Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/41407
Registro completo de metadatos
Campo DC Valor Lengua/Idioma
dc.contributor.authorRomán Vargas, Yoreny-
dc.contributor.authorBlandón Naranjo, Lucas Hernán-
dc.contributor.authorBenjumea Gutiérrez, Dora María-
dc.contributor.authorPérez Pérez, León Darío-
dc.contributor.authorPorras Arguello, Julián David-
dc.date.accessioned2024-08-25T15:05:33Z-
dc.date.available2024-08-25T15:05:33Z-
dc.date.issued2023-
dc.identifier.citationRomán-Vargas, Y.; Porras-Arguello, J.D.; BlandónNaranjo, L.; Pérez-Pérez, L.D.; Benjumea, D.M. Evaluation of the Analgesic Effect of High-CannabidiolContent Cannabis Extracts in Different Pain Models by Using Polymeric Micelles as Vehicles. Molecules 2023, 28, 4299. https://doi.org/10.3390/molecules28114299spa
dc.identifier.urihttps://hdl.handle.net/10495/41407-
dc.description.abstractABSTRACT: Currently, cannabis is considered an attractive option for the treatment of various diseases, including pain management. Thus, developing new analgesics is paramount for improving the health of people suffering from chronic pain. Safer natural derivatives such as cannabidiol (CBD) have shown excellent potential for the treatment of these diseases. This study aimed to evaluate the analgesic effect of a CBD-rich cannabis extract (CE) encapsulated in polymeric micelles (CBD/PMs) using different pain models. The PEG-PCL polymers were characterized by gel permeation chromatography and 1H-NMR spectroscopy. PMs were prepared by solvent evaporation and characterized by dynamic light scattering (DLS) and transmission electron microscopy. The analgesic activity of CBD/PMs and nonencapsulated CE rich in CBD (CE/CBD) was evaluated using mouse thermal, chemical, and mechanical pain models. The acute toxicity of the encapsulated CE was determined by oral administration in mice at a dose of 20 mg/kg for 14 days. The release of CBD from the nanoparticles was assessed in vitro using a dialysis experiment. CBD/PMs with an average hydrodynamic diameter of 63.8 nm obtained from a biocompatible polyethylene glycol-block-polycaprolactone copolymer were used as nanocarriers for the extract formulations with 9.2% CBD content, which corresponded with a high encapsulation efficiency of 99.9%. The results of the pharmacological assays indicated that orally administered CBD/PMs were safe and exerted a better analgesic effect than CE/CBD. The micelle formulation had a significant analgesic effect in a chemical pain model, reaching a percentage of analgesia of 42%. CE was successfully encapsulated in a nanocarrier, providing better stability. Moreover, it proved to be more efficient as a carrier for CBD release. The analgesic activity of CBD/PMs was higher than that of free CE, implying that encapsulation is an efficient strategy for improving stability and functionality. In conclusion, CBD/PMs could be promising therapeutics for pain management in the future.spa
dc.format.extent17 páginasspa
dc.format.mimetypeapplication/pdf - application/epubspa
dc.language.isoengspa
dc.publisherMDPIspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleEvaluation of the analgesic effect of high-cannabidiol-content cannabis extracts in different pain models by using polymeric micelles as vehiclesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo Interdisciplinario de Estudios Molecularesspa
dc.publisher.groupToxinología, Alternativas Terapéuticas y Alimentariasspa
dc.identifier.doi10.3390/molecules28114299-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1420-3049-
oaire.citationtitleMoleculesspa
oaire.citationstartpage1spa
oaire.citationendpage17spa
oaire.citationvolume28spa
oaire.citationissue11spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
oaire.fundernameColombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasspa
dc.publisher.placeBasilea, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsAnalgésicos - farmacología-
dc.subject.decsAnalgesics - pharmacology-
dc.subject.decsAnalgésicos - uso terapéutico-
dc.subject.decsAnalgesics - therapeutic use-
dc.subject.decsCannabidiol - farmacología-
dc.subject.decsCannabidiol - pharmacology-
dc.subject.decsCannabidiol - uso terapéutico-
dc.subject.decsCannabidiol - therapeutic use-
dc.subject.decsAgonistas de Receptores de Cannabinoides-
dc.subject.decsCannabinoid Receptor Agonists-
dc.subject.decsCannabis-
dc.subject.decsDolor Crónico - tratamiento farmacológico-
dc.subject.decsChronic Pain - drug therapy-
dc.subject.decsAlucinógenos-
dc.subject.decsHallucinogens-
dc.subject.decsRatones-
dc.subject.decsMice-
dc.subject.decsMicelas-
dc.subject.decsMicelles-
dc.subject.decsExtractos Vegetales - farmacología-
dc.subject.decsPlant Extracts - pharmacology-
dc.subject.decsPolímeros - química-
dc.subject.decsPolymers - chemistry-
dc.subject.decsDiálisis Renal-
dc.subject.decsRenal Dialysis-
dc.description.researchgroupidCOL0014476spa
dc.description.researchgroupidCOL0007462spa
oaire.awardnumberMinCiencias 63013spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000700-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D002185-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D063386-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D002188-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D059350-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D006213-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D051379-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008823-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D010936-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D011108-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D006435-
dc.relation.ispartofjournalabbrevMoleculesspa
oaire.funderidentifier.rorRoR:03fd5ne08-
Aparece en las colecciones: Artículos de Revista en Farmacéutica y Alimentarias

Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
RomanYoreny_2023_Evaluation_Analgesic_Effect.epubArtículo de investigación2.89 MBEPUBVisualizar/Abrir
RomanYoreny_2023_Evaluation_Analgesic_Effect.pdfArtículo de investigación1.93 MBAdobe PDFVisualizar/Abrir


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons