نمایش پرونده ساده آیتم

dc.contributor.authorSoltani, N
dc.contributor.authorShaynafar, A
dc.contributor.authorDjozan, D
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T09:35:45Z
dc.date.available2018-08-26T09:35:45Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57910
dc.description.abstractCosolvency and complex formation are the important methods to increase the solubility of drugs. These methods can be used to change solubility simultaneously. In this study, solubilities of three basic drugs, i.e. atenolol, diazepam and lamotrigine, were studied in binary mixtures of propylene glycol + water in the presence of cyclodextrin (CD) and atenolol in this solvent mixture in the absence of CD using saturating shake flask method. The generated solubility data was fitted to the Jouyban-Acree model and the solubility profile of each drug was compared with solubility data in the absence of CD that the solubility data of diazepam and lamotrigine taken from the literature.
dc.language.isoEnglish
dc.relation.ispartofJournal of Drug Delivery Science and Technology
dc.subjectatenolol
dc.subjectbeta cyclodextrin
dc.subjectcyclodextrin
dc.subjectdiazepam
dc.subjectlamotrigine
dc.subjectpropylene glycol
dc.subjectarticle
dc.subjectdissociation constant
dc.subjectdrug delivery system
dc.subjectdrug solubility
dc.subjectreproducibility
dc.titleSolubility of three basic drugs in propylene glycol + water mixtures in the presence of ?-cyclodextrin
dc.typeArticle
dc.citation.volume23
dc.citation.issue2
dc.citation.spage187
dc.citation.epage190
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1016/S1773-2247(13)50028-1


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم