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Previous issue date: 2014-12-11 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPES / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico - CNPq / Quitina ? segundo polissacar?deo mais abundante na natureza e seu derivado
quitosana tem sido amplamento estudado, devido a suas propriedades qu?micas e
farmacol?gicas singulares. Contudo, estudos mostram que essa mol?cula quando no
organismo, tende a se acumular no tecido renal e tamb?m promove um aumento na
excre??o de c?lcio. Apesar disso, o efeito da quitosana sobre a forma??o de cristais
de oxalato de c?lcio (OxCa) nunca foi avaliado. A forma??o de c?lculos renais
(urolit?ase) ? a enfermidade que mais comumente afeta os rins e o sistema urin?rio,
al?m de ser uma doen?a que possui altas preval?ncia e recorr?ncia. Muitas
mol?culas com capacidade antioxidante tem demonstrado potencial para diminuir a
forma??o de cristais de OxCa in vitro. Diante do exposto o objetivo desse trabalho foi
avaliar o potencial antioxidante e de interfer?ncia na forma??o de cristais de uma
quitosana de baixo peso molecular e seus derivados conjugados com ?cido g?lico
(AG). As analises f?sico-qu?micas confirmaram a identidade da quitosana. Esta foi
submetida a 5 testes antioxidantes e apresentou uma excelente atividade quelante
de cobre, por?m nenhuma outra atividade antioxidante expressiva foi detectada. J?
quando submetida aos testes de forma??o de cristais in vitro, a quitosana aumentou
o n?mero de cristais de OxCa monohidratados formados, modificou a morfologia
desses cristais, modificou as propor??es entre popula??es de cristais em solu??o e
aumentou o potencial zeta desses cristais formados. Foram obtidas quatro
mol?culas de quitosana conjugadas com AG. As an?lises f?sico-qu?micas
confirmaram que houve liga??o covalente entre quitosana e AG, por?m, n?o se
observou uma conjuga??o de AG de forma dose-dependente. Quando estes
derivados foram submetidas a testes antioxidantes, todas as quitosanas conjugadas
apresentaram potencial antioxidante maior que seus percussores. Contudo, houve
diferen?a de atividade entre as diferentes quitosanas conjugadas, indicando que a
posi??o onde o AG est? conjugado ? um fator importante para determina??o da
atividade. Quando as quitosanas conjugadas foram submetidas aos testes de
forma??o de cristais in vitro, houve uma redu??o na quantidade de cristais
observados quando comparados com aqueles formados na presen?a da quitosana
n?o-conjugada. A quitosana possui uma forte capacidade indutora de forma??o de
cristais de OxCa monohidratados, bem como modifica sua morfologia e potencial
zeta. O processo de conjuga??o de AG ? quitosana levou a um aumento no
potencial antioxidante dessa mol?cula e tamb?m foi capaz de diminuir sua
capacidade de induzir ? forma??o de cristais in vitro / Chitin is the second most abundant polysaccharide in nature and its derivative
chitosan has been widely studied due to its unique chemical and pharmacological
properties. However, studies show that when this molecule is used as food, drug, etc.
it tends to accumulate in renal tissue and promotes an increase in calcium excretion.
Nevertheless, the effect of chitosan on the formation of calcium oxalate (OxCa)
crystals has never been evaluated. The formation of kidney stones (urolithiasis) is the
disease that most often affects the kidneys and the urinary system. In addition, this is
a disease with high prevalence and recurrence. Many molecules with antioxidant
activity have been shown to decrease the potential for in vitro OxCa crystals
formation. Thus, the aim of this study was to evaluate the effect of low molecular
weight chitosan and its derivatives conjugated to gallic acid (AG) as antioxidant and
inhibitor of OxCa crystals formation. The physico-chemical analysis confirmed the
identity of chitosan. This molecule was subjected to five antioxidant tests and showed
an excellent copper chelating activity. However, chitosan did not show other
significant antioxidant activity. When chitosan was subjected to in vitro crystal
formation tests, it increased the number of OxCa monohydrate crystals, modified the
morphology of the crystals, modified the proportions between populations of crystals
in solution and increased the zeta potential of these crystals formed. Four molecules
of chitosan conjugated with GA were obtained. The physico-chemical analysis
confirmed that chitosan and AG were covalently bonded. However, the amount of GA
liked to chitosan did not increase even when 10 times more GA was used in
experiment. When these derivatives were subjected to antioxidant tests, all chitosan
conjugates showed higher antioxidant potential than their precursors. However, they
showed different activity between them, which indicating that the position where AG
is conjugated is an important factor for chitosan-GA activity. When conjugated
chitosans were submitted to in vitro crystal formation tests, a reduction in the crystals
number was observed when compared with those formed in the presence of
unconjugated chitosan. Chitosan has a strong capacity for inducing OxCa
monohydrate crystal formation, as well as modify their morphology and zeta
potential. Over all, the process of conjugating AG to chitosan led to an increase in
antioxidant potential of this molecule and was also able to decrease its capacity of
inducing in vitro crystal formation
| Identifer | oai:union.ndltd.org:IBICT/oai:repositorio.ufrn.br:123456789/19620 |
| Date | 11 December 2014 |
| Creators | Queiroz Neto, Moacir Fernandes de |
| Contributors | 76111830449, http://lattes.cnpq.br/4651814546820796, Farias, Eduardo Henrique Cunha de, 01164378473, http://lattes.cnpq.br/0933304924768138, Costa, Leandro Silva, 04647720446, http://lattes.cnpq.br/4991977240761750, Rocha, Hugo Alexandre de Oliveira |
| Publisher | Universidade Federal do Rio Grande do Norte, PROGRAMA DE P?S-GRADUA??O EM BIOQU?MICA, UFRN, Brasil |
| Source Sets | IBICT Brazilian ETDs |
| Language | Portuguese |
| Detected Language | English |
| Type | info:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis |
| Source | reponame:Repositório Institucional da UFRN, instname:Universidade Federal do Rio Grande do Norte, instacron:UFRN |
| Rights | info:eu-repo/semantics/openAccess |
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