Supercritical fluid (SCF)-assisted preparation of cyclodextrin-based poly(pseudo)rotaxanes for transdermal purposes

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéuticaes_ES
dc.contributor.authorCardoso, Gleidson
dc.contributor.authorGarcía González, Carlos A.
dc.contributor.authorSantos Rosales, Víctor
dc.contributor.authorTaveira, Stephania Fleury
dc.contributor.authorCunha-Filho, Marcilio
dc.contributor.authorConcheiro Nine, Ángel Joaquín
dc.contributor.authorÁlvarez Lorenzo, Carmen
dc.contributor.authorMarreto, Ricardo Neves
dc.date.accessioned2023-11-07T13:01:52Z
dc.date.available2023-11-07T13:01:52Z
dc.date.issued2023-08-09
dc.description.abstractThis study aims to investigate the effect of the preparation of solid dispersions using supercritical CO2 (scCO2) on the physicochemical properties and the performance of supramolecular gels based on polymer-cyclodextrin (CD) interactions (named poly(pseudo)rotaxanes, PPR) envisaging a transdermal administration. Solid dispersions containing Soluplus®, the antihypertensive drug carvedilol (CAR), and CD (αCD or HPβCD) were prepared and characterized by HPLC, XRPD, FTIR, and DSC. PPRs prepared from solid dispersions (SCF gels) and the corresponding physical mixtures (PM gels) were analyzed regarding rheology, morphology, in vitro drug diffusion, and ex vivo drug skin permeation. The application of scCO2 led to the loss of the crystalline lattice of CAR while preserving its chemical identity. On the contrary, αCD crystals were still present in the SCF solid dispersions. SCF gels were more uniform than their corresponding PM, and the supercritical treatment resulted in changes in the rheological behavior, reducing the viscosity. CAR in vitro diffusion was significantly higher (p < 0.05) for the αCD-based SCF gel than its corresponding PM gel. Drug skin permeation showed a significant increase in drug flux from CD-based SCF gels (containing αCD or HPβCD) compared to corresponding PM gels. Additionally, the pretreatment of the skin with αCD exhibited increased CAR permeation, suggesting an interaction between αCD and the skin membrane. Results evidenced that SCF processing decisively modified the properties of the supramolecular gels, particularly those prepared with αCDes_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipOpen Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This research was partially supported by the Brazilian agency Fundação de Apoio à Pesquisa do Estado de Goiás (FAPEG). The work was supported by MCIN/AEI/10.13039/501100011033 (PID 2020-113881RB-I00), Spain, Xunta de Galicia (ED431C 2020/17), and FEDERes_ES
dc.identifier.citationDrug Deliv. and Transl. Res. (2023)es_ES
dc.identifier.doi10.1007/s13346-023-01385-w
dc.identifier.essn2190-3948
dc.identifier.issn2190-393X
dc.identifier.urihttp://hdl.handle.net/10347/31202
dc.journal.titleDrug Delivery and Translational Research
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-113881RB-I00/ES/ARQUITECTURAS 5D PARA MEDICINA REGENERATIVA Y TERAPIA LOCALIZADA/es_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s13346-023-01385-wes_ES
dc.rights© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were madees_ES
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCyclodextrin es_ES
dc.subjectPermeation enhancer es_ES
dc.subjectSolid dispersion es_ES
dc.subjectMicrostructurees_ES
dc.titleSupercritical fluid (SCF)-assisted preparation of cyclodextrin-based poly(pseudo)rotaxanes for transdermal purposeses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationb92aed69-6968-4bcc-a70b-74b7b9191042
relation.isAuthorOfPublicationfbd9d3a4-b1f4-4aff-8472-de22b1c140c4
relation.isAuthorOfPublication44d6632e-65cd-485a-bb67-86df5567793a
relation.isAuthorOfPublication.latestForDiscoveryfbd9d3a4-b1f4-4aff-8472-de22b1c140c4

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