the periapical lesions on both roots. CONCLUSIONS: Results suggest that the apical limit of obturation seems to have no influence in the repair of periapical tissues in mandibular molars.


Sujet(s)
Cavité pulpaire de la dent/anatomopathologie , Molaire/anatomopathologie , Produits d'obturation des canaux radiculaires/usage thérapeutique , Apex de la racine de la dent/anatomopathologie , Adulte , Sulfate de baryum/usage thérapeutique , Bismuth/usage thérapeutique , Borates/usage thérapeutique , Association médicamenteuse , Eugénol/usage thérapeutique , Études de suivi , Gutta-percha/usage thérapeutique , Humains , Mâle , Mandibule , Maladies périapicales/imagerie diagnostique , Radiographie , Résines synthétiques/usage thérapeutique , Reprise du traitement , Obturation de canal radiculaire/méthodes , Préparation de canal radiculaire/méthodes , Dent dévitalisée/thérapie , Résultat thérapeutique , Cicatrisation de plaie , Oxyde de zinc/usage thérapeutique
5.
Gerodontology ; 28(2): 134-9, 2011 Jun.
Article de Anglais | MEDLINE | ID: mdl-19780843

RÉSUMÉ

OBJECTIVE: To determine the effectiveness of a denture cleanser in reducing the concentration of volatile sulphur compounds (VSC) and its antimicrobial action. BACKGROUND: Micro-organisms from the denture biofilm can cause local and systemic disease and halitosis. Denture cleansers are important adjuncts in oral care, but there is limited investigation on their effect in malodour compounds. MATERIAL AND METHODS: Nineteen institutionalised elderly who wore at least an upper denture were selected; their VSC concentrations were measured and the denture biofilm was collected. In phase 1, the subjects wore their old denture and data were collected before (B0) and after 7(A1), 14(A2), 28(A3) days of continuous daily use of the denture cleanser. In phase 2, new dentures were inserted and measurements were made at 30(A1.1), 60(A2.2), 90(A3.3) days of treatment. RESULTS: The VSC concentration increased from B0 to A1 (p<0.05), but no differences were found for the others intervals of times. Total micro-organism data did not show a statistical difference between times in Phase I, but in Phase II, there was a statistical difference (p<0.05) and a progressive re-colonisation was observed. CONCLUSION: Within the limits of this study, it was concluded that the denture cleanser had no antimicrobial effect and VSC levels were not reduced.


Sujet(s)
Biofilms/effets des médicaments et des substances chimiques , Produits de nettoyage pour appareils de prothèse dentaire/usage thérapeutique , Appareils de prothèse dentaire , Halitose/prévention et contrôle , Institutionnalisation , Composés du soufre/analyse , Sujet âgé , Sujet âgé de 80 ans ou plus , Bactéries/croissance et développement , Charge bactérienne , Borates/usage thérapeutique , Prothèse dentaire complète supérieure/microbiologie , Femelle , Études de suivi , Humains , Soins de longue durée , Mâle , Adulte d'âge moyen
6.
J Appl Oral Sci ; 18(3): 291-6, 2010.
Article de Anglais | MEDLINE | ID: mdl-20857010

RÉSUMÉ

OBJECTIVE: Effective cleaning of dentures is important for the maintenance of good oral hygiene for denture stomatitis patients. The in vivo efficacy of three different brands of alkaline peroxide tablets (Polident, Efferdent, and Fittydent) and two mouthwashes (CloSYS II and Corsodyl) to eliminate Candida albicans on dentures was evaluated in this in vivo study. MATERIAL AND METHODS: Ninety denture wearers with clinical evidence of denture stomatitis were randomly divided into 5 test groups and 1 control group. Each group was further divided into three subgroups in which the dentures were subjected to 15-, 30-, and 60-min disinfection procedures. The dentures of each test group were treated with one of the cleaners, while those of the control group were treated with distilled water. Swab samples from the palatal surfaces (2 cm x 2 cm template delimited area) of the upper dentures were obtained before and after 15, 30, and 60 min periods of cleaner use and examined mycologically. RESULTS: The reduction in the number of colony-forming units (CFU) of C. albicans before, and after 15, 30, and 60 min of use of CloSYS II and Corsodyl was significantly greater than that of the control group (p<0.05). Moreover, there was no statistically significant difference (p>0.05) among Polident, Efferdent and the control group in any of the treatment periods. Dentures treated with Fittydent appeared to have a significantly greater reduction in the number of Candida spp. only after 60 min of treatment. CONCLUSIONS: The results of this study showed that the use of mouthwashes significantly reduced the number of microorganisms on dentures.


