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1.
J Oral Rehabil ; 38(4): 253-62, 2011 Apr.
Article in English | MEDLINE | ID: mdl-20868428

ABSTRACT

The aim of this comparative clinical study was to evaluate a novel bioactive glass-ceramic (Biosilicate® 1-20 µm particles) to treat dentine hypersensitivity (DH). Volunteers (n = 120 patients/ 230 teeth) received the following treatments: G1-Sensodyne® , G2-SensiKill®, G3-Biosilicate® incorporated in a 1% water-free-gel and G4-Biosilicate® mixed with distilled water at 1:10 ratio. G1 and G3 were applied at home, daily for 30 days; G2 and G4 were applied once a week by a dentist (four applications). A visual analogue scale (VAS) was employed to evaluate pain for each quadrant in one sensitive tooth at baseline, weekly during treatment and during a 6-month follow-up period. Dentine hypersensitivity values (G1/n= 52), (G2/n =62), (G3/n = 59) and (G4/n = 59) were analysed with Kruskal-Wallis/Dunn tests. All the products were efficient in reducing DH after 4 weeks. Among the four materials tested, G4 demonstrated the best clinical performance and provided the fastest treatment to reduce DH pain. Distilled water proved to be an adequate vehicle to disperse Biosilicate®. Low DH scores were maintained during the 6-month follow-up period. The hypothesis that the novel bioactive glass-ceramic may be an efficient treatment for DH was confirmed.


Subject(s)
Biocompatible Materials/therapeutic use , Ceramics , Dentin Desensitizing Agents/therapeutic use , Dentin Sensitivity/drug therapy , Glass , Administration, Topical , Biocompatible Materials/administration & dosage , Crystallization , Dentin Desensitizing Agents/administration & dosage , Double-Blind Method , Drug Combinations , Fluorides/therapeutic use , Follow-Up Studies , Humans , Longitudinal Studies , Nitrates/therapeutic use , Pain Measurement , Phosphates/therapeutic use , Toothbrushing/methods , Toothpastes/administration & dosage , Toothpastes/therapeutic use , Treatment Outcome
2.
Drug Dev Ind Pharm ; 32(2): 229-38, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16537203

ABSTRACT

Gelatin microparticles containing propolis ethanolic extractive solution were prepared by spray-drying technique. Particles with regular morphology, mean diameter ranging of 2.27 microm to 2.48 microm, and good entrapment efficiency for propolis were obtained. The in vitro antimicrobial activity of microparticles was evaluated against microorganisms of oral importance (Enterococcus faecalis, Streptococcus salivarius, Streptococcus sanguinis, Streptococcus mitis, Streptococcus mutans, Streptococcus sobrinus, Candida albicans, and Lactobacillus casei). The utilized techniques were diffusion in agar and determination of minimum inhibitory concentration. The choice of the method to evaluate the antimicrobial activity of microparticles showed be very important. The microparticles displayed activity against all tested strains of similar way to the propolis, showing greater activity against the strains of E. salivarius, S. sanguinis, S. mitis, and C. albicans.


Subject(s)
Anti-Infective Agents/administration & dosage , Anti-Infective Agents/therapeutic use , Gelatin/chemistry , Propolis/administration & dosage , Propolis/therapeutic use , Candida albicans/drug effects , Drug Carriers , Ethanol/chemistry , Lacticaseibacillus casei/drug effects , Microbial Sensitivity Tests , Particle Size , Streptococcaceae/drug effects
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