Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Tipo de documento: | Trabalho de conclusão de curso |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://hdl.handle.net/11449/140210 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2016-06-17/000863705.pdf |
Resumo: | The antibiotics of systemic release can cause bacterial resistance and are administered in high doses, causing high toxicity to organs. Metronidazole has potent activity against the majority of anaerobic gram-positive and gram-negative bacteria and protozoa; and its topical administration can be advantageous because of the few systemic effects. However, the use of this route of administration presents a great obstacle due to the difficulty of the permeation of molecules through the stratum corneum. Therefore, it becomes necessary to develop drug delivery systems, such as liquid-crystal systems (LCS) with cationic polymeric adjuvants, to allow the use of this route of administration with therapeutic success. This project aimed to develop an LCS constituted by cetyl alcohol ethoxylate and propxilado (Procetyl® AWS) as surfactant (T), oleic acid as the oil phase (OF) and aqueous phase (AP) containing polymer dispersion of chitosan (F1), polyethyleneimine (F2) or association of polymers (F3) to metronidazole administration. Systems have been developed using polymer dispersions, Procetyl® AWS and oleic acid, it is possible to define regions as transparent liquid system (TLS), translucent liquid system (TRLS), opaque liquid system (OLS), transparent viscous system (TVS), translucent low viscosity system (TRLVS), translucent high viscosity system (TRHVS), opaque viscous system (OVS) or phase separation (PS). One formulation of each system was selected for the characterization tests, determining the concentration of T and AF in 40% and of OF in 20%.The analysis of polarized light microscopy showed anisotropic structures in the form of splines, characteristics of hexagonal phase, for formulations F1, F2 and F3. Rheological tests showed thixotropic behavior of the formulations. The MTZ was incorporated at 0.5% in the formulations, which are now called F1-F, F2-F and F3-F. Release tests showed that the formulations F1-F, F2-F, and F3-F released drug... |
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Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazolQuitosanaMetronidazolPolímerosChitosanThe antibiotics of systemic release can cause bacterial resistance and are administered in high doses, causing high toxicity to organs. Metronidazole has potent activity against the majority of anaerobic gram-positive and gram-negative bacteria and protozoa; and its topical administration can be advantageous because of the few systemic effects. However, the use of this route of administration presents a great obstacle due to the difficulty of the permeation of molecules through the stratum corneum. Therefore, it becomes necessary to develop drug delivery systems, such as liquid-crystal systems (LCS) with cationic polymeric adjuvants, to allow the use of this route of administration with therapeutic success. This project aimed to develop an LCS constituted by cetyl alcohol ethoxylate and propxilado (Procetyl® AWS) as surfactant (T), oleic acid as the oil phase (OF) and aqueous phase (AP) containing polymer dispersion of chitosan (F1), polyethyleneimine (F2) or association of polymers (F3) to metronidazole administration. Systems have been developed using polymer dispersions, Procetyl® AWS and oleic acid, it is possible to define regions as transparent liquid system (TLS), translucent liquid system (TRLS), opaque liquid system (OLS), transparent viscous system (TVS), translucent low viscosity system (TRLVS), translucent high viscosity system (TRHVS), opaque viscous system (OVS) or phase separation (PS). One formulation of each system was selected for the characterization tests, determining the concentration of T and AF in 40% and of OF in 20%.The analysis of polarized light microscopy showed anisotropic structures in the form of splines, characteristics of hexagonal phase, for formulations F1, F2 and F3. Rheological tests showed thixotropic behavior of the formulations. The MTZ was incorporated at 0.5% in the formulations, which are now called F1-F, F2-F and F3-F. Release tests showed that the formulations F1-F, F2-F, and F3-F released drug...Os antimicrobianos de liberação sistêmica podem causar resistência bacteriana e são administrados em elevadas dosagens, causando alta toxicidade aos órgãos. O metronidazol apresenta ação potente contra a maioria das bactérias anaeróbicas gram-positivas e gram-negativas e protozoários; e sua administração cutânea pode ser vantajosa, em razão dos poucos efeitos sistêmicos. Porém, a utilização dessa via de administração apresenta um grande obstáculo, devido à dificuldade da permeação de moléculas pelo estrato córneo. Portanto, torna-se necessário o desenvolvimento de sistemas de liberação de fármacos, como os sistemas líquidocristalinos (SLC) com adjuvantes poliméricos catiônicos, para possibilitar o uso dessa via de administração com sucesso terapêutico. Esse trabalho teve como objetivo de desenvolver um SLC constituído por álcool cetílico propxilado e etoxilado (Procetyl® AWS) como tensoativo (T), ácido oleico como fase oleosa (FO) e fase aquosa (FA) contendo dispersão polimérica de quitosana (F1), polietilenoimina (F2) ou associação dos polímeros (F3) para administração de metronidazol. Foram desenvolvidos sistemas utilizando dispersões poliméricas, Procetyl® AWS