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Desenvolvimento de Sistemas Microparticulados Superparamagn?ticos Gastro-resistentes para Diagn?stico e Terap?uticaSilva, Amanda Karine Andriola 16 December 2008 (has links)
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Previous issue date: 2008-12-16 / This work aimed to develop a suitable magnetic system for administration by the oral route. In addition to that, it was intended to review the current uses of magnetic systems and the safety related to magnetic field exposure. Methods:
Coprecipitation and emulsification/crosslinking were carried out in order to synthesize magnetite particles and to coat them, respectively. Results: According to literature
review, it was found that magnetic particles present several properties such as magnetophoresis in magnetic field gradient, production of a surrounding magnetic field, and heat generation in alternated magnetic field. When the human organism is exposed to magnetic fields, several interaction mechanisms come into play. However, biological tissues present low magnetic susceptibility. As a result, the
effects are not so remarkable. Concerning the development of a magnetic system for oral route, uncoated magnetite particles did undergo significant dissolution at gastric
pH. On the other hand, such process was inhibited in the xylan-coated particles. Conclusions: Due to their different properties, magnetic systems have been widely used in biosciences. However, the consequent increased human exposure to magnetic fields has been considered relatively safe. Concerning the experimental work, it was developed a polymer-coated magnetic system. It may be very promising for administration by the oral route for therapy and diagnostic applications as dissolution at gastric pH hardly took place / Realizar um trabalho multidisciplinar a fim de revisar os usos biom?dicos de sistemas magn?ticos, analisar os aspectos sobre a seguran?a relativa ? exposi??o de organismos vivos a campos magn?ticos e desenvolver um sistema magn?tico apropriado para administra??o por via oral. Metodologia: Inicialmente, part?culas magn?ticas foram produzidas pela coprecipita??o de sais de ferro no meio alcalino. A etapa seguinte consistiu no processo de emulsifica??o/reticula??o interfacial realizado a fim de produzir part?culas magn?ticas revestidas por xilana. Resultados: Constata-se que as part?culas magn?ticas apresentam diversas propriedades tais como mobilidade magnetofor?tica em gradiente de campo magn?tico, produ??o de um campo magn?tico capaz de influenciar a regi?o em sua volta e gera??o de calor em campo magn?tico alternado. A exposi??o a campos magn?ticos implica em diversos mecanismos de intera??o, mas os efeitos tendem a ser m?nimos em virtude da baixa susceptibilidade magn?tica dos tecidos. Quanto ao uso
de part?culas de magnetita por via oral, os dados sobre a caracteriza??o das amostras e os resultados do teste de dissolu??o in vitro em pH g?strico demonstraram a viabilidade do m?todo de revestimento apresentado para proteger as part?culas de magnetita da dissolu??o g?strica. Conclus?es: Devido ?s suas diferentes propriedades, os sistemas
magn?ticos t?m encontrado ampla aplicabilidade em ci?ncias biom?dicas, sendo o conseq?ente aumento da exposi??o humana a campo considerado relativamente seguro.
Experimentalmente, foi desenvolvido um sistema magn?tico promissor para administra??o por via oral, que poder? encontrar aplicabilidade como marcador de motilidade intestinal, contraste para resson?ncia nuclear magn?tica ou para a vetoriza??o de f?rmacos
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Novos sistemas de libera??o de f?rmacos ? base de xilanaOliveira, Elquio Eleamen 07 June 2010 (has links)
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Previous issue date: 2010-06-07 / Universidade Federal do Rio Grande do Norte / The aim of this work was to perform the extraction and characterization of xylan from corn cobs and prepare xylan-based microcapsules. For that purpose, an alkaline extraction of xylan was carried out followed by the polymer
characterization regarding its technological properties, such as angle of repose, Hausner factor, density, compressibility and compactability. Also, a low-cost and rapid analytical procedure to identify xylan by means of infrared spectroscopy was studied. Xylan was characterized as a yellowish fine powder with low density and poor flow properties. After the extraction and characterization of the polymer, xylan-based microcapsules were prepared by means of interfacial crosslinking polymerization and their characterization was performed in order to obtain gastroresistant multiparticulate systems. This work involved the most suitable parameters of the preparation of microcapsules as well as the study of the process, scale-up methodology and biological analysis. Magnetic nanoparticles were used as a model system to be encapsulated by the xylan microcapsules. According to the results, xylan-based microcapsules were shown to be resistant to several conditions found along the