Desenvolvimento de plataformas nanotecnológicas para a construção de biossensores: diagnóstico molecular de doenças infecciosas e inflamatórias

In the present thesis, three biosensing platforms aiming the molecular diagnosis of hepatitis C, hepatitis B and rheumatoid arthritis were developed by electrochemical, optical and microscopic techniques using real samples. The genosensors for the diagnosis of hepatitis C and B were developed on a g...

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Detalles Bibliográficos
Autor: Oliveira, Danielle Alves de
Tipo de recurso: tesis doctoral
Estado:Versión publicada
Fecha de publicación:2017
País:Brasil
Institución:Universidade Federal de Uberlândia (UFU)
Repositorio:Repositório Institucional da UFU
Idioma:portugués
OAI Identifier:oai:repositorio.ufu.br:123456789/20919
Acceso en línea:https://repositorio.ufu.br/handle/123456789/20919
http://doi.org/10.14393/ufu.te.2017.160
Access Level:acceso abierto
Palabra clave:Bioquímica
Biossensores
Hepatite B
Hepatite C
Doenças infecciosas
artrite reumatoide
biossensor
óxido de grafeno
peptídeo mimético
genossensor
nanopartícula de ouro
hepatitis B
hepatitis C
rheumatoid arthritis
biosensor
graphene oxide
peptide mimetic
genosensor
gold nanoparticle
CNPQ::CIENCIAS BIOLOGICAS::GENETICA
Descripción
Sumario:In the present thesis, three biosensing platforms aiming the molecular diagnosis of hepatitis C, hepatitis B and rheumatoid arthritis were developed by electrochemical, optical and microscopic techniques using real samples. The genosensors for the diagnosis of hepatitis C and B were developed on a gold electrode modified with nanomaterials, being these graphene oxide and reduced graphene oxide, respectively. In all proposed biosensors the interaction of the probe with the target was effectively verified by the different techniques. In the case of the genossensor for hepatitis C, graphene oxide was chemically modified with ethylenediamine and showed limits of detection and quantification of 1:483 (v/v) and 1:145 (v/v), respectively, using serum samples from positive patients. The interaction of the HCV probe and the gRNA caused a reduction in current response amplitude of about 2.9 fold as compared to the negative control, using the DPV. The genossensor for hepatitis B probe was immobilized on a gold electrode containing reduced graphene oxide, gold disks and gold nanoparticles. Analysis using DPV indicates that the addition of HBV gDNA caused an increase of about 1.4 times in peak current amplitude, when compared to the negative control. In addition, SPR analyzes showed that positive samples of HBV resulted in a change of about 15- fold compared to negative samples. In the biosensor developed for the diagnosis of rheumatoid arthritis, a graphite electrode modified with a poly (3-hydroxybenzoic) film was used, in which a mimetic peptide that recognizes the anti-CAIII antibody was immobilized. The developed mimetic sensor allowed the distinction between positive and negative samples for rheumatoid arthritis, since it presented an decrease in the current signal of about 2.2 times, when compared to the negative serum. Thus, it was possible to develop analytical, selective and specific platforms, providing new approaches for clinical diagnosis and point-of-care applications, for the monitoring of inflammatory and infectious diseases.