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dc.contributor.authorPedrosa Bustos, María 
dc.contributor.authorMaldonado Valderrama, Julia 
dc.contributor.authorGálvez Ruiz, María José 
dc.date.accessioned2022-07-15T07:27:01Z
dc.date.available2022-07-15T07:27:01Z
dc.date.issued2022-03-27
dc.identifier.citationPedrosa, M., Maldonado-Valderrama, J., & Gálvez-Ruiz, M. J. (2022). Interactions between curcumin and cell membrane models by Langmuir monolayers. Colloids and Surfaces B: Biointerfaces, 217, 112636es_ES
dc.identifier.urihttp://hdl.handle.net/10481/76025
dc.description.abstractStudying interactions between potential anticancer drugs and cell membrane models is of great interest to explore the capability of novel drugs in the development of anticancer treatments. Lipid membrane models are useful to understand cellular interactions and to discern drug mechanism action. Here, the interactions of curcumin, as a bioactive natural compound with anti-cancer properties, with both healthy and cancerous or tumor cell membrane models, based on Langmuir monolayers, have been studied. The healthy-cell membrane model is composed of cholesterol 67%, and saturated lipid dipalmitoylphosphatidylcholine 33%. The cancerous-cell-membrane-model is composed of a lower proportion of cholesterol, 25%, and unsaturated lipid sphingomyelin 75%. To compare their interaction with curcumin we report the compression isotherms registered for both lipid membrane models and curcumin in different proportions, their compression moduli and the thermodynamic interaction parameters. From this analysis, we evidence a destabilizing interaction between curcumin and the cancerous cell membrane model in comparison with the healthy one. This interaction is further visualized by micro-Brewster Angle and Atomic Force Microscopies. Our experiments show that the drug enhances cohesion in the healthy membrane model whereas it fluidifies the cancerous cell membrane model causing thermodynamic destabilization. These are useful results to improve the selectivity of the drug avoiding adverse side effects of most current anticancer therapies.es_ES
dc.description.sponsorshipThis work has been supported by project RTI2018-101309-B-C21 funded by MCIN/AEI/10.13039/501100011033/FEDER. María Pedrosa Bustos thanks the FPU19/02045 fellowship funded by MCIN/AEI/10.13039/501100011033 and FSE. This work has been done in the framework of the doctoral of AAG in the Doctoral Programme in Physics and Space Sciences (B09/56/1) of the University of Granada. JMV acknowledges support from project PID2020-116615RA-I00 funded by MCIN/ AEI /10.13039/501100011033. This work was also partially supported by the Biocolloid and Fluid Physics Group (ref. PAI-FQM115) of the University of Granada (Spain). Funding for open access charge: Universidad de Granada / CBUA.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMonolayeres_ES
dc.subjectMonocapases_ES
dc.subjectCell membranes es_ES
dc.subjectMembrana celulares_ES
dc.subjectMembranas celulareses_ES
dc.subjectCurcumines_ES
dc.subjectCurcuminaes_ES
dc.subjectLangmuir monolayerses_ES
dc.subjectMonocapas de Langmuires_ES
dc.subjectMicro BAMes_ES
dc.subjectBrewster Angle Microscopyes_ES
dc.subjectAFMes_ES
dc.subjectAtomic force microscopyes_ES
dc.subjectMicroscopio de fuerza atómicaes_ES
dc.subjectDPPCes_ES
dc.subjectEsfingomielinaes_ES
dc.subjectSphingomyelines_ES
dc.titleInteractions between curcumin and cell membrane models by Langmuir monolayerses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1016/j.colsurfb.2022.112636


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional