Submitted by Celso Magalhaes (celsomagalhaes@ufrrj.br) on 2022-10-18T12:51:23Z No. of bitstreams: 1 2020 - Debora Baptista Pereira.pdf: 2191500 bytes, checksum: ba51deb9e480726e604fe5f7fc5aa8cb (MD5) Made available in DSpace on 2022-10-18T12:51:24Z (GMT). No. of bitstreams: 1 2020 - Debora Baptista Pereira.pdf: 2191500 bytes, checksum: ba51deb9e480726e604fe5f7fc5aa8cb (MD5) Previous issue date: 2020-02-18 CAPES - Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior Damage to cartilaginous and bone tissue is caused by several factors such as trauma, inflammation and aging and can lead to tissue loss with functional impairment. Because it is a fabric that has low or even no regenerative capacity, treatment and recovery is difficult. In an attempt to overcome these problems, researchers have developed and perfected different regenerative techniques based on the use of polymeric biomaterials. Along with these, it is of interest to use a drug with beneficial properties to assist the treatment of cartilage areas damaged by the wear and tear caused by inflammation and injury. Atorvastatin (ATV), a cholesterol-lowering statin, has shown interesting secondary actions in several studies, such as bone anabolism due to its prolonged use. However, high doses of this input are necessary for this purpose and the commercialized forms of this drug are tablets for oral use, with little direction for cartilage and bone tissue. Thus, the objective of the work was to develop and evaluate polymeric films for controlled release of atorvastatin. In this context, films composed of polycaprolactone (PCL), a biodegradable synthetic polymer containing ATV, were developed. The films were produced using the solvent casting technique using two different methodologies? without and with drug solubilization (methods 1 and 2 respectively) and with different drug / polymer proportions. These were characterized by scanning electron microscopy (SEM), SEM coupled to dispersive energy spectroscopy (EDS), X-ray diffraction (DRX), Fourier transform infrared spectrometry (FTIR), thermogravimetric analysis (TGA) and differential scanning calorimetry. (DSC). According to the results obtained by these techniques, it was possible to conclude that the films produced by method 2 were considered better because they present greater homogeneity in the dispersion of the drug. The release of the drug present in the best films was evaluated in a phosphate buffer solution (pH 7.4) at 37 ? C and rotation of 75 rpm in a dissolver with fiber optic sensors, recording the release at predefined times for 5 days. Through this test it was demonstrated that it was released in the studied time in a prolonged way, and that both the material morphology and the diffusion process have an influence on the release mechanism, suggesting that the material on the surface is released first and then, the film is eroded, making the drug available. The degradation of the films was observed through the SEM performed after the release, proving the erosion process. Therefore, the developed films have potential application for controlled release of drugs, and may in the future be used as a biomaterial for the regeneration of cartilage tissue Danos ao tecido cartilaginoso e ?sseo s?o causados por diversos fatores como traumas, inflama??es e envelhecimento e podem acarretar na perda tecidual com comprometimento funcional. Por ser um tecido que apresenta baixa ou at? mesmo nenhuma capacidade regenerativa, se torna dif?cil o tratamento e recupera??o. Na tentativa de superar estes problemas, pesquisadores t?m desenvolvido e aperfei?oado diferentes t?cnicas regenerativas baseadas na utiliza??o de biomateriais polim?ricos. Junto a esses, ? de interesse utilizar um f?rmaco com propriedades ben?ficas para auxiliar o tratamento das ?reas cartilaginosas danificadas pelo desgaste causado por inflama??es e les?es. A atorvastatina (ATV), estatina redutora de colesterol, tem exibido em diversos estudos a??es secund?rias interessantes, como anabolismo ?sseo devido ao seu uso prolongado. Entretanto, s?o necess?rias altas doses desse insumo para esse efeito e as formas comercializadas desse f?rmaco s?o comprimidos de uso oral, tendo pouco direcionamento para o tecido cartilaginoso e ?sseo. Dessa forma, o objetivo do trabalho foi desenvolver e avaliar filmes polim?ricos para libera??o controlada de atorvastatina. Nesse contexto, foram desenvolvidos, filmes compostos por policaprolactona (PCL), um pol?mero sint?tico biodegrad?vel, contendo ATV. Os filmes foram produzidos atrav?s da t?cnica de solvent casting utilizando duas metodologias diferentes, sem e com solubiliza??o do f?rmaco (m?todos 1 e 2 respectivamente) e com diferentes propor??es f?rmaco/pol?mero. Esses foram caracterizados pelas t?cnicas de microscopia eletr?nica de varredura (MEV), MEV acoplado a espectroscopia de energia dispersiva (EDS), difra??o de raios X (DRX), espectroscopia no infravermelho com transformada de Fourier (FTIR), an?lise termogravim?trica (TGA) e calorimetria diferencial de varredura (DSC). De acordo com os resultados obtidos por essas t?cnicas, foi poss?vel concluir que os filmes produzidos pelo m?todo 2 foram considerados melhores por apresentarem maior homogeneidade na dispers?o do f?rmaco. A libera??o do f?rmaco presente nos melhores filmes foi avaliada em solu??o tamp?o fosfato (pH 7,4) a 37 0C e rota??o de 75 rpm em um dissolutor com sensores de fibra ?tica, registrando a libera??o em tempos pr?definidos por 5 dias. Atrav?s desse teste demonstrou-se que o mesmo foi liberado no tempo estudado de forma prolongada, e que tanto a morfologia do material quanto o processo de difus?o t?m influ?ncia no mecanismo de libera??o, sugerindo que o material na superf?cie ? liberado primeiro e em seguida, o filme sofre eros?o, disponibilizando o f?rmaco. A degrada??o dos filmes foi observada atrav?s do MEV realizada ap?s a libera??o, comprovando o processo de eros?o. Portanto, os filmes desenvolvidos t?m potencial aplica??o para libera??o controlada de f?rmacos, podendo futuramente ser utilizado como biomaterial para regenera??o do tecido cartilaginoso