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dc.contributor.authorAzarmi, S
dc.contributor.authorRoa, W
dc.contributor.authorLobenberg, R
dc.date.accessioned2018-08-26T08:29:22Z
dc.date.available2018-08-26T08:29:22Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51768
dc.description.abstractThe purpose of this article is to review USP and non-pharmacopcial dissolution testing methods for conventional and novel pharmaceutical dosage forms and give an insight to possible alternatives in drug dissolution study design and appropriate choices for dissolution media. For each dosage form first the USP method(s) for dissolution testing are reviewed followed by alternative methods used in research and development. (c) 2006 Elsevier B.V. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofINTERNATIONAL JOURNAL OF PHARMACEUTICS
dc.subjectdissolution testing
dc.subjectUSP
dc.subjectnovel dosage forms
dc.subjectconventional dosage forms
dc.subjectimmediate-release tablets
dc.subjectpowders
dc.subjectextended-release
dc.subjectchewable tablets
dc.subjectbuccal/sublingual tablets
dc.subjectchewing gums
dc.subjectsoft gelatin capsules
dc.subjectsuppositories
dc.subjecttransdermal patches
dc.subjectsemisolids
dc.subjectaerosols
dc.titleCurrent perspectives in dissolution testing of conventional and novel dosage forms
dc.typeReview
dc.citation.volume328
dc.citation.issue1
dc.citation.spage12
dc.citation.epage21
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.ijpharm.2006.10.001


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