Praziquantel-solid lipid nanoparticles produced by supercritical carbon dioxide extraction: physicochemical characterization, release profile, and cytotoxicity

dc.contributor.authorAndrade, Luciana N.
dc.contributor.authorOliveira, Daniele M. L.
dc.contributor.authorChaud, Marco Vinicius
dc.contributor.authorAlves, Thais F. R.
dc.contributor.authorNery, Marcelo
dc.contributor.authorda Silva, Classius F.
dc.contributor.authorGonsalves, Joyce K. C.
dc.contributor.authorNunes, Rogéria S.
dc.contributor.authorCorrea, Cristiane B.
dc.contributor.authorAmaral, Ricardo G.
dc.contributor.authorSánchez-López, E. (Elena)
dc.contributor.authorSouto, Eliana B.
dc.contributor.authorSeverino, Patrícia
dc.date.accessioned2020-06-23T09:23:17Z
dc.date.available2020-06-23T09:23:17Z
dc.date.issued2019-10-28
dc.date.updated2020-06-23T09:23:17Z
dc.description.abstractSolid lipid nanoparticles (SLNs) can be produced by various methods, but most of them are difficult to scale up. Supercritical fluid (SCF) is an important tool to produce micro/nanoparticles with a narrow size distribution and high encapsulation efficiency. The aim of this work was to produce cetyl palmitate SLNs using SCF to be loaded with praziquantel (PZQ) as an insoluble model drug. The mean particle size (nm), polydispersity index (PdI), zeta potential, and encapsulation efficiency (EE) were determined on the freshly prepared samples, which were also subject of Differential Scanning Calorimetry (DSC), Fourier-Transform Infrared Spectroscopy (FTIR), drug release profile, and in vitro cytotoxicity analyses. PZQ-SLN exhibited a mean size of ~25 nm, PdI ~ 0.5, zeta potential ~−28 mV, and EE 88.37%. The DSC analysis demonstrated that SCF reduced the crystallinity of cetyl palmitate and favored the loading of PZQ into the lipid matrices. No chemical interaction between the PZQ and cetyl palmitate was revealed by FTIR analysis, while the release or PZQ from SLN followed the Weibull model. PZQ-SLN showed low cytotoxicity against fibroblasts cell lines. This study demonstrates that SCF may be a suitable scale-up procedure for the production of SLN, which have shown to be an appropriate carrier for PZQ.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec701305
dc.identifier.issn1420-3049
dc.identifier.pmid31661906
dc.identifier.urihttps://hdl.handle.net/2445/166505
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/molecules24213881
dc.relation.ispartofMolecules, 2019, vol. 24, num. 21, p. 3881
dc.relation.urihttps://doi.org/10.3390/molecules24213881
dc.rightscc-by (c) Andrade, Luciana N. et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
dc.subject.classificationFarmacologia
dc.subject.classificationFarmacocinètica
dc.subject.classificationNanotecnologia
dc.subject.otherPharmacology
dc.subject.otherPharmacokinetics
dc.subject.otherNanotechnology
dc.titlePraziquantel-solid lipid nanoparticles produced by supercritical carbon dioxide extraction: physicochemical characterization, release profile, and cytotoxicity
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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