gastrointestinal tract and they were able to avoid the early degradation of the magnetic nanoparticles / O presente trabalho teve como objetivo a extra??o e caracteriza??o do pol?mero de xilana a partir de res?duos de sabugo de milho e a produ??o de microc?psulas a partir deste pol?mero. O primeiro passo foi a extra??o da xilana em meio alcalino e caracteriza??o deste pol?mero quanto as suas propriedades tecnol?gicas (?ngulo de repouso, fator de Hausner, densidade, compressibilidade e compactabilidade), bem como a elabora??o de uma procedimento r?pido e barato para a identifica??o deste pol?mero atrav?s de espectroscopia de absor??o na regi?o do infravermelho. O pol?mero de xilana foi caracterizado como sendo um p? de cor amarelada de baixa densidade e com propriedades de escoamento pouco favor?veis. Ap?s a obten??o e caracteriza??o do pol?mero, microc?psulas
de xilana foram preparadas atrav?s da reticula??o polim?rica interfacial e caracterizadas a fim de se obter sistemas multiparticulados gastroresistentes. O trabalho foi delineado buscando-se os melhores fatores na t?cnica de prepara??o
das microc?psulas, assim como o estudo do processo, aumento de escala e avalia??o biol?gica. Nanopart?culas magn?ticas foram utilizadas como sistema modelo a ser encapsulado pelas microc?psulas ? base de xilana. Os resultados obtidos demonstraram que as microc?psulas de xilana s?o resistentes ?s diversas condi??es encontradas ao longo do trato gastrintestinal e foram capazes de evitar a degrada??o pr?via das nanopart?culas magn?ticas in vitro
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Nanotechnological delivery systems for the oral administration of active molecules: Polymeric microparticles and microemulsions applied to anti-inflammatory and anti-infectious drugsSilva, Acarilia Eduardo da 05 April 2013 (has links)
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Previous issue date: 2013-04-05 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico / This thesis was devoted to the development of innovative oral delivery systems for two
different molecules. In the first part, microparticles (MPs) based on xylan and Eudragit? S-
100 were produced and used to encapsulate 5-aminosalicylic acid for colon delivery. Xylan
was extracted from corn cobs and characterized in terms of its physicochemical, rheological
and toxicological properties. The polymeric MPs were prepared by interfacial cross-linking
polymerization and spray-drying and characterized for their morphology, mean size and
distribution, thermal stability, crystallinity, entrapment efficiency and in vitro drug release.
MPs with suitable physical characteristics and satisfactory yields were prepared by both
methods, although the spray-dried systems showed higher thermal stability. In general, spraydried
MPs would be preferable systems due to their thermal stability and absence of toxic
agents used in their preparation. However, drug loading and release need to be optimized. In
the second part of this thesis, oil-in-water microemulsions (O/W MEs) based on mediumchain
triglycerides were formulated as drug carriers and solubility enhancers for amphotericin
B (AmB). Phase diagrams were constructed using surfactant blends with hydrophiliclipophilic
balance values between 9.7 and 14.4. The drug-free and drug-loaded MEs presented
spherical non-aggregated droplets around 80 and 120 nm, respectively, and a low
polydispersity index. The incorporation of AmB was high and depended on the volume
fraction of the disperse phase. These MEs did not reduce the viability of J774.A1
macrophage-like cells for concentrations up to 25 μg/mL of AmB. Therefore, O/W MEs
based on propylene glycol esters of caprylic acid may be considered as suitable delivery
systems for AmB / Esta tese teve como objetivo o desenvolvimento de novos sistemas de libera??o para duas
mol?culas distintas. Na primeira parte, micropart?culas ? base de xilana e Eudragit? S-100
foram produzidas para encapsular ?cido 5-aminosalic?lico visando ? libera??o c?lonespec?fica.
A xilana foi extra?da de sabugos de milho e caracterizada quanto ?s suas
propriedades f?sico-qu?micas, reol?gicas e toxicol?gicas. Em seguida, dois m?todos de
microencapsula??o foram utilizados: reticula??o interfacial polim?rica e secagem por
aspers?o. Os sistemas produzidos foram caracterizados quanto ? morfologia, tamanho m?dio e
distribui??o, estabilidade t?rmica, cristalinidade, taxa de encapsula??o e libera??o do f?rmaco
in vitro. Foram obtidas micropart?culas com adequadas caracter?sticas f?sicas e rendimentos
satisfat?rios atrav?s dos dois m?todos, embora os sistemas aspergidos tenham apresentado
maior estabilidade t?rmica e sejam considerados mais interessantes devido a sua maior
estabilidade t?rmica e aus?ncia de agentes t?xicos. No entanto, ajustes precisam ser feitos
para melhorar a encapsula??o e libera??o do f?rmaco. Na segunda parte, microemuls?es do
tipo ?leo em ?gua (MEs O/A) com base em triglicer?deos de cadeia m?dia (MCT) foram
produzidas visando ao carreamento de anfotericina B (AmB) e aumento da sua solubilidade.
