Micropart?culas contendo nanopart?culas de quitosana usando sulfato e genipina para libera??o modificada da triancinolona: obten??o, caracteriza??o e estudo em c?lulas tumorais

• Main Author: Fons?ca, Gabriela Diniz
• Other Authors: 00840406452
• Language: Portuguese
• Published: Universidade Federal do Rio Grande do Norte 2016
• Subjects: CNPQ::CIENCIAS DA SAUDE::FARMACIA; Sistemas particulados; Quitosana; Genipina; Triancinolona; Antitumoral
• Online Access: http://repositorio.ufrn.br/handle/123456789/20305

Submitted by Automa??o e Estat?stica ([e-mail]) on 2016-04-25T22:57:38Z No. of bitstreams: 1 GabrielaDinizFonseca_DISSERT.pdf: 1765873 bytes, checksum: 5a2297e7f8e6f38144397041114ffaff (MD5) === Approved for entry into archive by Arlan Eloi Leite Silva ([e-mail]) on 2016-04-27T23:04:29Z (GMT) No. of bitstreams: 1 GabrielaDinizFonseca_DISSERT.pdf: 1765873 bytes, checksum: 5a2297e7f8e6f38144397041114ffaff (MD5) === Made available in DSpace on 2016-04-27T23:04:29Z (GMT). No. of bitstreams: 1 GabrielaDinizFonseca_DISSERT.pdf: 1765873 bytes, checksum: 5a2297e7f8e6f38144397041114ffaff (MD5) Previous issue date: 2015-03-31 === Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior (CAPES) === Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico (CNPq) === A quitosana ? um co-pol?mero biocompat?vel e biodegrad?vel amplamente usado em sistemas de libera??o de f?rmacos. A co-reticula??o da quitosana com sulfato de s?dio e genipina para forma??o de sistemas particulados ? capaz de tornar estes mais resistentes ao pH ?cido e modificar a cin?tica de libera??o de f?rmacos para a via oral. A triancinolona ? um glicocortic?ide de ampla aplica??o terap?utica por suas a??es antiinflamat?ria e imunossupressora. Os sistemas particulados foram preparados por co-reticula??o e caracterizadas quanto ao tamanho de part?cula, PDI, potencial zeta, grau de reticula??o, taxa de encapsula??o, MEV, espectroscopia de infravermelho, an?lise t?rmica, cin?tica de libera??o e estudo em c?lulas tumorais. Inicialmente foram preparadas nanopart?culas com sulfato de s?dio, sem genipina, contendo triancinolona, avaliando a propor??o do volume das fases f?rmaco/pol?mero, concentra??o de sulfato de s?dio e polissorbato 80, tempo e modo de imers?o das fases. O sistema definido para a reticula??o com a genipina apresentou tamanho de 312,20 ? 5,70 nm, PDI 0,342 ? 0,013 e potencial zeta 20,18 ? 2,28 mV. A genipina foi introduzida no sistema em diferentes concentra??es (0,5; 1,0 e 2,0 mM) e tempos de reticula??o (3, 6, 12 e 24 h). Na an?lise do tempo de reticula??o com genipina 0,5 mM, os sistemas obtiveram tamanho de 235,1 a 334,4 nm, PDI de 0,321 a 0,392 e potencial zeta de 20,92 a 30,39 mV, com grau de reticula??o que variou de 14 a 30 %. As nanopart?culas sem genipina, 6 h e 24 h de reticula??o foram escolhidas para a secagem por spray-drying, formando micropart?culas de nanopart?culas. A an?lise por micrografia eletr?nica de varredura revelou que as micropart?culas apresentaram morfologia esf?rica. A taxa de encapsula??o foi de 75 ? 2,3% usando metodologia CLAE validada. A caracteriza??o dos sistemas por infravermelho evidenciou as intera??es entre os componentes da formula??o. A an?lise t?rmica mostrou que os sistemas com maior grau de reticula??o, apresentaram uma maior estabilidade t?rmica. Na cin?tica de libera??o, o aumento do grau de reticula??o foi capaz de diminuir a velocidade de libera??o da triancinolona. Nos estudos com c?lulas HepG2 e HT-29 os sistemas microparticulados contendo triancinolona e genipina com tempo de reticula??o de 24 h apresentaram um potencial para atividade antitumoral nas c?lulas de linhagem hep?ticas HepG2. Com isso, um novo sistema de libera??o a base de quitosana obtido por co-reticula??o com sulfato de s?dio e genipina contendo triancinolona foi obtido com potencial antitumoral hep?tico. === Chitosan is a polymer biocompatibility and biodegradability widely used in drug delivery systems. The co-crosslinking of chitosan with sodium sulfate and genipin, to form particulate systems is related of making them more resistant to acidic pH and to modulate the release kinetics for the oral route. Triamcinolone is a glucocorticoid with anti-inflammatory and immunosuppressive actions. The nanoparticles were prepared by co-crosslinking and characterized for particle size, PDI, zeta potential, crosslinking degree, encapsulation rate, morphology, infrared spectroscopy, thermal analysis, release kinetics and cells studies. The nanoparticles were prepared initially without genipin with sodium sulphate and the particles parameters were monitored in function of different ratio of drug / polymer, different concentrations of sodium sulfate and polysorbate 80 and the drip mode of crosslinkers on polymers. After optimizing conditions, the chosen system parameters without genipin included mean diameter of 312.20 ? 5.70 nm, PDI 0.342 ? 0.013 and zeta potential of 20.18 ? 2.28 mV. The genipin was introduced into the system analyzing different concentrations (0.5, 1.0 and 2.0 mM) and crosslinking times (3, 6, 12 and 24 h). Evaluating crosslinking time with genipin (0.5 mM) it was showed that varying the genipin reaction time the systems size ranged from 235.1 to 334.4 nm, the PDI from 0.321 to 0.392 and zeta potential 20.92 to 30.39 mV. The crosslinking degree that coud vary from 14 to 30 %. Nanoparticles without genipina, 6 h and 24 h crosslinking time were dried by spray-drying method. Analysis by scanning electron micrograph (SEM) revealed that the microparticles showed spherical morphology. The encapsulation rate was 75 ? 2.3 % using validated HPLC methodology. The infrared analysis showed chemical interactions between the components of the formulation. Thermal analysis showed that systems with a higher degree of crosslinking had a higher thermal stability. On release kinetics, increasing the degree of crosslinking was able to decrease the concentration and rate of release of triamcinolone. In studies with liver cancer cells (HepG2) and colon (HT-29), the microparticulate prepared with triamcinolone and 24 h of crosslinking with genipin showed a potential for antitumor activity in hepatic cell line HepG2. Therefore, a new delivery system for triamcinolone on polymeric nanoparticles of chitosan cocrosslinked with genipin and sodium sulfate was obtained with hepatic antitumor potential.