Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Trabalho de conclusão de curso |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://hdl.handle.net/11449/155535 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2017-06-19/000885535.pdf |
Resumo: | Several drugs have low solubility within the human body, decreasing its bioavailability. Currently, several liberation platforms have been studied in order to overcome this limitation. Among the carriers employed, functionalized block copolymers have the advantage of interacting with the drug both hydrophilic and hydrophobically. Thus, the study of these platforms is fundamental for the encapsulation of hydrophobic drugs, allowing a greater time of circulation in the organism. The efficiency of incorporation and controlled release is dependent on the size, morphology and interactions of the copolymer blocks. The study focused on the physico-chemical properties of these materials (colloidal stability and micelle size, polymer chain length and micelle-drug affinity) in order to obtain better incorporation results. The use of these carriers is promising in the development of drug delivery systems. The reduction of the side effects, due to the use of these carriers, will allow the patient a less aggressive and more efficient treatment, improving the quality of life. In this work, the formation of micelles of PEG-co-PCL diblock copolymers with and without folic acid functionalization with varying chain size was evaluated and the efficiency of methotrexate incorporation was evaluated. The synthetic method, in which the monomers were added in the presence of catalyst in an inert atmosphere to a round bottom flask, allowed obtainingsamples with low polydispersity index. The samples were characterized by several techniques, such as: infrared transmittance spectroscopy, proton nuclear magnetic resonance spectroscopy, gel permeation chromatography, thermogravimetry, differential scanning calorimetry andX-ray diffraction. The micellar stability determined from the influence of the pH and temperature on the zeta potential and the hydrodynamic diameter of the micelles, in which the micelles were not influenced by temperature and added at pH values close to 4... |
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Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexatoTecnologia de liberação controladaCopolímeros blocoMicelasFármacosMetotrexatoBlock copolymersSeveral drugs have low solubility within the human body, decreasing its bioavailability. Currently, several liberation platforms have been studied in order to overcome this limitation. Among the carriers employed, functionalized block copolymers have the advantage of interacting with the drug both hydrophilic and hydrophobically. Thus, the study of these platforms is fundamental for the encapsulation of hydrophobic drugs, allowing a greater time of circulation in the organism. The efficiency of incorporation and controlled release is dependent on the size, morphology and interactions of the copolymer blocks. The study focused on the physico-chemical properties of these materials (colloidal stability and micelle size, polymer chain length and micelle-drug affinity) in order to obtain better incorporation results. The use of these carriers is promising in the development of drug delivery systems. The reduction of the side effects, due to the use of these carriers, will allow the patient a less aggressive and more efficient treatment, improving the quality of life. In this work, the formation of micelles of PEG-co-PCL diblock copolymers with and without folic acid functionalization with varying chain size was evaluated and the efficiency of methotrexate incorporation was evaluated. The synthetic method, in which the monomers were added in the presence of catalyst in an inert atmosphere to a round bottom flask, allowed obtainingsamples with low polydispersity index. The samples were characterized by several techniques, such as: infrared transmittance spectroscopy, proton nuclear magnetic resonance spectroscopy, gel permeation chromatography, thermogravimetry, differential scanning calorimetry andX-ray diffraction. The micellar stability determined from the influence of the pH and temperature on the zeta potential and the hydrodynamic diameter of the micelles, in which the micelles were not influenced by temperature and added at pH values close to 4...Diversos fármacos apresentam baixa solubilidade dentro do corpo humano, diminuindo sua biodisponibilidade. Atualmente, diversas plataformas de liberação vêm sendo estudadas a fim de superar tal limitação. Entre os carreadores empregados, os copolímeros em bloco funcionalizados apresentam a vantagem de interagirem com o fármaco tanto hidrofílica quanto hidrofobicamente. Dessa forma, oestudo destas plataformas é fundamental para o encapsulamento de fármacos hidrofóbicos, permitindo um maior tempo de circulação no organismo. A eficiência de incorporação e liberação controlada é dependente do tamanho, morfologia e das interações dos blocos de copolímeros.O estudo se concentrou nas propriedades físico-químicas destes materiais (estabilidade coloidal e tamanho das micelas, tamanho de cadeia polimérica e afinidade micela-fármaco) com a finalidade de obter melhores resultados de incorporação.O uso destes carreadores é promissor no desenvolvimento de sistemas de liberação de fármacos. A diminuição dos efeitos colaterais, em função do uso destes carreadores, permitirá ao paciente um tratamento menos agressivo e mais eficiente, melhorando a qualidade de vida. Neste trabalho, avaliou-se a formação de micelas de copolímeros dibloco PEG-co-PCLcom e sem funcionalizaçãocom ácido fólicocom variado tamanho de cadeia e