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dc.contributor.authorKocabaş, Nazife Özge
dc.contributor.authorKahraman Şirin, Emine
dc.contributor.authorGüngör, Sevgi
dc.date.accessioned2021-12-10T10:55:05Z
dc.date.available2021-12-10T10:55:05Z
dc.identifier.citationKocabaş N. Ö. , Kahraman Şirin E., Güngör S., "Assessment of membrane type effects on in vitro performance of topical semi-solid products", Journal Of Drug Delivery Science And Technology, cilt.64, ss.1-8, 2021
dc.identifier.issn1773-2247
dc.identifier.othervv_1032021
dc.identifier.otherav_5c1e6956-3c20-427d-b32b-bf757d15a578
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170839
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1773224721003269?dgcid=author
dc.identifier.urihttps://doi.org/10.1016/j.jddst.2021.102646
dc.description.abstractIn vitrorelease tests have been widely used to assess performance of topical products. Any interaction should not be observed between drug and synthetic membrane, but there is no conclusive information about relationship of membrane type and properties of drug substances. In this study, four types of membranes (regenerated cellulose,cellulose acetate, mixed cellulose ester, silicone) were used to evaluatein vitrorelease of hydrophilic, moderately lipophilic and highly lipophilic drug substances from their topical preparations. The relationship between membrane type and drug characteristics was investigated using Strat-M™ membrane resembling to human skin, and excised porcine skin forin vitropermeation studies. The release data revealed that acceptor/donor groups in drug substance and synthetic membrane could hinder drug release through membrane. Mixed cellulose ester or cellulose acetate membranes should be opted forin vitrorelease studies of drugs consisting of abundant, strong acceptor/donor groups.In vitropermeation data showed that druglipophilicitymight come into prominence for these studies. Strat-M™ membrane could be more useful to estimate permeability of lipophilic molecules rather than hydrophilic ones. The results suggest that molecular structure and lipophilicity of drug could be considered to select synthetic membrane used forin vitrorelease and permeation studies.
dc.language.isoeng
dc.subjectPharmacology, Toxicology and Pharmaceutics (miscellaneous)
dc.subjectLife Sciences
dc.subjectEczacılık
dc.subjectSağlık Bilimleri
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp (MED)
dc.titleAssessment of membrane type effects on in vitro performance of topical semi-solid products
dc.typeMakale
dc.relation.journalJournal Of Drug Delivery Science And Technology
dc.contributor.departmentİstanbul Üniversitesi , Eczacılık Fakültesi , Eczacılık Teknolojisi Bölümü
dc.identifier.volume64
dc.identifier.startpage1
dc.identifier.endpage8
dc.contributor.firstauthorID2645364


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