Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/4855
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChadha, Renu-
dc.contributor.authorKapoor, V K-
dc.contributor.authorKumar, Amit-
dc.date.accessioned2009-06-26T05:34:36Z-
dc.date.available2009-06-26T05:34:36Z-
dc.date.issued2006-06-
dc.identifier.issn0975-1084 (Online); 0022-4456 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/4855-
dc.description459-469en_US
dc.description.abstractHomogeneous distribution of poorly water-soluble drugs in polyvinylpyrrolidone (PVP), a hydrophilic carrier, is definitely a suitable way to improve the bioavailability of such drugs. However, fundamental knowledge of drug polymer interaction and comprehensive study of the thermal, structural and solubility properties of such binary systems is the prerequisite for the development of useful drug product. The paper reviews physical state, dissolution behavior and elucidation of drug-PVP interaction in solid dispersion using XRD, FTIR, DSC, SEM, hot stage microscopy and NMR. The importance of suitable selection of the system preparation methods have also been demonstrated and emphasis is laid on the potential methods for the industrial production of solid dispersions.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesA61J3/07en_US
dc.sourceJSIR Vol.65(06) [June 2006]en_US
dc.subjectDSCen_US
dc.subjectFTIRen_US
dc.subjectPolyvinylpyrrolidoneen_US
dc.subjectSolid dispersionen_US
dc.subjectSolubilityen_US
dc.subjectX-Ray diffractionen_US
dc.titleAnalytical techniques used to characterize drug-polyvinylpyrrolidone systems in solid and liquid states – An overviewen_US
dc.typeArticleen_US
Appears in Collections:JSIR Vol.65(06) [June 2006]

Files in This Item:
File Description SizeFormat 
JSIR 65(6) 459-469.pdf116.48 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.