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dc.contributor.authorKarlsen, Iselin
dc.contributor.authorSkalko-Basnet, Natasa
dc.contributor.authorHolsæter, Ann Mari
dc.date.accessioned2023-09-08T08:12:22Z
dc.date.available2023-09-08T08:12:22Z
dc.date.issued2019
dc.description.abstract<p>Docetaxel (DOC) is a potent anticancer drug with several limitations, including poor solubility and the reported serious side effects, attributed to either the drug itself or the solvent used. Thus, it is interesting to entrap the drug into liposomes in order to solubilize the drug and improve the therapeutic outcome. <p>The fist aim of this study was to establish a small-scale screening method for preparing and characterizing DOC-liposomes. Secondly, the established methods were applied to investigate the effect of lipid composition on the liposomal drug entrapment.en_US
dc.identifier.cristinIDFRIDAID 1659349
dc.identifier.urihttps://hdl.handle.net/10037/30795
dc.language.isoengen_US
dc.titleDocetaxel Liposomes - A formulation Screening Studyen_US
dc.typeConference objecten_US
dc.typeKonferansebidragen_US


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