Lipid nanocapsules decorated and loaded with cannabidiol as targeted prolonged release carriers for glioma therapy: In vitro screening of critical parameters

dc.contributor.authorAparicio Blanco, Juan
dc.contributor.authorSebastián, Víctor
dc.contributor.authorBenoit, Jean P.
dc.contributor.authorTorres Suárez, Ana Isabel
dc.date.accessioned2024-01-31T12:26:07Z
dc.date.available2024-01-31T12:26:07Z
dc.date.issued2019-01
dc.description.abstractThe therapeutic potential of cannabinoids has been truly constrained heretofore due to their strong psychoactive effects and their high lipophilicity. In this context, precisely due to the lack of psychoactive properties, cannabidiol (CBD), the second major component of Cannabis sativa, arises as the phytocannabinoid with the most auspicious therapeutic potential. Hence, the incorporation of CBD in lipid nanocapsules (LNCs) will contribute to overcome the dosing problems associated with cannabinoids. Herein, we have prepared LNCs decorated and loaded with CBD for glioma therapy and screened in vitro their critical parameters. On the one hand, we have encapsulated CBD into the oily core of LNCs to test their in vitro efficacy as extended-release carriers against the human glioblastoma cell line U373MG. The in vitro antitumor effect was highly dependent on the size of LNCs due to its pivotal role in the extent of CBD release. Effectively, a comparison between two differently-sized LNCs (namely, 20-nm and 50-nm sized carriers) showed that the smaller LNCs reduced by 3.0-fold the IC50 value of their 50-nm sized counterparts. On the other hand, to explore the potential of this phytocannabinoid to target any of the cannabinoid receptors overexpressed in glioma cells, we decorated the LNCs with CBD. This functionalization strategy enhanced the in vitro glioma targeting by 3.4-fold in comparison with their equally-sized undecorated counterparts. Lastly, the combination of CBD-loading with CBD-functionalization further reduced the IC50 values. Hence, the potential of these two strategies of CBD incorporation into LNCs deserves subsequent in vivo evaluation.
dc.description.departmentDepto. de Farmacia Galénica y Tecnología Alimentaria
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad Complutense de Madrid
dc.description.sponsorshipBanco Santander
dc.description.sponsorshipMinisterio de Educación, Cultura y Deporte(España)
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.statuspub
dc.identifier.doi10.1016/j.ejpb.2018.11.020
dc.identifier.issn0939-6411
dc.identifier.officialurlhttps://doi.org/10.1016/j.ejpb.2018.11.020
dc.identifier.urihttps://hdl.handle.net/20.500.14352/97116
dc.journal.titleEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.language.isoeng
dc.page.final137
dc.page.initial126
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/FPU13/02325
dc.relation.projectIDinfo:eu-repo/grantAgreement/EST14/00229
dc.rights.accessRightsrestricted access
dc.subject.keywordCannabinoids
dc.subject.keywordCannabinoids
dc.subject.keywordGlioma targeting
dc.subject.keywordExtended-release
dc.subject.keywordGlioblastoma
dc.subject.ucmTecnología farmaceútica
dc.subject.unesco3209.08 Preparación de Medicamentos
dc.titleLipid nanocapsules decorated and loaded with cannabidiol as targeted prolonged release carriers for glioma therapy: In vitro screening of critical parameters
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number134
dspace.entity.typePublication
relation.isAuthorOfPublication4cb1a1cd-ad04-41d8-b28d-ed9b8dde4d92
relation.isAuthorOfPublicationa7294851-3d9d-4fc2-98cc-80bf8b256236
relation.isAuthorOfPublication.latestForDiscovery4cb1a1cd-ad04-41d8-b28d-ed9b8dde4d92

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