Foram obtidas MEs O/A sem e com AmB com got?culas em torno de 80 e 120 nm,
respectivamente, e ?ndices de polidispers?o de 0,25 e 0,31, respectivamente. A taxa de
incorpora??o da AmB foi alta e dependente do volume da fase dispersa. A viabilidade celular
n?o foi afetada at? 25 μg/mL da AmB. Portanto, MEs O/A a partir de MCT podem ser
promissores sistemas de libera??o para AmB
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Micropart?culas polim?ricas ? base de xilana e Eudragit? S-100 contendo mesalazina visando ? libera??o c?lon-espec?ficaSilva, Acarilia Eduardo da 10 March 2009 (has links)
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Previous issue date: 2009-03-10 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico / Colon-specific drug delivery systems have attracted increasing attention from the
pharmaceutical industry due to their ability of treating intestinal bowel diseases (IBD), which
represent a public health problem in several countries. In spite of being considered a quite
effective molecule for the treatment of IBD, mesalazine (5-ASA) is rapidly absorbed in the
upper gastrointestinal tract and its systemic absorption leads to risks of adverse effects. The
aim of this work was to develop a microparticulate system based on xylan and Eudragit? S-
100 (ES100) for colon-specific delivery of 5-ASA and evaluate the interaction between the
polymers present in the systems. Additionaly, the physicochemical and rheological properties
of xylan were also evaluated. Initially, xylan was extracted from corn cobs and characterized
regarding the yield and rheological properties. Afterwards, 10 formulations were prepared in
different xylan and ES100 weight ratios by spray-drying the polymer solutions in 0.6N NaOH
and phosphate buffer pH 7.4. In addition, 3 formulations consisting of xylan microcapsules
were produced by interfacial cross-linking polymerization and coated by ES100 by means of
spray-drying in different polymer weight ratios of xylan and ES100. The microparticles were
characterized regarding yield, morphology, homogeneity, visual aspect, crystallinity and
thermal behavior. The polymer interaction was investigated by infrared spectroscopy. The
extracted xylan was presented as a very fine and yellowish powder, with mean particle size
smaller than 40μm. Regarding the rheological properties of xylan, they demonstrated that this
polymer has a poor flow, low density and high cohesiveness. The microparticles obtained
were shown to be spherical and aggregates could not be observed. They were found to present
amorphous structure and have a very high thermal stability. The yield varied according to the
polymer ratios. Moreover, it was confirmed that the interaction between xylan and ES100
occurs only by means of physical aggregation / Sistemas c?lon-espec?ficos t?m atra?do o interesse da ind?stria farmac?utica devido ?
possibilidade de tratarem enfermidades, como as doen?as inflamat?rias intestinais (DII), que
compreendem um problema de sa?de p?blica em muitos pa?ses. Apesar de ser considerada
uma mol?cula bastante eficiente para o tratamento das DII, a mesalazina (5-ASA) ?
rapidamente absorvida no trato gastrintestinal superior e sua absor??o sist?mica leva ?
incid?ncia de s?rios efeitos adversos. Este trabalho teve como objetivos produzir um sistema
polim?rico microparticulado ? base de xilana e Eudragit? S-100 (ES100) para libera??o
c?lon-espec?fica de 5-ASA e avaliar a intera??o entre os pol?meros constituintes do sistema,
al?m de aprofundar a caracteriza??o f?sico-qu?mica e tecnol?gica da xilana. A xilana foi
extra?da a partir de sabugos de milho e caracterizada quanto ao rendimento, granulometria,
cristalinidade, propriedades reol?gicas e comportamento t?rmico. Em seguida, 10
formula??es contendo 5-ASA foram preparadas em diferentes propor??es de xilana e ES100
atrav?s da secagem por aspers?o das solu??es polim?ricas com NaOH 0,6N ou tamp?o-fosfato
pH 7,4, como solvente. Al?m disso, 3 formula??es constitu?das de microc?psulas de xilana
produzidas por reticula??o polim?rica interfacial foram revestidas por ES100 atrav?s de
secagem por aspers?o em diferentes propor??es polim?ricas e empregando-se NaOH 0,6N ou
tamp?o-fosfato pH 7,4, como solvente. As micropart?culas foram avaliadas quanto ao
rendimento, morfologia, granulometria, homogeneidade, aspecto visual, cristalinidade e
comportamento t?rmico. A intera??o entre os pol?meros foi investigada atrav?s da
espectroscopia na regi?o do infravermelho e de an?lises t?rmicas. A xilana extra?da
apresentou-se como um p? muito fino, com tamanho m?dio inferior a 40μm, e com colora??o
opaca levemente amarelada. A avalia??o das propriedades reol?gicas da xilana permitiram a
caracteriza??o desse pol?mero, em seu estado original de p?, como um material de baixa
densidade, fluxo restrito e bastante coesivo. Foram obtidas micropart?culas esf?ricas e sem
presen?a de agregados, com estrutura amorfa, em sua maior parte, e bastate est?veis a
temperaturas elevadas. Al?m disso, confirmou-se que a intera??o entre xilana e ES100 ocorre
apenas por agrega??o f?sica
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