Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral

Detalhes bibliográficos
Autor(a) principal: Costa, Cicero de Oliveira
Data de Publicação: 2006
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da Universidade Federal de Alagoas (UFAL)
Texto Completo: http://repositorio.ufal.br/handle/riufal/1059
Resumo: Analysis of molecular constituents based on natural products has acquired an important perspective in view of the renewed interest in the consumption of herbal prescriptions all over the world. Natural quinonoid compounds possess significant pharmacological properties and are responsible for the bioactivities of several plants. They showed several bioactivities, mainly microbicidal, trypanocidal, virucidal and antitumoral, being also inhibitors of repair systems in cells. Among the quinones, diospyrin is relevant; it is extracted from the stem-bark of Diospyros montana Roxb. It is a bisnaphtoquinone that has significant leishmanicidal activity and in the cancer cells inhibition, by interaction with topoisomerases, enzymes responsible for DNA replication. Due to its importance, it is also necessary to develop simple and accurate methods for its detection, beyond analysis of probable DNA interaction through the use of biosensors. This work shows the electrochemical study of diospyrin in mixed (DMSO/acetate buffer solution, 1:1 v/v, pH* 5.4), using Cyclic Voltammetry (CV) and Square Wave Voltammetry (SWV). We also show the development of a diospyrin sensor in nanomolar concentrations using a chemically modified electrode with cobalt tetrasulphonate phthalocyanine (CoTSPc) and poly-L-lysine (PLL). The diospyrin quantification in plant crude extract was performed, using the described CME, through addition and recovery methods by using Differential Pulse Voltammetry (DPV), technique also used for the DNA interaction study. The diospyrin voltammograms have showed two redox wave couples and, in its quantification, the glassy carbon electrode was modified with CoTSPc immobilized in PLL film. A significant increase was observed in the reduction current of diospyrin, in CoTSPc modified electrode, in a potential of 0.16 V, in comparison with GC bare electrode. The high-observed activity with modified GC electrode can be associated with the catalytic effect of CoTSPc over the reduction reaction of the diospyrin. These results allowed the diospyrin detection in nanomolar concentrations after parameters optimization like CoTSPc (0.6 mmol L-1), PLL (0.5 mmol L-1) and acetate buffer concentrations (0.15 mol L-1), the scan rate (0.035 V s-1) and amplitude (0.09 V) studies. The limits of detection and quantification were 0.3 nmol L-1 and 1.0 nmol L-1, respectively. The developed sensor was used for diospyrin determination in a chloroformic crude extract of stem-bark of D. montana Roxb. and the recovery average for the samples was 101.9 (± 3.1)%. It was observed the diospyrin-DNA interaction through the use of a dsDNA biosensor and the observation of diagnostic oxidation peaks in potentials relative to the oxidation of guanine and adenine nucleobases, after incubation with the analyte.
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spelling Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoralDiospirinaEletroanalíticaLeishmanioseCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ANALITICA::ELETROANALITICAAnalysis of molecular constituents based on natural products has acquired an important perspective in view of the renewed interest in the consumption of herbal prescriptions all over the world. Natural quinonoid compounds possess significant pharmacological properties and are responsible for the bioactivities of several plants. They showed several bioactivities, mainly microbicidal, trypanocidal, virucidal and antitumoral, being also inhibitors of repair systems in cells. Among the quinones, diospyrin is relevant; it is extracted from the stem-bark of Diospyros montana Roxb. It is a bisnaphtoquinone that has significant leishmanicidal activity and in the cancer cells inhibition, by interaction with topoisomerases, enzymes responsible for DNA replication. Due to its importance, it is also necessary to develop simple and accurate methods for its detection, beyond analysis of probable DNA interaction through the use of biosensors. This work shows the electrochemical study of diospyrin in mixed (DMSO/acetate buffer solution, 1:1 v/v, pH* 5.4), using Cyclic Voltammetry (CV) and Square Wave Voltammetry (SWV). We also show the development of a diospyrin sensor in nanomolar concentrations using a chemically modified electrode with cobalt tetrasulphonate phthalocyanine (CoTSPc) and poly-L-lysine (PLL). The diospyrin quantification in plant crude extract was performed, using the described CME, through addition and recovery methods by using Differential Pulse Voltammetry (DPV), technique also used for the DNA interaction study. The diospyrin voltammograms have showed two redox wave couples and, in its quantification, the glassy carbon electrode was modified with CoTSPc immobilized in PLL film. A significant increase was observed in the reduction current of diospyrin, in CoTSPc modified electrode, in a potential of 0.16 V, in comparison with GC bare electrode. The high-observed activity with modified GC electrode can be associated with the catalytic effect of CoTSPc over the reduction reaction of the diospyrin. These results allowed the diospyrin detection in nanomolar concentrations after parameters optimization like CoTSPc (0.6 mmol L-1), PLL (0.5 mmol L-1) and acetate buffer concentrations (0.15 mol L-1), the scan rate (0.035 V s-1) and amplitude (0.09 V) studies. The limits of detection and quantification were 0.3 nmol L-1 and 1.0 nmol L-1, respectively. The developed sensor was used for diospyrin determination in a chloroformic crude extract of stem-bark of D. montana Roxb. and the recovery average for the samples was 101.9 (± 3.1)%. It was observed the diospyrin-DNA interaction through the use of a dsDNA biosensor and the observation of diagnostic oxidation peaks in potentials relative to the oxidation of guanine and adenine nucleobases, after incubation with the analyte.Fundação de Amparo a Pesquisa do Estado de AlagoasA análise de princípios ativos oriundos de produtos naturais apresenta forte interesse em vista do aumento do consumo de ervas medicinais no mundo inteiro. Os compostos quinônicos são os responsáveis diretos pelas propriedades farmacológicas de várias plantas e nestes estudos farmacológicos e biológicos, mostraram variadas bioatividades, destacando-se, dentre muitas, as propriedades microbicidas, tripanossomicidas, viruscidas, antitumorais e inibidoras de sistemas celulares reparadores, processos nos quais atuam de diferentes formas. Dentre as quinonas, destaca-se a diospirina, extraída da casca do caule da planta Diospyros montana Roxb. Ela é uma bisnaftoquinona que possui importante atividade leishmaniscida e na inibição de células cancerígenas, por interação com topoisomerases, que são enzimas imprescindíveis à replicação do DNA. Devido à importância da diospirina, produto natural, além do estudo farmacológico, faz-se necessário o desenvolvimento de métodos simples e eficientes para a sua detecção, além da análise da sua provável interação com o DNA através do uso de biossensores. Este trabalho mostra o estudo eletroquímico da diospirina em meio prótico misto (DMSO/tampão acetato, 1:1 v/v, pH* 5,4), empregando Voltametria Cíclica (VC) e Voltametria de Onda Quadrada (VOQ), além de mostrar o desenvolvimento de um sensor para diospirina em concentrações nanomolares usando um eletrodo quimicamente modificado com ftalocianina tetrassulfonada de cobalto (CoTSPc) e poli-l-lisina (PLL), sua quantificação no extrato bruto da planta através do método de adição e recuperação e o estudo da interação da mesma com o DNA em Voltametria de Pulso Diferencial (VPD). O voltamograma da diospirina indicou a presença de dois pares de ondas e, na sua quantificação, o eletrodo de carbono vítreo foi modificado com CoTSPc imobilizada em filme de PLL. Houve um aumento significativo na corrente de redução da diospirina, em eletrodo modificado com CoTSPc, no potencial de 0,16 V, em comparação com o eletrodo de carbono vítreo. A alta resposta observada com o eletrodo modificado pode estar associada ao efeito catalítico de CoTSPc sobre a reação de redução da diosporina. Este resultado proporcionou a detecção de diospirina em níveis nanomolares após a otimização de parâmetros como o efeito da concentração da CoTSPc (0,6 mmol L-1), de PLL (0,5 mmol L-1), do eletrólito de suporte (0,15 mol L-1) e estudos da velocidade de varredura (0,035 V s-1) e amplitude (0,09 V). Os limites de detecção e quantificação foram respectivamente, 0,3 nmol L-1 e 1,0 nmol L-1. O sensor desenvolvido foi aplicado para a determinação de diospirina no extrato clorofórmico bruto da casca do caule da planta D. montana Roxb. e a taxa de recuperação para estas amostras foi de 101,9 (± 3,1)%. Observou-se a interação da diospirina com o DNA pela utilização do biossensor de dsDNA e observação de picos de oxidação nos potenciais correspondentes à oxidação das nucleobases guanina e adenina, após sua incubação com o analito.Universidade Federal de AlagoasBRQuímica; BiotecnologiaPrograma de Pós-Graduação em Química e BiotecnologiaUFALGoulart, Marília Oliveira FonsecaCPF:14476630472GOULART, M. O. F.Nascimento, Valberes Bernardo doCPF:17508649400NASCIMENTO, V. B.Meneghetti, Simoni Margareti PlentzCPF:40698076087MENEGHETTI, S. M. P.Costa, Cicero de Oliveira2015-08-25T19:05:37Z2007-06-062015-08-25T19:05:37Z2006-07-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfCOSTA, Cicero de Oliveira. Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral. 2006. 106 f. Dissertação (Mestrado em Química; Biotecnologia) - Universidade Federal de Alagoas, Maceió, 2006.http://repositorio.ufal.br/handle/riufal/1059porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Federal de Alagoas (UFAL)instname:Universidade Federal de Alagoas (UFAL)instacron:UFAL2018-10-24T20:14:50Zoai:www.repositorio.ufal.br:riufal/1059Repositório InstitucionalPUBhttp://www.repositorio.ufal.br/oai/requestri@sibi.ufal.bropendoar:2018-10-24T20:14:50Repositório Institucional da Universidade Federal de Alagoas (UFAL) - Universidade Federal de Alagoas (UFAL)false
dc.title.none.fl_str_mv Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
title Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
spellingShingle Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
Costa, Cicero de Oliveira
Diospirina
Eletroanalítica
Leishmaniose
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ANALITICA::ELETROANALITICA
title_short Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
title_full Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
title_fullStr Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
title_full_unstemmed Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
title_sort Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral
author Costa, Cicero de Oliveira
author_facet Costa, Cicero de Oliveira
author_role author
dc.contributor.none.fl_str_mv Goulart, Marília Oliveira Fonseca
CPF:14476630472
GOULART, M. O. F.
