Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106826
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dc.contributor.authorBarros, Marisa C. F.-
dc.contributor.authorRibeiro, Ana C. F.-
dc.contributor.authorEsteso, Miguel Á.-
dc.date.accessioned2023-04-26T08:11:58Z-
dc.date.available2023-04-26T08:11:58Z-
dc.date.issued2018-12-21-
dc.identifier.issn2218-273Xpt
dc.identifier.urihttps://hdl.handle.net/10316/106826-
dc.description.abstractParkinson's disease is a movement disorder characterized by a progressive degeneration of dopaminergic neurons that has been object of study by the scientific community through the last decades. However, nowadays there is still no treatment to cure it, although there are drugs available, with limited efficacy, to relieve the symptoms or replenish the cells with dopamine to supply the lack of dopaminergic neurons. This work was structured in two parts. In the first one, binary aqueous solutions of L-dopa and cyclodextrins were studied. In the second part, ternary aqueous solutions of L-dopa were studied with each of the selected cyclodextrins. In all cases, thermodynamic properties (density, partial molar volume and thermodynamic transfer functions for temperatures between 294.15 ± 0.01 K and 312.15 ± 0.01 K) and transport properties (mutual diffusion coefficients, viscosity, transfer viscosity at 298.15 ± 0.01 K and 310.15 ± 0.01 K) were studied. Using theoretical models to adjust the experimental data obtained for the diffusion coefficients and for the apparent molar volumes, in the ternary aqueous solutions, it was possible to estimate the values to the L-dopa-cyclodextrin association constant. For the aqueous ternary solutes, the partial molar volume of transfer of levodopa in the presence of the cyclodextrins, the partial molar expansibility at infinite dilution and from this, the Hepler constant, were determined. Also, the values of Gibbs free energy (ΔG⁰), enthalpy (ΔH⁰) and entropy (ΔS⁰) were determined. From the obtained information, it was possible to characterize the molecular interactions, as well as to identify some structural characteristics of the controlled drug delivery systems under study and to estimate the influence of the cyclodextrin substituent groups, and, also, the temperature effect in the interaction levodopa-cyclodextrin. It is our intent to attain information about the mechanism of possible new systems for controlled drug delivery systems, throughout an alternative perspective, which could allow to increase its effectiveness in the Parkinson's treatment.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUID/QUI/UI0313/2013pt
dc.relationCOMPETE Programme (Operational Programme for Competitiveness)pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectParkinsonpt
dc.subjectlevodopapt
dc.subjectcyclodextrinspt
dc.subjectcontrolled drug delivery systemspt
dc.subjecttransport propertiept
dc.subjectthermodynamic propertiespt
dc.subjectdensity; partial molar volumespt
dc.subjectmutual diffusion coefficientspt
dc.subjectviscositypt
dc.subject.meshCyclodextrinspt
dc.subject.meshDiffusionpt
dc.subject.meshHumanspt
dc.subject.meshLevodopapt
dc.subject.meshModels, Theoreticalpt
dc.subject.meshParkinson Diseasept
dc.subject.meshTemperaturept
dc.subject.meshThermodynamicspt
dc.subject.meshViscositypt
dc.titleCyclodextrins in Parkinson's Diseasept
dc.typearticle-
degois.publication.firstPage3pt
degois.publication.issue1pt
degois.publication.titleBiomoleculespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/biom9010003pt
degois.publication.volume9pt
dc.date.embargo2018-12-21*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-4245-759X-
crisitem.author.orcid0000-0002-3005-1963-
crisitem.author.orcid0000-0001-9736-3999-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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