Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors

Detalhes bibliográficos
Autor(a) principal: Daldal,Y. Doğan
Data de Publicação: 2016
Outros Autores: Demiralay,Ebru Çubuk, Ozkan,Sibel A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000300493
Resumo: Reversible acetylcholinesterase inhibitors are an important group of drug compounds that are used medicinally to treat Alzheimer's disease. In this study, dissociation constant values (pKa) of some reversible acetylcholinesterase inhibitors (donepezil, rivastigmine and galantamine) having different functional groups were determined in different percentages of acetonitrile (MeCN)-water and methanol (MeOH)-water binary mixtures using reversed phase liquid chromatography (RPLC) method. In this way, a complete description of the retention behavior of each solute in the space defined by the pH and organic modifier percentages variables was obtained. The linear relationships established between retention factors of the species and the polarity parameter of the mobile phase (ETN) was proved to predict accurately retention in liquid chromatography (LC) as a function of the acetonitrile and methanol content. In result, the estimated aqueous pKa values of studied basic compounds were assessed by comparing them with literature data.
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spelling Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitorsreversible acetylcholinesterase inhibitorsdissociation constantnonlinear regressionpolarity parameterRPLCReversible acetylcholinesterase inhibitors are an important group of drug compounds that are used medicinally to treat Alzheimer's disease. In this study, dissociation constant values (pKa) of some reversible acetylcholinesterase inhibitors (donepezil, rivastigmine and galantamine) having different functional groups were determined in different percentages of acetonitrile (MeCN)-water and methanol (MeOH)-water binary mixtures using reversed phase liquid chromatography (RPLC) method. In this way, a complete description of the retention behavior of each solute in the space defined by the pH and organic modifier percentages variables was obtained. The linear relationships established between retention factors of the species and the polarity parameter of the mobile phase (ETN) was proved to predict accurately retention in liquid chromatography (LC) as a function of the acetonitrile and methanol content. In result, the estimated aqueous pKa values of studied basic compounds were assessed by comparing them with literature data.Sociedade Brasileira de Química2016-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000300493Journal of the Brazilian Chemical Society v.27 n.3 2016reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20150276info:eu-repo/semantics/openAccessDaldal,Y. DoğanDemiralay,Ebru ÇubukOzkan,Sibel A.eng2016-03-10T00:00:00Zoai:scielo:S0103-50532016000300493Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2016-03-10T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
title Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
spellingShingle Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
Daldal,Y. Doğan
reversible acetylcholinesterase inhibitors
dissociation constant
nonlinear regression
polarity parameter
RPLC
title_short Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
title_full Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
title_fullStr Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
title_full_unstemmed Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
title_sort Effect of Organic Solvent Composition on Dissociation Constants of Some Reversible Acetylcholinesterase Inhibitors
author Daldal,Y. Doğan
author_facet Daldal,Y. Doğan
Demiralay,Ebru Çubuk
Ozkan,Sibel A.
author_role author
author2 Demiralay,Ebru Çubuk
Ozkan,Sibel A.
author2_role author
author
dc.contributor.author.fl_str_mv Daldal,Y. Doğan
Demiralay,Ebru Çubuk
Ozkan,Sibel A.
dc.subject.por.fl_str_mv reversible acetylcholinesterase inhibitors
dissociation constant
nonlinear regression
polarity parameter
RPLC
topic reversible acetylcholinesterase inhibitors
dissociation constant
nonlinear regression
polarity parameter
RPLC
description Reversible acetylcholinesterase inhibitors are an important group of drug compounds that are used medicinally to treat Alzheimer's disease. In this study, dissociation constant values (pKa) of some reversible acetylcholinesterase inhibitors (donepezil, rivastigmine and galantamine) having different functional groups were determined in different percentages of acetonitrile (MeCN)-water and methanol (MeOH)-water binary mixtures using reversed phase liquid chromatography (RPLC) method. In this way, a complete description of the retention behavior of each solute in the space defined by the pH and organic modifier percentages variables was obtained. The linear relationships established between retention factors of the species and the polarity parameter of the mobile phase (ETN) was proved to predict accurately retention in liquid chromatography (LC) as a function of the acetonitrile and methanol content. In result, the estimated aqueous pKa values of studied basic compounds were assessed by comparing them with literature data.
publishDate 2016
dc.date.none.fl_str_mv 2016-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000300493
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000300493
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20150276
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.27 n.3 2016
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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