Nascimento, Valberes Bernardo do
CPF:17508649400
NASCIMENTO, V. B.
Meneghetti, Simoni Margareti Plentz
CPF:40698076087
MENEGHETTI, S. M. P.
dc.contributor.author.fl_str_mv Costa, Cicero de Oliveira
dc.subject.por.fl_str_mv Diospirina
Eletroanalítica
Leishmaniose
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ANALITICA::ELETROANALITICA
topic Diospirina
Eletroanalítica
Leishmaniose
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA ANALITICA::ELETROANALITICA
description Analysis of molecular constituents based on natural products has acquired an important perspective in view of the renewed interest in the consumption of herbal prescriptions all over the world. Natural quinonoid compounds possess significant pharmacological properties and are responsible for the bioactivities of several plants. They showed several bioactivities, mainly microbicidal, trypanocidal, virucidal and antitumoral, being also inhibitors of repair systems in cells. Among the quinones, diospyrin is relevant; it is extracted from the stem-bark of Diospyros montana Roxb. It is a bisnaphtoquinone that has significant leishmanicidal activity and in the cancer cells inhibition, by interaction with topoisomerases, enzymes responsible for DNA replication. Due to its importance, it is also necessary to develop simple and accurate methods for its detection, beyond analysis of probable DNA interaction through the use of biosensors. This work shows the electrochemical study of diospyrin in mixed (DMSO/acetate buffer solution, 1:1 v/v, pH* 5.4), using Cyclic Voltammetry (CV) and Square Wave Voltammetry (SWV). We also show the development of a diospyrin sensor in nanomolar concentrations using a chemically modified electrode with cobalt tetrasulphonate phthalocyanine (CoTSPc) and poly-L-lysine (PLL). The diospyrin quantification in plant crude extract was performed, using the described CME, through addition and recovery methods by using Differential Pulse Voltammetry (DPV), technique also used for the DNA interaction study. The diospyrin voltammograms have showed two redox wave couples and, in its quantification, the glassy carbon electrode was modified with CoTSPc immobilized in PLL film. A significant increase was observed in the reduction current of diospyrin, in CoTSPc modified electrode, in a potential of 0.16 V, in comparison with GC bare electrode. The high-observed activity with modified GC electrode can be associated with the catalytic effect of CoTSPc over the reduction reaction of the diospyrin. These results allowed the diospyrin detection in nanomolar concentrations after parameters optimization like CoTSPc (0.6 mmol L-1), PLL (0.5 mmol L-1) and acetate buffer concentrations (0.15 mol L-1), the scan rate (0.035 V s-1) and amplitude (0.09 V) studies. The limits of detection and quantification were 0.3 nmol L-1 and 1.0 nmol L-1, respectively. The developed sensor was used for diospyrin determination in a chloroformic crude extract of stem-bark of D. montana Roxb. and the recovery average for the samples was 101.9 (± 3.1)%. It was observed the diospyrin-DNA interaction through the use of a dsDNA biosensor and the observation of diagnostic oxidation peaks in potentials relative to the oxidation of guanine and adenine nucleobases, after incubation with the analyte.
publishDate 2006
dc.date.none.fl_str_mv 2006-07-31
2007-06-06
2015-08-25T19:05:37Z
2015-08-25T19:05:37Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv COSTA, Cicero de Oliveira. Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral. 2006. 106 f. Dissertação (Mestrado em Química; Biotecnologia) - Universidade Federal de Alagoas, Maceió, 2006.
http://repositorio.ufal.br/handle/riufal/1059
identifier_str_mv COSTA, Cicero de Oliveira. Estudos bioeletroquímicos e eletroanalíticos da diospirina : agente leishmanicida e antitumoral. 2006. 106 f. Dissertação (Mestrado em Química; Biotecnologia) - Universidade Federal de Alagoas, Maceió, 2006.
url http://repositorio.ufal.br/handle/riufal/1059
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language por
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dc.publisher.none.fl_str_mv Universidade Federal de Alagoas
BR
Química; Biotecnologia
Programa de Pós-Graduação em Química e Biotecnologia
UFAL
publisher.none.fl_str_mv Universidade Federal de Alagoas
BR
Química; Biotecnologia
Programa de Pós-Graduação em Química e Biotecnologia
UFAL
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal de Alagoas (UFAL)
instname:Universidade Federal de Alagoas (UFAL)
instacron:UFAL
instname_str Universidade Federal de Alagoas (UFAL)
instacron_str UFAL
institution UFAL
reponame_str Repositório Institucional da Universidade Federal de Alagoas (UFAL)
collection Repositório Institucional da Universidade Federal de Alagoas (UFAL)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal de Alagoas (UFAL) - Universidade Federal de Alagoas (UFAL)
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