avaliou-se a eficiência de incorporação demetotrexato.O método sintético, no qual foramadicionados os monômeros na presença de catalisador em atmosfera inerte aum balão de fundo redondo, permitiu a obtenção de amostras com baixo índice de polidispersão. As amostras foram caracterizadas por diversas técnicas, tais como: espectroscopia de transmitância na região do infravermelho, espectroscopia de ressonância magnética nuclear de próton, cromatografia de permeação em gel, termogravimetria, calorimetria exploratória diferencialedifração de raios-X. A estabilidade micelar determinada...Universidade Estadual Paulista (Unesp)Marques, Rodrigo Fernando Costa [UNESP]Universidade Estadual Paulista (Unesp)Brandt, João Victor [UNESP]2018-08-30T18:22:06Z2018-08-30T18:22:06Z2016info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesis60 f.application/pdfBRANDT, João Victor. Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato. 2016. 60 f. Trabalho de conclusão de curso (bacharelado - Química) - Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Química, 2016.http://hdl.handle.net/11449/155535000885535http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2017-06-19/000885535.pdf21159426216941740000-0003-0195-3885Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2023-10-10T06:02:47Zoai:repositorio.unesp.br:11449/155535Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:29:54.129982Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
title |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
spellingShingle |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato Brandt, João Victor [UNESP] Tecnologia de liberação controlada Copolímeros bloco Micelas Fármacos Metotrexato Block copolymers |
title_short |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
title_full |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
title_fullStr |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
title_full_unstemmed |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
title_sort |
Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato |
author |
Brandt, João Victor [UNESP] |
author_facet |
Brandt, João Victor [UNESP] |
author_role |
author |
dc.contributor.none.fl_str_mv |
Marques, Rodrigo Fernando Costa [UNESP] Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Brandt, João Victor [UNESP] |
dc.subject.por.fl_str_mv |
Tecnologia de liberação controlada Copolímeros bloco Micelas Fármacos Metotrexato Block copolymers |
topic |
Tecnologia de liberação controlada Copolímeros bloco Micelas Fármacos Metotrexato Block copolymers |
description |
Several drugs have low solubility within the human body, decreasing its bioavailability. Currently, several liberation platforms have been studied in order to overcome this limitation. Among the carriers employed, functionalized block copolymers have the advantage of interacting with the drug both hydrophilic and hydrophobically. Thus, the study of these platforms is fundamental for the encapsulation of hydrophobic drugs, allowing a greater time of circulation in the organism. The efficiency of incorporation and controlled release is dependent on the size, morphology and interactions of the copolymer blocks. The study focused on the physico-chemical properties of these materials (colloidal stability and micelle size, polymer chain length and micelle-drug affinity) in order to obtain better incorporation results. The use of these carriers is promising in the development of drug delivery systems. The reduction of the side effects, due to the use of these carriers, will allow the patient a less aggressive and more efficient treatment, improving the quality of life. In this work, the formation of micelles of PEG-co-PCL diblock copolymers with and without folic acid functionalization with varying chain size was evaluated and the efficiency of methotrexate incorporation was evaluated. The synthetic method, in which the monomers were added in the presence of catalyst in an inert atmosphere to a round bottom flask, allowed obtainingsamples with low polydispersity index. The samples were characterized by several techniques, such as: infrared transmittance spectroscopy, proton nuclear magnetic resonance spectroscopy, gel permeation chromatography, thermogravimetry, differential scanning calorimetry andX-ray diffraction. The micellar stability determined from the influence of the pH and temperature on the zeta potential and the hydrodynamic diameter of the micelles, in which the micelles were not influenced by temperature and added at pH values close to 4... |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2018-08-30T18:22:06Z 2018-08-30T18:22:06Z |
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 |
BRANDT, João Victor. Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato. 2016. 60 f. Trabalho de conclusão de curso (bacharelado - Química) - Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Química, 2016. http://hdl.handle.net/11449/155535 000885535 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2017-06-19/000885535.pdf 2115942621694174 0000-0003-0195-3885 |
identifier_str_mv |
BRANDT, João Victor. Preparação de copolímeros PEG-PCL modificado com ácido fólico para liberação controlada de metotrexato. 2016. 60 f. Trabalho de conclusão de curso (bacharelado - Química) - Universidade Estadual Paulista Julio de Mesquita Filho, Instituto de Química, 2016. 000885535 2115942621694174 0000-0003-0195-3885 |
url |
http://hdl.handle.net/11449/155535 http://www.athena.biblioteca.unesp.br/exlibris/bd/capelo/2017-06-19/000885535.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 |
60 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 |
|
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1808128368826122240 |