Formulation of Sustained Release Hydrophilic Matrix Tablets of Tolcapone with the Application of Sedem Diagram: Influence of Tolcapone's Particle Size on Sustained Release

dc.contributor.authorNardi Ricart, Anna
dc.contributor.authorNofrerias Roig, Isaac
dc.contributor.authorSuñé Pou, Marc
dc.contributor.authorPérez Lozano, Pilar
dc.contributor.authorMiñarro Carmona, Montserrat
dc.contributor.authorGarcía Montoya, Encarna
dc.contributor.authorTicó Grau, Josep R.
dc.contributor.authorInsa Boronat, Raul
dc.contributor.authorSuñé i Negre, Josep M. (Josep Maria)
dc.date.accessioned2021-02-03T14:12:13Z
dc.date.available2021-02-03T14:12:13Z
dc.date.issued2020-07-01
dc.date.updated2021-02-03T14:12:13Z
dc.description.abstractHydrophilic matrix tablets are a type of sustained release dosage form characterized by distributing a drug in a matrix that is usually polymeric. Tolcapone is a drug that inhibits the enzyme catechol-O-methyl transferase. In recent years, it has been shown that tolcapone is a potent inhibitor of the amyloid aggregation process of the transthyretin protein, and acts by stabilizing the structure of the protein, reducing the progression of familial amyloid polyneuropathy. The main objective of this study was to obtain a sustained release tablet of tolcapone for oral administration with a preferred dosage regimen of 1 administration every 12 or 24 h and manufactured, preferably, by direct compression. The SeDeM Diagram method has been used for the formulation development of hydrophilic matrix tablets. Given the characteristics of tolcapone, the excipient selected for the formation of the polymeric matrix was a high viscosity hydroxypropylmethylcellulose (Methocel® K100M CR). A decrease in the particle size of tolcapone resulted in a slower dissolution release of the formulation when the concentration of the polymer Methocel® K100M CR was below 29%. These surprising and novel results have given rise to patent number WO/2018/019997.
dc.format.extent18 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec704242
dc.identifier.issn1999-4923
dc.identifier.pmid32708961
dc.identifier.urihttps://hdl.handle.net/2445/173623
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/pharmaceutics12070674
dc.relation.ispartofPharmaceutics, 2020, vol. 12, num. 7
dc.relation.urihttps://doi.org/10.3390/pharmaceutics12070674
dc.rightscc-by (c) Nardi Ricart, Anna et al., 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
dc.subject.classificationInhibidors enzimàtics
dc.subject.classificationAmiloïdosi
dc.subject.classificationMalaltia de Parkinson
dc.subject.otherEnzyme inhibitors
dc.subject.otherAmyloidosis
dc.subject.otherParkinson's disease
dc.titleFormulation of Sustained Release Hydrophilic Matrix Tablets of Tolcapone with the Application of Sedem Diagram: Influence of Tolcapone's Particle Size on Sustained Release
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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