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Studium vlivu hydrofilního nosiče na rychlost rozpouštění léčiva ze skupiny BCSII
dc.contributor.advisorŠklubalová, Zdeňka
dc.creatorBunes, Andrea Suther
dc.date.accessioned2021-06-24T09:31:29Z
dc.date.available2021-06-24T09:31:29Z
dc.date.issued2021
dc.identifier.urihttp://hdl.handle.net/20.500.11956/126378
dc.description.abstractCharles University, Faculty of Pharmacy in Hradci Králové Department of: Pharmaceutical Technology Supervisor: Assoc. Prof. PharmDr. Zdenka Šklubalová, Ph.D. Consultant: Mgr. Jana Brokešová Student: Andrea Suther Bunes Title of Thesis: Study of influence of hydrophilic carriers on the dissolution rate of a BCS II drug The aim of this thesis was to study the effect of mixing and co-milling with hydrophilic carriers on the dissolution rate of a model BCS II drug meloxicam. The mixtures of two different drug loads (1-1, 1-8) were characterized for granulometric and dissolution parameters. USP-4 apparatus assembled with a flow-through powder cell (an open loop) was used to estimate meloxicam relative dissolution rate rrel (min-1 ). Mixing with lactose, particularly in a higher ratio, increased the relative dissolution rate in comparison to the pure meloxicam. The effect was further increased by co-milling, but an unfavourable event of agglomeration occurred, especially for the 1-1 drug-excipient ratio sample. Adding chitosan solved this problem due to the formation of interactive mixture. The co-milled sample containing chitosan and lactose in a 1-8 ratio showed the highest rrel = 0.48 min-1 .en_US
dc.languageEnglishcs_CZ
dc.language.isoen_US
dc.publisherUniverzita Karlova, Farmaceutická fakulta v Hradci Královécs_CZ
dc.subjectcarrieren_US
dc.subjectsolubilityen_US
dc.subjectdissolutionen_US
dc.subjectmillingen_US
dc.subjectmixingen_US
dc.titleStudy of influence of a hydrophilic carrier on the dissolution rate of the BCS II drugen_US
dc.typediplomová prácecs_CZ
dcterms.created2021
dcterms.dateAccepted2021-06-01
dc.description.departmentDepartment of Pharmaceutical Technologyen_US
dc.description.departmentKatedra farmaceutické technologiecs_CZ
dc.description.facultyFaculty of Pharmacy in Hradec Královéen_US
dc.description.facultyFarmaceutická fakulta v Hradci Královécs_CZ
dc.identifier.repId218281
dc.title.translatedStudium vlivu hydrofilního nosiče na rychlost rozpouštění léčiva ze skupiny BCSIIcs_CZ
dc.contributor.refereeVraníková, Barbora
thesis.degree.nameMgr.
thesis.degree.levelmagisterskécs_CZ
thesis.degree.disciplineFarmaciecs_CZ
thesis.degree.disciplinePharmacyen_US
thesis.degree.programPharmacyen_US
thesis.degree.programFarmaciecs_CZ
uk.thesis.typediplomová prácecs_CZ
uk.taxonomy.organization-csFarmaceutická fakulta v Hradci Králové::Katedra farmaceutické technologiecs_CZ
uk.taxonomy.organization-enFaculty of Pharmacy in Hradec Králové::Department of Pharmaceutical Technologyen_US
uk.faculty-name.csFarmaceutická fakulta v Hradci Královécs_CZ
uk.faculty-name.enFaculty of Pharmacy in Hradec Královéen_US
uk.faculty-abbr.csFaFcs_CZ
uk.degree-discipline.csFarmaciecs_CZ
uk.degree-discipline.enPharmacyen_US
uk.degree-program.csFarmaciecs_CZ
uk.degree-program.enPharmacyen_US
thesis.grade.csVýborněcs_CZ
thesis.grade.enExcellenten_US
uk.abstract.enCharles University, Faculty of Pharmacy in Hradci Králové Department of: Pharmaceutical Technology Supervisor: Assoc. Prof. PharmDr. Zdenka Šklubalová, Ph.D. Consultant: Mgr. Jana Brokešová Student: Andrea Suther Bunes Title of Thesis: Study of influence of hydrophilic carriers on the dissolution rate of a BCS II drug The aim of this thesis was to study the effect of mixing and co-milling with hydrophilic carriers on the dissolution rate of a model BCS II drug meloxicam. The mixtures of two different drug loads (1-1, 1-8) were characterized for granulometric and dissolution parameters. USP-4 apparatus assembled with a flow-through powder cell (an open loop) was used to estimate meloxicam relative dissolution rate rrel (min-1 ). Mixing with lactose, particularly in a higher ratio, increased the relative dissolution rate in comparison to the pure meloxicam. The effect was further increased by co-milling, but an unfavourable event of agglomeration occurred, especially for the 1-1 drug-excipient ratio sample. Adding chitosan solved this problem due to the formation of interactive mixture. The co-milled sample containing chitosan and lactose in a 1-8 ratio showed the highest rrel = 0.48 min-1 .en_US
uk.file-availabilityV
uk.grantorUniverzita Karlova, Farmaceutická fakulta v Hradci Králové, Katedra farmaceutické technologiecs_CZ
thesis.grade.code1
dc.contributor.consultantBrokešová, Jana
uk.publication-placeHradec Královécs_CZ
uk.thesis.defenceStatusO


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