Sujet(s)
Anti-infectieux locaux/usage thérapeutique , Candida albicans/effets des médicaments et des substances chimiques , Candidose buccale/traitement médicamenteux , Produits de nettoyage pour appareils de prothèse dentaire/usage thérapeutique , Bains de bouche/usage thérapeutique , Peroxydes/usage thérapeutique , Stomatite prothétique/microbiologie , Sujet âgé , Borates/usage thérapeutique , Chlorhexidine/analogues et dérivés , Chlorhexidine/usage thérapeutique , Numération de colonies microbiennes , Prothèse dentaire complète supérieure/microbiologie , Femelle , Humains , Mâle , Adulte d'âge moyen , Sulfates/usage thérapeutique , Comprimés , Facteurs temps , Résultat thérapeutique
7.
J. appl. oral sci ; J. appl. oral sci;18(3): 291-296, May-June 2010. ilus, tab
Article de Anglais | LILACS | ID: lil-557096

RÉSUMÉ

OBJECTIVE: Effective cleaning of dentures is important for the maintenance of good oral hygiene for denture stomatitis patients. The in vivo efficacy of three different brands of alkaline peroxide tablets (Polident, Efferdent, and Fittydent) and two mouthwashes (CloSYS II and Corsodyl) to eliminate Candida albicans on dentures was evaluated in this in vivo study. MATERIAL AND METHODS: Ninety denture wearers with clinical evidence of denture stomatitis were randomly divided into 5 test groups and 1 control group. Each group was further divided into three subgroups in which the dentures were subjected to 15-, 30-, and 60-min disinfection procedures. The dentures of each test group were treated with one of the cleaners, while those of the control group were treated with distilled water. Swab samples from the palatal surfaces (2 cm x 2 cm template delimited area) of the upper dentures were obtained before and after 15, 30, and 60 min periods of cleaner use and examined mycologically. RESULTS: The reduction in the number of colony-forming units (CFU) of C. albicans before, and after 15, 30, and 60 min of use of CloSYS II and Corsodyl was significantly greater than that of the control group (p<0.05). Moreover, there was no statistically significant difference (p>0.05) among Polident, Efferdent and the control group in any of the treatment periods. Dentures treated with Fittydent appeared to have a significantly greater reduction in the number of Candida spp. only after 60 min of treatment. CONCLUSIONS: The results of this study showed that the use of mouthwashes significantly reduced the number of microorganisms on dentures.


Sujet(s)
Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Anti-infectieux locaux/usage thérapeutique , Candida albicans/effets des médicaments et des substances chimiques , Candidose buccale/traitement médicamenteux , Produits de nettoyage pour appareils de prothèse dentaire/usage thérapeutique , Bains de bouche/usage thérapeutique , Peroxydes/usage thérapeutique , Stomatite prothétique/microbiologie , Borates/usage thérapeutique , Numération de colonies microbiennes , Chlorhexidine/analogues et dérivés , Chlorhexidine/usage thérapeutique , Prothèse dentaire complète supérieure/microbiologie , Sulfates/usage thérapeutique , Comprimés , Facteurs temps , Résultat thérapeutique
8.
Article de Anglais | MEDLINE | ID: mdl-19071038

RÉSUMÉ

OBJECTIVE: The aim was to evaluate the bleaching efficacy of sodium perborate/37% carbamide peroxide paste and traditional sodium perborate/distilled water for intracoronal bleaching. STUDY DESIGN: Thirty patients with dark anterior teeth were divided into 2 groups (n = 15): group A: sodium perborate/distilled water; and group B: sodium perborate/37% carbamide peroxide paste. The bleaching treatment limited each patient to the maximum of 4 changes of the bleaching agent. Initial and final color shades were measured using the Vita Lumin shade guide. RESULTS: Data was analyzed with Wilcoxon test for initial and final comparison according to the bleaching agent, demonstrating efficacy of the bleaching treatment with both agents. Mann-Whitney test was used for comparison of the efficacy of the bleaching agents, showing that there was no significant difference between them. CONCLUSION: The sodium perborate/37% carbamide peroxide association for intracoronal bleaching has proven to be as effective as sodium perborate/distilled water.


Sujet(s)
Borates/usage thérapeutique , Oxydants/usage thérapeutique , Peroxydes/usage thérapeutique , Blanchiment dentaire/méthodes , Dent dévitalisée , Urée/analogues et dérivés , Adolescent , Adulte , Peroxyde d'urée , Méthode en double aveugle , Association médicamenteuse , Femelle , Gels , Humains , Mâle , Adulte d'âge moyen , Statistique non paramétrique , Urée/usage thérapeutique , Eau , Jeune adulte
9.
Int Endod J ; 41(6): 485-92, 2008 Jun.
Article de Anglais | MEDLINE | ID: mdl-18422585

RÉSUMÉ

AIM: To evaluate ex vivo effectiveness of the three formulations of bleaching materials for intracoronal bleaching of root filled teeth using the walking bleach technique. METHODOLOGY: Extracted premolar teeth were stained artificially with human blood. After biomechanical preparation, the root canals were filled and a 3-mm thick intermediate base of zinc phosphate cement was placed at the level of the cementoenamel junction. The teeth were divided into four groups (n = 12): C (control, without bleaching material), A1 (sodium perborate + distilled water), A2 (sodium perborate + 10% carbamide peroxide) and A3 (sodium perborate + 35% carbamide peroxide). The bleaching materials were changed at 7 and 14 days. Evaluation of shade was undertaken with aid of the VITA Easyshadetrade mark (DeltaE*ab) and was performed after tooth staining and at 7, 14 and 21 days after bleaching, based on the CIELAB system. Data were analysed by anova for repeated measurements, Tukey and Dunnett tests (alpha = 0.05). RESULTS: The Tukey test revealed that group A1 (10.58 +/- 4.83 DeltaE*ab) was statistically different from the others (A2, 19.57 +/- 4.72 DeltaE*ab and A3, 17.58 +/- 3.33 DeltaE*ab), which were not different from each other. At 7 days: A1 was significantly different from A2; at 14 and 21 days: A2 and A3 were significantly better than A1; the Dunnett test revealed that the control group was different from A1, A2 and A3 at all periods (P < 0.05). CONCLUSION: Sodium perborate associated with both 10% and 35% carbamide peroxide was more effective than when associated with distilled water.


Sujet(s)
Taches de sang , Cavité pulpaire de la dent/effets des médicaments et des substances chimiques , Peroxyde d'hydrogène , Traitement de canal radiculaire/méthodes , Blanchiment dentaire/méthodes , Dyschromie dentaire/traitement médicamenteux , Analyse de variance , Prémolaire , Borates/usage thérapeutique , Peroxyde d'urée , Perméabilité de la dentine/effets des médicaments et des substances chimiques , Association médicamenteuse , Humains , Peroxyde d'hydrogène/usage thérapeutique , Techniques in vitro , Études longitudinales , Peroxydes/usage thérapeutique , Produits d'obturation des canaux radiculaires/effets indésirables , Obturation de canal radiculaire/méthodes , Statistique non paramétrique , Facteurs temps , Dyschromie dentaire/étiologie , Dent dévitalisée/thérapie , Urée/analogues et dérivés , Urée/usage thérapeutique
10.
J Clin Pediatr Dent ; 32(1): 9-12, 2007.
Article de Anglais | MEDLINE | ID: mdl-18274463

