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dc.contributor.authorThomas, Felicity-
dc.date.accessioned2020-02-11T06:52:38Z-
dc.date.available2020-02-11T06:52:38Z-
dc.date.issued2019-
dc.identifier.issn1543-2521-
dc.identifier.issn2150-7376 (e)-
dc.identifier.otherBBKH680-
dc.identifier.urihttp://thuvienso.vanlanguni.edu.vn/handle/Vanlang_TV/15122-
dc.descriptionPharmaceutical Technology. Vol 43 (Octorber 2019)vi
dc.description.abstractIndustry is witnessing opportunities in novel drug discovery for the formulation of new NCEs in lipidbased drug delivery systems (LBDDS) so that bioavailability is improved." "Drug release is the important determinant to ensure maximum bioavailability at the site of action. [...]lipid formulations could be tailored to achieve desired drug-release kinetics by careful selection of lipid excipients." There may be issues as ratios of lipid components change from batch-tobatch. Because of these variables, it is recommended that drug developers work with experts who have extensive experience and knowledge of the development of LBDDS." [...]while the excipients used to construct lipid formulations are usually quite inert, many of these contain impurities, such as peroxides, aldehydes, or formic acid, that may trigger degradation pathways that are not seen when the same API is formulated in a solid formulation," specifies Speybroeck.vi
dc.language.isoenvi
dc.publisherMultiMedia Healthcare Inc.vi
dc.subjectPolyvinyl alcoholvi
dc.subjectLipidsvi
dc.subjectDrug delivery systemsvi
dc.subjectProduct developmentvi
dc.subjectDrug dosagesvi
dc.subjectBioavailabilityvi
dc.titleOvercoming Bioavailability 'Roadblocks' with LBDDSvi
dc.typeWorking Papervi
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