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dc.relation.isnodouble4e09a89d-148a-4572-a5de-a38ae88a04ab*
dc.relation.isnodouble04555008-ad8c-4047-bf2b-956d33dfdbf0*
dc.relation.isnodouble7fb6c54c-7ffb-4ef1-bf5d-06300ab6cf60*
dc.relation.isnodouble707176c1-1f25-4c5b-9b5f-47e89fa2a3c6*
hal.structure.identifierInstitut de Mécanique et d'Ingénierie [I2M]
dc.contributor.authorDESBOIS, Léo
hal.structure.identifierInstitut de Mécanique et d'Ingénierie [I2M]
dc.contributor.authorTCHORELOFF, Pierre
IDREF: 069233624
hal.structure.identifierUniversité de Bordeaux [UB]
hal.structure.identifierInstitut de Mécanique et d'Ingénierie [I2M]
dc.contributor.authorMAZEL, Vincent
IDREF: 113057954
dc.date.accessioned2021-05-14T09:30:35Z
dc.date.available2021-05-14T09:30:35Z
dc.date.issued2020-09
dc.identifier.issn0378-5173
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/75823
dc.description.abstractEnEvolution of the compaction properties of powders with the compaction speed (strain rate sensitivity, SRS) is a common phenomenon during the manufacturing of pharmaceutical tablets. Nevertheless, several different phenomena can be responsible of the SRS like friction, viscoelasticity, viscoplasticity or air entrapment.In this work, an original experimental methodology was developed to characterize specifically the viscoelasticity of tablets using a compaction simulator. After various compressions, tablets were finally loaded elastically at different constant strain rates. This methodology made it possible to measure the apparent bulk and shear moduli as a function of the strain rate. The methodology was successfully applied to microcrystalline cellulose (MCC), Starch, Lactose monohydrate (GLac) and Anhydrous Calcium Phosphate (ACP). No significant evolution of the moduli was found for Lac and ACP as expected. On the contrary, for MCC and Starch, both shear and bulk moduli were found to increase along with the strain rate. The viscoelastic behavior was then successfully modeled using prony series. Assessment of the model parameters was achieved by inverse identification using an analytical model and a finite element analysis.
dc.description.sponsorshipClivage en compression pharmaceutique - ANR-17-CE08-0015
dc.language.isoen
dc.publisherElsevier
dc.subject.enViscoelasticity
dc.subject.enCompaction
dc.subject.enSpeed
dc.subject.enStrain rate sensitivity
dc.subject.enMechanical behavior
dc.subject.enTablet
dc.title.enCharacterization and modeling of the viscoelasticity of pharmaceutical tablets
dc.typeArticle de revue
dc.identifier.doi10.1016/j.ijpharm.2020.119695
dc.subject.halSciences de l'ingénieur [physics]
bordeaux.journalInternational Journal of Pharmaceutics
bordeaux.page1-7
bordeaux.volume587
bordeaux.hal.laboratoriesInstitut de Mécanique et d’Ingénierie de Bordeaux (I2M) - UMR 5295*
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
bordeaux.institutionCNRS
bordeaux.institutionINRAE
bordeaux.institutionArts et Métiers
bordeaux.peerReviewedoui
hal.identifierhal-03166915
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-03166915v1
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