Sistemas microemulsionados como carreador lipídico para fármacos insolúveis
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFRN |
Texto Completo: | https://repositorio.ufrn.br/jspui/handle/123456789/13194 |
Resumo: | Several pharmaceutical products have been developed in recent years aiming to enhance the treatment of diseases by increasing the effectiveness of drugs. Many of these new products are based on new drug delivery systems. Among these, microemulsions, which were first studied in 1943 by Hoar and Schulman, is of great interest. Microemulsion can be defined as a thermodynamically stable, isotropic, translucent and transparent system of two immiscible liquids stabilized by a surfactant film located in the oil / water interface. The aim os this work was the incorporation of Amphotericin B and Simvasatin to a microemulsion system and analyzes its physicochemical properties and their therapeutical activity when incorporated into this system. Some very promising results were achieved as the reduction of the toxicity and maintenance of the efficacy of the Amphotericin B incorpored into a microemulsion, which was demonstrated in the in vitro pharmacotoxicological study. As for the incorporation of Simvastatin in microemulsion, it was observed a significant improvement in the potential antiinflammatory and anti-infective properties when the system was use to treat infected wounds (simvastatin pleiotropic effects). Therefore, it can be concluded that the incorporation of these drugs into microemulsion system reveal the potential of microemulsions as a promising and novel dosage form, qualifying them for future trials in order to make them available in the pharmaceutical market |
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Damasceno, Bolivar Ponciano Goulart de Limahttp://lattes.cnpq.br/6407334157973308http://lattes.cnpq.br/6907806915889763Maranhão, Técia Maria de Oliveirahttp://lattes.cnpq.br/7869140767244263Pedrosa, Matheus de Freitas Fernandeshttp://lattes.cnpq.br/2929963416385218Frezard, Frederic Jean Georgeshttp://lattes.cnpq.br/1339716092644256Badaró, Roberto José da Silvahttp://lattes.cnpq.br/2172673138599748Egito, Eryvaldo Sócrates Tabosa do2014-12-17T14:13:35Z2011-02-072014-12-17T14:13:35Z2010-06-19DAMASCENO, Bolivar Ponciano Goulart de Lima. Sistemas microemulsionados como carreador lipídico para fármacos insolúveis. 2010. 202 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal do Rio Grande do Norte, Natal, 2010.https://repositorio.ufrn.br/jspui/handle/123456789/13194Several pharmaceutical products have been developed in recent years aiming to enhance the treatment of diseases by increasing the effectiveness of drugs. Many of these new products are based on new drug delivery systems. Among these, microemulsions, which were first studied in 1943 by Hoar and Schulman, is of great interest. Microemulsion can be defined as a thermodynamically stable, isotropic, translucent and transparent system of two immiscible liquids stabilized by a surfactant film located in the oil / water interface. The aim os this work was the incorporation of Amphotericin B and Simvasatin to a microemulsion system and analyzes its physicochemical properties and their therapeutical activity when incorporated into this system. Some very promising results were achieved as the reduction of the toxicity and maintenance of the efficacy of the Amphotericin B incorpored into a microemulsion, which was demonstrated in the in vitro pharmacotoxicological study. As for the incorporation of Simvastatin in microemulsion, it was observed a significant improvement in the potential antiinflammatory and anti-infective properties when the system was use to treat infected wounds (simvastatin pleiotropic effects). Therefore, it can be concluded that the incorporation of these drugs into microemulsion system reveal the potential of microemulsions as a promising and novel dosage form, qualifying them for future trials in order to make them available in the pharmaceutical marketInúmeros produtos farmacêuticos vêm sendo desenvolvidos nos últimos anos com a finalidade de incrementar o tratamento de doenças pelo aumento da eficácia de fármacos. Grande parte destes novos produtos está baseada nos novos sistemas transportadores de fármacos. Entre eles destacamse as microemulsões, que foram primeiramente estudadas em 1943 por Hoar e Schulman. Microemulsão pode ser definida como um sistema termodinamicamente estável, isotrópico, translúcido e transparente de dois líquidos imiscíveis estabilizados