RÉSUMÉ

Treatment of darkened teeth in children is of great importance from an esthetic-functional point of view and for the psychoemotional development of the child. The objective of the present study was to determine the in vitro efficacy of three bleaching agents for whitening of artificially stained primary teeth. Fifty anterior primary teeth were artificially stained and then divided into three experimental groups (n = 15) submitted to bleaching treatment with 35% hydrogen peroxide gel, 35% carbamide peroxide gel, and 35% carbamide peroxide gel mixed with sodium perborate powder. The control group (n = 5) was not submitted to any bleaching treatment. Color changes were evaluated with a reflectance spectrophotometer and possible alterations in the enamel surface after bleaching were measured by Vickers microhardness testing. The data were assessed using the Student's t test. The results confirmed the bleaching action of the three agents tested. No significant difference in mean microhardness was observed between the three bleaching agents when compared to the control group.


Sujet(s)
Émail dentaire/effets des médicaments et des substances chimiques , Blanchiment dentaire/méthodes , Dyschromie dentaire/traitement médicamenteux , Érosion dentaire/induit chimiquement , Dent de lait/effets des médicaments et des substances chimiques , Administration par voie topique , Borates/usage thérapeutique , Peroxyde d'urée , Association médicamenteuse , Dureté/effets des médicaments et des substances chimiques , Humains , Peroxyde d'hydrogène/usage thérapeutique , Techniques in vitro , Peroxydes/usage thérapeutique , Photochimie , Spectrophotométrie , Érosion dentaire/prévention et contrôle , Dent de lait/physiopathologie , Urée/analogues et dérivés , Urée/usage thérapeutique
11.
Dent Traumatol ; 19(6): 309-13, 2003 Dec.
Article de Anglais | MEDLINE | ID: mdl-15022998

RÉSUMÉ

Discoloration of non-vital teeth is an esthetic deficiency frequently requiring bleaching treatment. The purpose of this study was to evaluate in vitro the cervical base efficacy in order to prevent or to minimize the leakage along the root canal filling and into the dentinal tubules. Thirty-eight extracted single-root human teeth were used, which were biomechanically prepared, filled, and divided into three experimental groups: G1, a cervical base was applied (3 mm of thickness) below the cemento-enamel junction, with resin-modified glass-ionomer cement (Vitremer); G2, the base was done with glass-ionomer cement (Vidrion R); and G3 (Control), did not receive any material as base. A mixture of sodium perborate and hydrogen peroxide 30% was placed inside the pulp chamber for 3 days, and the access opening was sealed with Cimpat. This procedure was repeated thrice. Soon after this, a paste of calcium hydroxide was inserted into the pulp chamber for 14 days. All teeth were covered with two layers of sticky wax, except the access opening, and immersed in blue India Ink for 5 days. The results did not show statistically significant differences between the three groups concerning the leakage inside the dentinal tubules. Regarding the apical direction, a statistical difference (ANOVA P < 0.05) was observed among the experimental group G1 and control group G3. No statistically significant difference was observed between G2 and G3 groups. Therefore, the placement of a cervical base before internal bleaching procedures is still recommended.


Sujet(s)
Percolation dentaire/prévention et contrôle , Perméabilité de la dentine/effets des médicaments et des substances chimiques , Produits d'obturation des canaux radiculaires/usage thérapeutique , Blanchiment dentaire/méthodes , Col de la dent/effets des médicaments et des substances chimiques , Dyschromie dentaire/thérapie , Analyse de variance , Borates/usage thérapeutique , Hydroxyde de calcium/usage thérapeutique , Ciments dentaires/usage thérapeutique , Cavité pulpaire de la dent/effets des médicaments et des substances chimiques , Ciment ionomère au verre/usage thérapeutique , Humains , Peroxyde d'hydrogène/usage thérapeutique , Techniques in vitro , Céments résine/usage thérapeutique , Traitement de canal radiculaire/effets indésirables , Dyschromie dentaire/étiologie , Dent dévitalisée/thérapie
12.
Int Endod J ; 34(7): 495-500, 2001 Oct.
Article de Anglais | MEDLINE | ID: mdl-11601765

