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dc.contributor.authorOmrani, Sondes
dc.contributor.authorGamoudi, Safa
dc.contributor.authorViseras Alarcón, César 
dc.contributor.authorMoussaoui, Younes
dc.contributor.authorSainz Díaz, C. Ignacio
dc.date.accessioned2024-11-03T21:08:15Z
dc.date.available2024-11-03T21:08:15Z
dc.date.issued2024-09-28
dc.identifier.citationSondes, O. et. al. Molecules 2024, 29(19), 4612; [https://doi.org/10.3390/molecules29194612]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/96554
dc.description.abstractThis work combines experimental and computational modeling studies for the preparation of a composite of metformin and an organoclay, examining the advantages of a Tunisian clay used for drug delivery applications. The clay mineral studied is a montmorillonite-like smectite (Sm-Na), and the organoclay derivative (HDTMA-Sm) was used as a drug carrier for metformin hydrochloride (MET). In order to assess the MET loading into the clays, these materials were characterized by means of cation exchange capacity assessment, specific surface area measurement, and with the techniques of X-ray diffraction (XRD), differential scanning calorimetry, X-ray fluorescence spectroscopy, and Fourier-transformed infrared spectroscopy. Computational molecular modeling studies showed the surface adsorption process, identifying the clay–drug interactions through hydrogen bonds, and assessing electrostatic interactions for the hybrid MET/Sm-Na and hydrophobic interactions and cation exchange for the hybrid MET/HDTMA-Sm. The results show that the clays (Sm-Na and HDTMA-Sm) are capable of adsorbing MET, reaching a maximum load of 12.42 and 21.97 %, respectively. The adsorption isotherms were fitted by the Freundlich model, indicating heterogeneous adsorption of the studied adsorbate–adsorbent system, and they followed pseudo-second-order kinetics. The calculations of ΔGº indicate the spontaneous and reversible nature of the adsorption. The calculation of ΔH° indicates physical adsorption for the purified clay (Sm-Na) and chemical adsorption for the modified clay (HDTMA-Sm). The release of intercalated MET was studied in media simulating gastric and intestinal fluids, revealing that the purified clay (Sm-Na) and the modified organoclay (HDTMA-Sm) can be used as carriers in controlled drug delivery in future clinical applications. The molecular modeling studies confirmed the experimental phenomena, showing that the main adsorption mechanism is the cation exchange process between proton and MET cations into the interlayer space.es_ES
dc.description.sponsorshipAndalusian Government (project P18-RT-3786), Spanish Science and Innovation Ministry (project PID2022-137603OB-I00)es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectmetformines_ES
dc.subjectclay mineralses_ES
dc.subjectsmectitees_ES
dc.subjectmolecular modelinges_ES
dc.titleThe Use of Organoclays as Excipient for Metformin Delivery: Experimental and Computational Studyes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/molecules29194612
dc.type.hasVersionVoRes_ES


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