por um filme de tensoativos localizados na interface óleo/água. O objetivo deste trabalho foi incorporar anfotericina B e sinvastatina em um sistema microemulsionado e analisar suas propriedades físico-químicas e suas ações terapêuticas após a incorporação destes fármacos ao sistema. Alguns resultados muito promissores foram alcançados como a redução da toxicidade e a permanência da eficácia da anfotericina B incorporada em uma microemulsão durante o estudo farmacotoxicológico in vitro. Quanto à incorporação da sinvastatina na microemulsão, foi constatada uma melhora significativa no potencial antiinflamatório e antiinfeccioso (efeitos pleiotrópicos da sinvastatina) em feridas tratadas com esse sistema. Portanto, podemos concluir que a incorporação desses fármacos em sistemas microemulsionados faz das microemulsões uma nova e promissora apresentação farmacêutica, habilitando-a a futuros ensaios com a finalidade de torná-los disponíveis no mercado farmacêuticoConselho Nacional de Desenvolvimento Científico e Tecnológicoapplication/pdfporUniversidade Federal do Rio Grande do NortePrograma de Pós-Graduação em Ciências da SaúdeUFRNBRCiências da SaúdeAnfotericina BEfeitos pleiotrópicosFarmacotoxicidadeMicroemulsãoNovos sistemas transportadores de fármacosSinvastatinaAmphotericin BMicroemulsionNew drug delivery systemPharmacotoxicityPleiotropic effectssimvastatinCNPQ::CIENCIAS DA SAUDESistemas microemulsionados como carreador lipídico para fármacos insolúveisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/embargoedAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNTEXTBolivarPGLD_DISSERT.pdf.txtBolivarPGLD_DISSERT.pdf.txtExtracted texttext/plain57185https://repositorio.ufrn.br/bitstream/123456789/13194/11/BolivarPGLD_DISSERT.pdf.txte6e55badfed80f37116e1206f742b2e8MD511SistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.txtSistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.txtExtracted texttext/plain57203https://repositorio.ufrn.br/bitstream/123456789/13194/15/SistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.txt91388fc1c12bc005529e044fa20e3e6dMD515THUMBNAILBolivarPGLD_DISSERT.pdf.jpgBolivarPGLD_DISSERT.pdf.jpgIM Thumbnailimage/jpeg2027https://repositorio.ufrn.br/bitstream/123456789/13194/12/BolivarPGLD_DISSERT.pdf.jpgeaa08a1a3d7cbf12fbcc3c65b4c62893MD512SistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.jpgSistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.jpgGenerated Thumbnailimage/jpeg1250https://repositorio.ufrn.br/bitstream/123456789/13194/16/SistemasMicroemulsionadosCarreador_Damasceno_2010.pdf.jpg831b2a38b18e48422c8c462cfda75b9bMD516ORIGINALSistemasMicroemulsionadosCarreador_Damasceno_2010.pdfapplication/pdf1624811https://repositorio.ufrn.br/bitstream/123456789/13194/1/SistemasMicroemulsionadosCarreador_Damasceno_2010.pdf4e49d5598ae806bbd9ddd7c33b6e903cMD51123456789/131942020-02-07 13:28:01.081oai:https://repositorio.ufrn.br:123456789/13194Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2020-02-07T16:28:01Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.por.fl_str_mv |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
title |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
spellingShingle |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis Damasceno, Bolivar Ponciano Goulart de Lima Anfotericina B Efeitos pleiotrópicos Farmacotoxicidade Microemulsão Novos sistemas transportadores de fármacos Sinvastatina Amphotericin B Microemulsion New drug delivery system Pharmacotoxicity Pleiotropic effects simvastatin CNPQ::CIENCIAS DA SAUDE |
title_short |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
title_full |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
title_fullStr |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
title_full_unstemmed |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
title_sort |
Sistemas microemulsionados como carreador lipídico para fármacos insolúveis |
author |
Damasceno, Bolivar Ponciano Goulart de Lima |
author_facet |
Damasceno, Bolivar Ponciano Goulart de Lima |
author_role |
author |
dc.contributor.authorID.por.fl_str_mv |
|
dc.contributor.authorLattes.por.fl_str_mv |
http://lattes.cnpq.br/6407334157973308 |
dc.contributor.advisorID.por.fl_str_mv |
|
dc.contributor.advisorLattes.por.fl_str_mv |
http://lattes.cnpq.br/6907806915889763 |
dc.contributor.referees1.pt_BR.fl_str_mv |
Maranhão, Técia Maria de Oliveira |
dc.contributor.referees1ID.por.fl_str_mv |
|
dc.contributor.referees1Lattes.por.fl_str_mv |
http://lattes.cnpq.br/7869140767244263 |