RÉSUMÉ

AIM: The purpose of the present study was to evaluate microleakage of a fourth generation dentine-bonding agent and composite restoration during a walking bleach treatment. METHODOLOGY: Thirty extracted non-carious incisors were selected and conventional root canal treatment was performed. Teeth were randomly divided into 3 groups (n = 10): group A (control), access cavities were restored with a fourth generation dentine-bonding agent, and incrementally restored with composite resin; group B, a paste composed of sodium perborate and hydrogen peroxide was placed into the pulp chamber and sealed with glass ionomer cement for 7 days, teeth were then restored in the same manner as group A; group C, a paste of sodium perborate and hydrogen peroxide was placed in the pulp chamber for 7 days and then after removal of the bleaching mixture, pulp chambers were filled with a calcium hydroxide paste and cavities sealed with glass ionomer for 1 week. The cavities were then restored with bonded restorations as in groups A and B. Teeth were subjected to thermal cycling and immersed in methylene blue for 8 h. Teeth were sectioned from buccal to lingual, through the centre of the restoration, using a diamond disk. Leakage was assessed using a standard scheme, under magnification (x20). Data were submitted to statistical analysis using nonparametric Kruskal-Wallis test. RESULTS: Groups A and C exhibited similar leakage patterns, and both demonstrated less leakage values than group B (P < 0.05). CONCLUSIONS: It was concluded that bleaching with sodium perborate and hydrogen peroxide increases microleakage; short-term use of a calcium hydroxide medicament did not increase microleakage.


Sujet(s)
Hydroxyde de calcium/composition chimique , Percolation dentaire/classification , Produits d'obturation des canaux radiculaires/composition chimique , Traitement de canal radiculaire/méthodes , Blanchiment dentaire , Borates/composition chimique , Borates/usage thérapeutique , Hydroxyde de calcium/usage thérapeutique , Agents colorants , Résines composites/composition chimique , Collage dentaire , Cavité pulpaire de la dent/ultrastructure , Restaurations dentaires permanentes , Agents de collage dentinaire/composition chimique , Agents de collage dentinaire/classification , Ciment ionomère au verre/composition chimique , Humains , Peroxyde d'hydrogène/composition chimique , Peroxyde d'hydrogène/usage thérapeutique , Immersion , Bleu de méthylène , Oxydants/composition chimique , Oxydants/usage thérapeutique , Produits d'obturation des canaux radiculaires/usage thérapeutique , Statistique non paramétrique , Thermodynamique
15.
Int Endod J ; 31(2): 85-9, 1998 Mar.
Article de Anglais | MEDLINE | ID: mdl-9868933

RÉSUMÉ

Teeth with induced chronic periradicular periodontitis in dogs were root canal treated. After the biomechanical preparation, using K files and 5.25% sodium hypochlorite as the irrigant solution, all root canals were dressed with an antibacterial dressing based on calcium hydroxide, which was left in place for 7 days. After this time, the root canals were obturated with lateral condensation of cold gutta-percha with either a calcium hydroxide root canal filling material (Sealapex) or a zinc oxide-eugenol sealer (Fill Canal). After 270 days, histopathological analysis showed better apical and periapical repair in the teeth obturated with Sealapex (P < 0.05).


Sujet(s)
Sulfate de baryum/usage thérapeutique , Bismuth/usage thérapeutique , Borates/usage thérapeutique , Hydroxyde de calcium/usage thérapeutique , Eugénol/usage thérapeutique , Parodontite périapicale/traitement médicamenteux , Résines synthétiques/usage thérapeutique , Produits d'obturation des canaux radiculaires/usage thérapeutique , Salicylates/usage thérapeutique , Oxyde de zinc/usage thérapeutique , Animaux , Maladie chronique , Chiens , Association médicamenteuse
16.
Rev. argent. micol ; 21(2): 5-7, 1998. tab
Article de Espagnol | LILACS | ID: lil-235076

RÉSUMÉ

Se estudió la acción inhibidora "in vitro" de los siguientes antisépticos: etil mercurio tiosalicilato de sodio, azida sódica, borato de sodio, yoduro de potasio, fenol y cloro, frente a cultivos de 5 cepas de Prototheca wickerhamii. La acción "in vitro" de estas drogas fue medida mediante el halo de inhibición que produjeron en los cultivos de Prototheca en medio de agar-miel de Sabouraud incubados a 28ºC. Los resultados obtenidos permitieron establecer que todas las cepas eran uniformemente susceptibles al etilmercurio tiosalicilato de sodio y a la azida sódica, la mayor parte fue inhibida por el yoduro de potasio, en tanto que, el borato de sodio, el fenol y el cloro resultaron inactivos en las diluciones utilizadas


Sujet(s)
Anti-infectieux locaux , Eucaryotes/effets des médicaments et des substances chimiques , Techniques in vitro , Prototheca/effets des médicaments et des substances chimiques , Azotures/usage thérapeutique , Borates/usage thérapeutique , Chlore/usage thérapeutique , Fèces/microbiologie , Lait/microbiologie , Phénol/usage thérapeutique , Iodure de potassium/usage thérapeutique , Prototheca/isolement et purification , Prototheca/pathogénicité , Assainissement des Piscines , Thiomersal/usage thérapeutique
17.
Rev. argent. micol ; 21(2): 5-7, 1998. tab
Article de Espagnol | BINACIS | ID: bin-16152

RÉSUMÉ

Se estudió la acción inhibidora "in vitro" de los siguientes antisépticos: etil mercurio tiosalicilato de sodio, azida sódica, borato de sodio, yoduro de potasio, fenol y cloro, frente a cultivos de 5 cepas de Prototheca wickerhamii. La acción "in vitro" de estas drogas fue medida mediante el halo de inhibición que produjeron en los cultivos de Prototheca en medio de agar-miel de Sabouraud incubados a 28ºC. Los resultados obtenidos permitieron establecer que todas las cepas eran uniformemente susceptibles al etilmercurio tiosalicilato de sodio y a la azida sódica, la mayor parte fue inhibida por el yoduro de potasio, en tanto que, el borato de sodio, el f


Sujet(s)
Techniques in vitro , Prototheca/effets des médicaments et des substances chimiques , Eucaryotes/effets des médicaments et des substances chimiques , Anti-infectieux locaux , Fèces/microbiologie , Lait/microbiologie , Thiomersal/usage thérapeutique , Azotures/usage thérapeutique , Borates/usage thérapeutique , Iodure de potassium/usage thérapeutique , Chlore/usage thérapeutique , Phénol/usage thérapeutique , Prototheca/isolement et purification , Prototheca/pathogénicité , Assainissement des Piscines
18.
West Indian Med J ; 42(3): 121-3, 1993 Sep.
Article de Anglais | MEDLINE | ID: mdl-8273321

RÉSUMÉ

A randomized controlled trial of Solcoseryl, DuoDerm and conventional conservative therapy with Eusol has been performed in 32 patients with homozygous sickle-cell (SS) disease. After 12 weeks' baseline observation, patients were randomized to one of three therapies and monitored for a further 12 weeks. Of 44 ulcerated legs, 20 received control treatment, 12 Solcoseryl and 12 DuoDerm. DuoDerm was generally unacceptable, and two-thirds of the patients defaulted from this treatment. Solcoseryl increased ulcer healing compared to the controls but the difference was not significant. Solcoseryl was well tolerated and may have a role in the treatment of chronic leg ulcers of sickle-cell disease.


Sujet(s)
Actihaemyl/usage thérapeutique , Drépanocytose/complications , Colloïdes/usage thérapeutique , Ulcère de la jambe/thérapie , Pansements occlusifs , Adulte , Anti-infectieux/usage thérapeutique , Pansements hydrocolloïdaux , Borates/usage thérapeutique , Maladie chronique , Humains , Ulcère de la jambe/traitement médicamenteux , Ulcère de la jambe/étiologie , Hypochlorite de sodium/usage thérapeutique
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