Desenvolvimento e estudo de nanoemulsões para incorporação de triancinolona acetonida

Recurrent aphthous stomatitis (RAS) is the most common condition of the oral mucosa. Some local and systemic factors may be associated to the disease and there is evidence that an immunogenetic basis may be present. Disease control depends on its clinical presentation and includes immunosuppre...

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Autor principal: Silva, Sauara Marques da
Outros Autores: Silva Júnior, Arnóbio Antônio da
Formato: bachelorThesis
Idioma:pt_BR
Publicado em: Universidade Federal do Rio Grande do Norte
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Endereço do item:https://repositorio.ufrn.br/handle/123456789/50284
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Resumo:Recurrent aphthous stomatitis (RAS) is the most common condition of the oral mucosa. Some local and systemic factors may be associated to the disease and there is evidence that an immunogenetic basis may be present. Disease control depends on its clinical presentation and includes immunosuppressive drugs, topical and systemic corticosteroids, anesthetic and antimicrobial solutions. Triamcinolone acetonide (TA) is an organic compound, defined as a synthetic corticosteroid used topically for the treatment and relief of dermatopathies and oral inflammatory lesions, such as mouth ulcers. As it is a low solubility compound in aqueous medium, it’s incorporation into hydrophilic films is hampered, the nanoemulsion becomes a solution to develop a new pharmaceutical form. Therefore, it was aimed to obtain a stable nanoemulsion with TA incorporation. In this work, a prototype of TA was incorporated into nanoemulsion, the aqueous phase (FA) being composed of glycerin, soybean oil, Tween 80® and Span 80® and the oil phase (FO) being composed of polaxamer 407 (P407) and water, by phase inversion method. The characterization was carried out in terms of droplet size, polydispersity index (PDI), hydrogenion potential (pH), zeta potential and standard deviation, and these same parameters were used to evaluate the stability of the system.The incorporations of 1%, 2.5% and 5% of triamcinolone in the nanoemulsions were sustained droplet sizes < 200 nm and PDI < 0.3. However, due to the drug sedimentation during the study, new possibilities for maintaining stability were tested, with the incorporation of a cream gel being one of them. The cream gel consists of an aqueous phase, composed of a gel former, such as carbomer or hydroxyethylcellulose, and an oil phase, composed of waxes and light emollients. The gelling process contributed greatly to increase the viscosity of the samples, may contribute to prevent drug-leakage. The nanoemulsion systems incorporated with TA were successfully obtained and characterized, showcasing significant and relevant results for the development of this current formulation as an alternative treatment for aphthosis, allowing, consequently, the continuation of the study, aiming to improve it, with the development of new tests.