dc.contributor.referees2.pt_BR.fl_str_mv |
Pedrosa, Matheus de Freitas Fernandes |
dc.contributor.referees2ID.por.fl_str_mv |
|
dc.contributor.referees2Lattes.por.fl_str_mv |
http://lattes.cnpq.br/2929963416385218 |
dc.contributor.referees3.pt_BR.fl_str_mv |
Frezard, Frederic Jean Georges |
dc.contributor.referees3ID.por.fl_str_mv |
|
dc.contributor.referees3Lattes.por.fl_str_mv |
http://lattes.cnpq.br/1339716092644256 |
dc.contributor.referees4.pt_BR.fl_str_mv |
Badaró, Roberto José da Silva |
dc.contributor.referees4ID.por.fl_str_mv |
|
dc.contributor.referees4Lattes.por.fl_str_mv |
http://lattes.cnpq.br/2172673138599748 |
dc.contributor.author.fl_str_mv |
Damasceno, Bolivar Ponciano Goulart de Lima |
dc.contributor.advisor1.fl_str_mv |
Egito, Eryvaldo Sócrates Tabosa do |
contributor_str_mv |
Egito, Eryvaldo Sócrates Tabosa do |
dc.subject.por.fl_str_mv |
Anfotericina B Efeitos pleiotrópicos Farmacotoxicidade Microemulsão Novos sistemas transportadores de fármacos Sinvastatina |
topic |
Anfotericina B Efeitos pleiotrópicos Farmacotoxicidade Microemulsão Novos sistemas transportadores de fármacos Sinvastatina Amphotericin B Microemulsion New drug delivery system Pharmacotoxicity Pleiotropic effects simvastatin CNPQ::CIENCIAS DA SAUDE |
dc.subject.eng.fl_str_mv |
Amphotericin B Microemulsion New drug delivery system Pharmacotoxicity Pleiotropic effects simvastatin |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS DA SAUDE |
description |
Several pharmaceutical products have been developed in recent years aiming to enhance the treatment of diseases by increasing the effectiveness of drugs. Many of these new products are based on new drug delivery systems. Among these, microemulsions, which were first studied in 1943 by Hoar and Schulman, is of great interest. Microemulsion can be defined as a thermodynamically stable, isotropic, translucent and transparent system of two immiscible liquids stabilized by a surfactant film located in the oil / water interface. The aim os this work was the incorporation of Amphotericin B and Simvasatin to a microemulsion system and analyzes its physicochemical properties and their therapeutical activity when incorporated into this system. Some very promising results were achieved as the reduction of the toxicity and maintenance of the efficacy of the Amphotericin B incorpored into a microemulsion, which was demonstrated in the in vitro pharmacotoxicological study. As for the incorporation of Simvastatin in microemulsion, it was observed a significant improvement in the potential antiinflammatory and anti-infective properties when the system was use to treat infected wounds (simvastatin pleiotropic effects). Therefore, it can be concluded that the incorporation of these drugs into microemulsion system reveal the potential of microemulsions as a promising and novel dosage form, qualifying them for future trials in order to make them available in the pharmaceutical market |
publishDate |
2010 |
dc.date.issued.fl_str_mv |
2010-06-19 |
dc.date.available.fl_str_mv |
2011-02-07 2014-12-17T14:13:35Z |
dc.date.accessioned.fl_str_mv |
2014-12-17T14:13:35Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/doctoralThesis |
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doctoralThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
DAMASCENO, Bolivar Ponciano Goulart de Lima. Sistemas microemulsionados como carreador lipídico para fármacos insolúveis. 2010. 202 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal do Rio Grande do Norte, Natal, 2010. |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufrn.br/jspui/handle/123456789/13194 |
identifier_str_mv |
DAMASCENO, Bolivar Ponciano Goulart de Lima. Sistemas microemulsionados como carreador lipídico para fármacos insolúveis. 2010. 202 f. Tese (Doutorado em Ciências da Saúde) - Universidade Federal do Rio Grande do Norte, Natal, 2010. |
url |
https://repositorio.ufrn.br/jspui/handle/123456789/13194 |
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por |
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Universidade Federal do Rio Grande do Norte |
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Programa de Pós-Graduação em Ciências da Saúde |
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UFRN |
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BR |
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Ciências da Saúde |
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Universidade Federal do Rio Grande do Norte |
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