Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares

Detalhes bibliográficos
Autor(a) principal: Brandão, Maria Cláudia Rodrigues
Data de Publicação: 2017
Tipo de documento: Tese
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFPB
Texto Completo: https://repositorio.ufpb.br/jspui/handle/123456789/13081
Resumo: Cardiovascular diseases are the leading cause of death in the world, killing about 17 million people a year, according to the World Health Organization. The main means of treating these diseases is by controlling the levels of endogenous nitric oxide, whose regulation Depends on the administration of chemical species donor of this oxide. The purpose of this study was to develop new formulations of organic nitrates with potential to act as a pro-drug, starting from low-cost raw material, mainly biofuels co-products and biomass reuse. Seventeen organic nitrates were synthesized, thirteen of them being unpublished molecules, all obtained in excellent yields and satisfactorily characterized by 1H NMR, 13C NMR and IV spectroscopy. To this end, in addition to commercially available reagents, was used crude glycerine obtained from the production of biodiesel, previously treated and purified, higher alcohols distillate of the fusel oil, which is a by-product of ethanol production, and furfural which is a derivative of lignocellulose. These compounds were synthesized from the nitration of alcohols and alkoxy ethers by reaction with nitric acid, and chloro esters by reaction with silver nitrate. The in silico studies indicate that these molecules present excellent potential for drugs, presenting low toxicity, and taking into account the physicochemical parameters that are determinant in the absorption, distribution, metabolism and excretion of a drug. All tests of cardiovascular activity performed were satisfactory, demonstrating that the synthesized nitrates have a vasorelaxant potential equal to or greater than the reference compounds, with the advantage of not provoking oxidative stress and consequent tolerance to the drug. In general, it was verified that the proposed changes in the carbon skeleton of the new nitrates developed brought advantages of application to the compounds, with an increase in their beneficial effects attributed also to the increase of the carbon chain.
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spelling Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovascularesNitratos orgânicosDoadores de óxido nítricoVasodilatadoresOrganic nitratesOxide nitric donorsVasodilatorCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICACardiovascular diseases are the leading cause of death in the world, killing about 17 million people a year, according to the World Health Organization. The main means of treating these diseases is by controlling the levels of endogenous nitric oxide, whose regulation Depends on the administration of chemical species donor of this oxide. The purpose of this study was to develop new formulations of organic nitrates with potential to act as a pro-drug, starting from low-cost raw material, mainly biofuels co-products and biomass reuse. Seventeen organic nitrates were synthesized, thirteen of them being unpublished molecules, all obtained in excellent yields and satisfactorily characterized by 1H NMR, 13C NMR and IV spectroscopy. To this end, in addition to commercially available reagents, was used crude glycerine obtained from the production of biodiesel, previously treated and purified, higher alcohols distillate of the fusel oil, which is a by-product of ethanol production, and furfural which is a derivative of lignocellulose. These compounds were synthesized from the nitration of alcohols and alkoxy ethers by reaction with nitric acid, and chloro esters by reaction with silver nitrate. The in silico studies indicate that these molecules present excellent potential for drugs, presenting low toxicity, and taking into account the physicochemical parameters that are determinant in the absorption, distribution, metabolism and excretion of a drug. All tests of cardiovascular activity performed were satisfactory, demonstrating that the synthesized nitrates have a vasorelaxant potential equal to or greater than the reference compounds, with the advantage of not provoking oxidative stress and consequent tolerance to the drug. In general, it was verified that the proposed changes in the carbon skeleton of the new nitrates developed brought advantages of application to the compounds, with an increase in their beneficial effects attributed also to the increase of the carbon chain.NenhumaAs doenças cardiovasculares são a principal causa de mortes no mundo, matando cerca de 17 milhões de pessoas por ano, segundo a Organização Mundial de Saúde. Um dos principais meios de tratamento destas doenças dá-se por controle dos níveis de óxido nítrico endógeno, cuja regulação depende da administração de espécies químicas doadoras deste óxido. O propósito deste estudo foi desenvolver novas formulações de nitratos orgânicos com potencialidades para atuar como pró-fármaco, partindo de matéria-prima de baixo custo, principalmente de coprodutos da indústria de biocombustíveis e reaproveitamento de biomassa. Foram sintetizados dezessete nitratos orgânicos, sendo treze deles moléculas inéditas, todos obtidos com excelentes rendimentos e caracterizados satisfatoriamente por espectroscopia de RMN 1H, RMN 13C e IV. Para tal, além de reagentes comercialmente adquiridos, utilizou-se glicerina bruta obtida da produção de biodiesel, previamente tratada e purificada, álcoois superiores destilados do óleo fúsel, que é um sub-produto da produção de etanol, e furfural que é um derivado da lignocelulose. Estes compostos foram sintetizados a partir da nitração de intermediários tipo álcoois e alcóxi-éteres por reação com ácido nítrico, e cloroésteres por reação com nitrato de prata. Os estudos in silico realizados apontam que estas moléculas apresentam excelente potencial para fármacos, apresentando baixa toxicidade, e atendendo aos