e ácido oleico, sendo possível delimitar regiões como: sistema líquido transparente (SLT), sistema líquido translúcido (SLTR), sistema líquido opaco (SLO), sistema viscoso transparente (SVT), sistema translúcido de baixa viscosidade (STRBV) sistema translúcido de alta viscosidade (STRAV), sistema viscoso opaco (SVO) ou separação de fases (SF). Uma formulação de cada sistema foi selecionada para os ensaios de caracterização, fixando-se a concentração de T e de FA em 40% e de FO em 20%. As análises de microscopia de luz polarizada evidenciaram estruturas anisotrópicas na forma de estrias, características de fase hexagonal, para as formulações F1, F2 e F3. Ensaios reológicos evidenciaram comportamento...Universidade Estadual Paulista (Unesp)Chorilli, Marlus [UNESP]Calixto, Giovana [UNESP]Universidade Estadual Paulista (Unesp)Victorelli, Francesca Damiani [UNESP]2016-07-01T13:09:51Z2016-07-01T13:09:51Z2015-12-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesis76 f.application/pdfVICTORELLI, Francesca Damiani. Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol. 2015. 76 f. , 2015.http://hdl.handle.net/11449/140210863705http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2016-06-17/000863705.pdf1427125996716282Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2024-06-24T15:37:59Zoai:repositorio.unesp.br:11449/140210Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:35:29.842972Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
title |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
spellingShingle |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol Victorelli, Francesca Damiani [UNESP] Quitosana Metronidazol Polímeros Chitosan |
title_short |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
title_full |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
title_fullStr |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
title_full_unstemmed |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
title_sort |
Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol |
author |
Victorelli, Francesca Damiani [UNESP] |
author_facet |
Victorelli, Francesca Damiani [UNESP] |
author_role |
author |
dc.contributor.none.fl_str_mv |
Chorilli, Marlus [UNESP] Calixto, Giovana [UNESP] Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Victorelli, Francesca Damiani [UNESP] |
dc.subject.por.fl_str_mv |
Quitosana Metronidazol Polímeros Chitosan |
topic |
Quitosana Metronidazol Polímeros Chitosan |
description |
The antibiotics of systemic release can cause bacterial resistance and are administered in high doses, causing high toxicity to organs. Metronidazole has potent activity against the majority of anaerobic gram-positive and gram-negative bacteria and protozoa; and its topical administration can be advantageous because of the few systemic effects. However, the use of this route of administration presents a great obstacle due to the difficulty of the permeation of molecules through the stratum corneum. Therefore, it becomes necessary to develop drug delivery systems, such as liquid-crystal systems (LCS) with cationic polymeric adjuvants, to allow the use of this route of administration with therapeutic success. This project aimed to develop an LCS constituted by cetyl alcohol ethoxylate and propxilado (Procetyl® AWS) as surfactant (T), oleic acid as the oil phase (OF) and aqueous phase (AP) containing polymer dispersion of chitosan (F1), polyethyleneimine (F2) or association of polymers (F3) to metronidazole administration. Systems have been developed using polymer dispersions, Procetyl® AWS and oleic acid, it is possible to define regions as transparent liquid system (TLS), translucent liquid system (TRLS), opaque liquid system (OLS), transparent viscous system (TVS), translucent low viscosity system (TRLVS), translucent high viscosity system (TRHVS), opaque viscous system (OVS) or phase separation (PS). One formulation of each system was selected for the characterization tests, determining the concentration of T and AF in 40% and of OF in 20%.The analysis of polarized light microscopy showed anisotropic structures in the form of splines, characteristics of hexagonal phase, for formulations F1, F2 and F3. Rheological tests showed thixotropic behavior of the formulations. The MTZ was incorporated at 0.5% in the formulations, which are now called F1-F, F2-F and F3-F. Release tests showed that the formulations F1-F, F2-F, and F3-F released drug... |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-11 2016-07-01T13:09:51Z 2016-07-01T13:09:51Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/bachelorThesis |
format |
bachelorThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
VICTORELLI, Francesca Damiani. Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol. 2015. 76 f. , 2015. http://hdl.handle.net/11449/140210 863705 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2016-06-17/000863705.pdf 1427125996716282 |
identifier_str_mv |
VICTORELLI, Francesca Damiani. Sistemas líquidos cristalinos a base de quitosana e polietilenoimina para a administração cutânea de metronidazol. 2015. 76 f. , 2015. 863705 1427125996716282 |
url |
http://hdl.handle.net/11449/140210 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2016-06-17/000863705.pdf |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
76 f. application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
publisher.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.source.none.fl_str_mv |
Aleph reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129092548034560 |