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1.
Infect Immun ; 87(12)2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31527130

RESUMEN

Candida-associated denture stomatitis (DS) is a persistent and chronic oral infection of the denture-bearing palatal mucosa. DS stems from the ability of the fungal opportunistic pathogen Candida albicans to adhere to denture material and invade palatal tissue. Although DS is the most prevalent form of oral candidiasis, there are currently no feasible therapeutic strategies for the prevention of this recurrent condition. We developed a peptide-based antimicrobial bioadhesive formulation specifically designed for oral topical formulation. In this study, we aimed to evaluate the applicability of the novel formulation for the prevention of C. albicans colonization on denture material and development of clinical disease. To that end, using the latest technological advances in dental digital design and three-dimensional (3D) printing, we fabricated an intraoral device for rats with universal fit. The device was successfully installed and used to develop clinical DS. Importantly, by taking a preventative therapeutic approach, we demonstrated the potential clinical utility of the novel formulation as a safe and feasible prophylactic agent against DS.


Asunto(s)
Antifúngicos/farmacología , Candida albicans/efectos de los fármacos , Candidiasis Bucal/prevención & control , Cementos Dentales/farmacología , Estomatitis Subprotética/prevención & control , Animales , Antifúngicos/química , Biopelículas/efectos de los fármacos , Biopelículas/crecimiento & desarrollo , Candida albicans/crecimiento & desarrollo , Candidiasis Bucal/tratamiento farmacológico , Candidiasis Bucal/microbiología , Cementos Dentales/química , Dentaduras/microbiología , Modelos Animales de Enfermedad , Masculino , Mucosa Bucal/microbiología , Ratas , Ratas Sprague-Dawley , Estomatitis Subprotética/tratamiento farmacológico , Estomatitis Subprotética/microbiología
2.
Nanomedicine ; 14(3): 919-927, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29408655

RESUMEN

Maintaining the vitality of the dental pulp, the highly innervated and highly vascular, innermost layer of the tooth, is a critical goal of any dental procedure. Upon injury, targeting the pulp with specific therapies is challenging because it is encased in hard tissues. This project describes a method that can effectively deliver therapeutic agents to the pulp. This method relies on the use of nanoparticles that can be actively steered using magnetic forces to the pulp, traveling through naturally occurring channels in the dentin (the middle layer of the tooth). This method can reduce the inflammation of injured pulp and improve the penetration of dental adhesives into dentin. Such a delivery method would be less expensive, and both less painful and less traumatic than existing therapeutic options available for treatment of injured dental pulp. This technique would be simple and could be readily translated to clinical use.


Asunto(s)
Antiinflamatorios/administración & dosificación , Pulpa Dental/efectos de los fármacos , Sistemas de Liberación de Medicamentos , Inflamación/tratamiento farmacológico , Nanopartículas de Magnetita/administración & dosificación , Prednisolona/administración & dosificación , Enfermedades Estomatognáticas/tratamiento farmacológico , Animales , Antiinflamatorios/química , Femenino , Nanopartículas de Magnetita/química , Masculino , Prednisolona/química , Ratas , Ratas Long-Evans
3.
Dent Mater ; 34(9): 1310-1322, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-29935766

RESUMEN

OBJECTIVES: A nanoparticle-doped adhesive that can be controlled with magnetic forces was recently developed to deliver drugs to the pulp and improve adhesive penetration into dentin. However, it did not have bactericidal and remineralization abilities. The objectives of this study were to: (1) develop a magnetic nanoparticle-containing adhesive with dimethylaminohexadecyl methacrylate (DMAHDM), amorphous calcium phosphate nanoparticles (NACP) and magnetic nanoparticles (MNP); and (2) investigate the effects on dentin bond strength, calcium (Ca) and phosphate (P) ion release and anti-biofilm properties. METHODS: MNP, DMAHDM and NACP were mixed into Scotchbond SBMP at 2%, 5% and 20% by mass, respectively. Two types of magnetic nanoparticles were used: acrylate-functionalized iron nanoparticles (AINPs); and iron oxide nanoparticles (IONPs). Each type was added into the resin at 1% by mass. Dentin bonding was performed with a magnetic force application for 3min, provided by a commercial cube-shaped magnet. Dentin shear bond strengths were measured. Streptococcus mutans biofilms were grown on resins, and metabolic activity, lactic acid and colony-forming units (CFU) were determined. Ca and P ion concentrations in, and pH of biofilm culture medium were measured. RESULTS: Magnetic nanoparticle-containing adhesive using magnetic force increased the dentin shear bond strength by 59% over SBMP Control (p<0.05). Adding DMAHDM and NACP did not adversely affect the dentin bond strength (p>0.05). The adhesive with MNP+DMAHDM+NACP reduced the S. mutans biofilm CFU by 4 logs. For the adhesive with NACP, the biofilm medium became a Ca and P ion reservoir. The biofilm culture medium of the magnetic nanoparticle-containing adhesive with NACP had a safe pH of 6.9, while the biofilm medium of commercial adhesive had a cariogenic pH of 4.5. SIGNIFICANCE: Magnetic nanoparticle-containing adhesive with DMAHDM and NACP under a magnetic force yielded much greater dentin bond strength than commercial control. The novel adhesive reduced biofilm CFU by 4 logs and increased the biofilm pH from a cariogenic pH 4.5-6.9, and therefore is promising to enhance the resin-tooth bond, strengthen tooth structures, and suppress secondary caries at the restoration margins.


Asunto(s)
Antibacterianos/síntesis química , Antibacterianos/farmacología , Fosfatos de Calcio/farmacología , Recubrimientos Dentinarios/síntesis química , Recubrimientos Dentinarios/farmacología , Nanopartículas de Magnetita/química , Metacrilatos/farmacología , Remineralización Dental/métodos , Biopelículas/efectos de los fármacos , Concentración de Iones de Hidrógeno , Cementos de Resina/farmacología , Células Madre , Streptococcus mutans/efectos de los fármacos
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