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Self-Micellizing Technology Improves the Properties of Ezetimibe and Increases Its Effect on Hyperlipidemic Rats

dc.contributor.authorTorrado Salmerón, Carlos Félix
dc.contributor.authorGuarnizo Herrero, Victor
dc.contributor.authorCerezo-Garreta, Javier
dc.contributor.authorTorrado Durán, Guillermo
dc.contributor.authorTorrado Durán, Santiago
dc.date.accessioned2023-06-17T08:21:52Z
dc.date.available2023-06-17T08:21:52Z
dc.date.issued2019-12-03
dc.description.abstractThe aim of this work was to develop ezetimibe self-micellizing solid dispersions using Kolliphor® RH40 (MS-K) as a surfactant incorporating ezetimibe (EZ) into the croscarmellose hydrophilic carrier. Different ezetimibe:Kolliphor® ratios were studied to select micellar systems that improve the dissolution properties of ezetimibe. The different formulations were characterized by means of solid state analysis by SEM, powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), and dissolution studies. These physicochemical studies showed a decrease from the crystalline structure of ezetimibe (EZ) to its amorphous state in the micellar systems (MS-K). A rapid dissolution profile was observed in these micellar systems compared to the drug raw material and physical mixture. Efficacy studies were conducted using a high-fat diet that induced hyperlipidemic rats. The micellar system selected (MS-K 1:0.75) revealed a significant improvement in serum levels of total cholesterol (TC), low-density lipoproteins (LDL), and triglycerides (TG) compared to ezetimibe raw material. The histopathological examination of liver tissue also showed that this micellar system exhibited more beneficial effects on liver steatosis compared to ezetimibe raw material (EZ-RM) and the high-fat diet group (HFD). This study suggests that EZ micellar systems using Kolliphor® RH40 could enhance the antihyperlipidemic effect of ezetimibe and reduce liver steatosis.
dc.description.departmentDepto. de Farmacia Galénica y Tecnología Alimentaria
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (MICINN)
dc.description.sponsorshipUniversidad de Madrid
dc.description.sponsorshipRafael Folch Foundation (Carlos Torrado-Salmerón acknowledges a grant awarded by the Rafael Folch Foundation)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/70173
dc.identifier.doi10.3390/pharmaceutics11120647
dc.identifier.issn1999-4923
dc.identifier.officialurlhttps://doi.org/10.3390/pharmaceutics11120647
dc.identifier.urihttps://hdl.handle.net/20.500.14352/6760
dc.issue.number12
dc.journal.titlePharmaceutics
dc.language.isoeng
dc.page.initial647
dc.publisherMDPI
dc.relation.projectID(RTI2018-093940-B-100)
dc.relation.projectIDUCM (910939)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu615.4
dc.subject.keywordEzetimibe
dc.subject.keywordSolid dispersion
dc.subject.keywordMicellar systems
dc.subject.keywordAntihyperlipidemic activity
dc.subject.keywordLiver steatosis
dc.subject.ucmTecnología farmaceútica
dc.titleSelf-Micellizing Technology Improves the Properties of Ezetimibe and Increases Its Effect on Hyperlipidemic Rats
dc.typejournal article
dc.volume.number11
dspace.entity.typePublication
relation.isAuthorOfPublicationde326ef1-85b8-43d7-abd5-4c8e9e7587e0
relation.isAuthorOfPublication29e18f7c-7752-46fd-a102-20545496a15d
relation.isAuthorOfPublication.latestForDiscoveryde326ef1-85b8-43d7-abd5-4c8e9e7587e0

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