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Please use this identifier to cite or link to this item: https://hdl.handle.net/11055/870
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dc.contributor.authorCheung LCen_US
dc.contributor.authorNguyen Men_US
dc.contributor.authorTang Een_US
dc.contributor.authorvon Ungern Sternbeg BSen_US
dc.contributor.authorSalman Sen_US
dc.contributor.authorTuleu Cen_US
dc.contributor.authorMohamed Ahmed AHAen_US
dc.contributor.authorSoto Jen_US
dc.contributor.authorLim LYen_US
dc.date2017-11-11-
dc.date.accessioned2019-08-05T05:33:35Z-
dc.date.available2019-08-05T05:33:35Z-
dc.identifier.citation535(1-2):194-200en_US
dc.identifier.urihttp://hdl.handle.net/11055/870-
dc.description.abstractHarmonized methodologies are urgently required for the taste evaluation of novel pediatric medicines. This study utilized in vitro, in vivo and clinical data to evaluate the palatability of a novel midazolam chocolate tablet. In vitro dissolution experiments showed the crushed tablet to release within 5 min 1.68 mg of midazolam into simulated saliva. This translated to a drug level of 0.84 mg/ml in the oral cavity, which would be higher than the midazolam bitterness detection threshold concentration of 0.03 mg/ml determined in a rat 'brief access taste aversion' (BATA) model. The visual analogue scale scores of patients aged 4-16 years prescribed with midazolam pre-surgery showed a clear preference for the midazolam chocolate tablets (3.35 ± 1.04, n = 20) compared to the control midazolam solution (1.47 ± 0.62, n = 17). The clinical data was in agreement with the in vivo rodent data in showing the novel chocolate tablet matrix to be effective at taste-masking the bitter midazolam.en_US
dc.subjectAdolescenten_US
dc.subjectChilden_US
dc.subjectDrug Compoundingen_US
dc.subjectDrug Liberationen_US
dc.subjectFeeding Behavior/drug effectsen_US
dc.subjectFlavoring Agents/chemistryen_US
dc.subjectMidazolam/administration & dosageen_US
dc.subjectMidazolam/chemistryen_US
dc.subjectTaste Perception/drug effectsen_US
dc.titleTaste evaluation of a novel midazolam tablet for pediatric patients: In vitro drug dissolution, in vivo animal taste aversion and clinical taste perception profiles.en_US
dc.typeJournal Articleen_US
dc.type.contentTexten_US
dc.identifier.journaltitleInternational Journal of Pharmaceuticsen_US
dc.identifier.doi10.1016/j.ijpharm.2017.10.060en_US
dc.description.affiliatesPrincess Margaret Hospital for Childrenen_US
dc.description.affiliatesUniversity of Western Australiaen_US
dc.description.affiliatesQEII Medical Centreen_US
dc.description.affiliatesUniversity College Londonen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/29104056en_US
dc.type.studyortrialRandomized Controlled Clinical Trial/Controlled Clinical Trialen_US
dc.ispartof.anzcaresearchfoundationYesen_US
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:Scholarly and Clinical
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