parâmetros físico-químicos que são determinantes na absorção, distribuição, metabolismo e excreção de um fármaco. Todos os testes de atividade cardiovascular realizados foram satisfatórios, demonstrando que os nitratos sintetizados possuem potencial vasorrelaxante igual ou superior aos compostos de referência, com a vantagem de não provocarem estresse oxidativo e a consequente tolerância ao fármaco. De modo geral, verificou-se que as mudanças propostas no esqueleto carbônico dos novos nitratos desenvolvidos trouxeram vantagens de aplicação aos compostos, com aumento de seus efeitos benéficos atribuído também ao aumento da cadeia carbônica.Universidade Federal da ParaíbaBrasilQuímicaPrograma de Pós-Graduação em QuímicaUFPBAthayde Filho, Petrônio Filgueiras dehttp://lattes.cnpq.br/1717412318563908Brandão, Maria Cláudia Rodrigues2019-01-24T20:30:01Z2019-01-242019-01-24T20:30:01Z2017-08-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesishttps://repositorio.ufpb.br/jspui/handle/123456789/13081porAttribution-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nd/3.0/br/info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFPBinstname:Universidade Federal da Paraíba (UFPB)instacron:UFPB2019-01-24T20:30:01Zoai:repositorio.ufpb.br:123456789/13081Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufpb.br/PUBhttp://tede.biblioteca.ufpb.br:8080/oai/requestdiretoria@ufpb.br|| diretoria@ufpb.bropendoar:2019-01-24T20:30:01Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB)false
dc.title.none.fl_str_mv Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
title Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
spellingShingle Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
Brandão, Maria Cláudia Rodrigues
Nitratos orgânicos
Doadores de óxido nítrico
Vasodilatadores
Organic nitrates
Oxide nitric donors
Vasodilator
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
title_full Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
title_fullStr Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
title_full_unstemmed Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
title_sort Novos nitratos orgânicos derivados de biomassas como potenciais fármacos cardiovasculares
author Brandão, Maria Cláudia Rodrigues
author_facet Brandão, Maria Cláudia Rodrigues
author_role author
dc.contributor.none.fl_str_mv Athayde Filho, Petrônio Filgueiras de
http://lattes.cnpq.br/1717412318563908
dc.contributor.author.fl_str_mv Brandão, Maria Cláudia Rodrigues
dc.subject.por.fl_str_mv Nitratos orgânicos
Doadores de óxido nítrico
Vasodilatadores
Organic nitrates
Oxide nitric donors
Vasodilator
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic Nitratos orgânicos
Doadores de óxido nítrico
Vasodilatadores
Organic nitrates
Oxide nitric donors
Vasodilator
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description Cardiovascular diseases are the leading cause of death in the world, killing about 17 million people a year, according to the World Health Organization. The main means of treating these diseases is by controlling the levels of endogenous nitric oxide, whose regulation Depends on the administration of chemical species donor of this oxide. The purpose of this study was to develop new formulations of organic nitrates with potential to act as a pro-drug, starting from low-cost raw material, mainly biofuels co-products and biomass reuse. Seventeen organic nitrates were synthesized, thirteen of them being unpublished molecules, all obtained in excellent yields and satisfactorily characterized by 1H NMR, 13C NMR and IV spectroscopy. To this end, in addition to commercially available reagents, was used crude glycerine obtained from the production of biodiesel, previously treated and purified, higher alcohols distillate of the fusel oil, which is a by-product of ethanol production, and furfural which is a derivative of lignocellulose. These compounds were synthesized from the nitration of alcohols and alkoxy ethers by reaction with nitric acid, and chloro esters by reaction with silver nitrate. The in silico studies indicate that these molecules present excellent potential for drugs, presenting low toxicity, and taking into account the physicochemical parameters that are determinant in the absorption, distribution, metabolism and excretion of a drug. All tests of cardiovascular activity performed were satisfactory, demonstrating that the synthesized nitrates have a vasorelaxant potential equal to or greater than the reference compounds, with the advantage of not provoking oxidative stress and consequent tolerance to the drug. In general, it was verified that the proposed changes in the carbon skeleton of the new nitrates developed brought advantages of application to the compounds, with an increase in their beneficial effects attributed also to the increase of the carbon chain.
publishDate 2017
dc.date.none.fl_str_mv 2017-08-25
2019-01-24T20:30:01Z
2019-01-24
2019-01-24T20:30:01Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.ufpb.br/jspui/handle/123456789/13081
url https://repositorio.ufpb.br/jspui/handle/123456789/13081
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nd/3.0/br/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nd/3.0/br/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal da Paraíba
Brasil
Química
Programa de Pós-Graduação em Química
UFPB
publisher.none.fl_str_mv Universidade Federal da Paraíba
Brasil
Química
Programa de Pós-Graduação em Química
UFPB
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFPB
instname:Universidade Federal da Paraíba (UFPB)
instacron:UFPB
instname_str Universidade Federal da Paraíba (UFPB)
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institution UFPB
reponame_str Biblioteca Digital de Teses e Dissertações da UFPB
collection Biblioteca Digital de Teses e Dissertações da UFPB
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da UFPB - Universidade Federal da Paraíba (UFPB)
repository.mail.fl_str_mv diretoria@ufpb.br|| diretoria@ufpb.br
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