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dc.contributor.authorValizadeh, H
dc.contributor.authorZakeri-Milani, P
dc.contributor.authorBarzegar-Jalali, M
dc.contributor.authorMohammadi, G
dc.contributor.authorDanesh-Bahreini, MA
dc.contributor.authorAdibkia, K
dc.contributor.authorNokhodchi, A
dc.date.accessioned2018-08-26T06:33:56Z
dc.date.available2018-08-26T06:33:56Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43863
dc.description.abstractThe objective of this study was to improve the dissolution rate of a poor water soluble drug, piroxicam, by solid dispersion technique. Solid dispersions were prepared by three different methods depending on the type of carrier. The dissolution rate of piroxicam was markedly increased in solid dispersion of myrj 52, Eudragit E100 and mannitol. Solubility studies revealed a marked increase in the solubility of piroxicam with an increase in myrj 52 and Eudragit E100 concentrations. Data from the X-ray diffraction and FT-IR spectroscopy showed that piroxicam was amorphous in the solid dispersions prepared with dextrin and Eudragit E100.
dc.language.isoEnglish
dc.relation.ispartofDrug development and industrial pharmacy
dc.subjectAcrylates
dc.subjectDrug Carriers
dc.subjectHydrogen-Ion Concentration
dc.subjectPiroxicam
dc.subjectPolymers
dc.subjectSolubility
dc.subjectSpectroscopy, Fourier Transform Infrared
dc.subjectX-Ray Diffraction
dc.titlePreparation and characterization of solid dispersions of piroxicam with hydrophilic carriers.
dc.typearticle
dc.citation.volume33
dc.citation.issue1
dc.citation.spage45
dc.citation.epage56
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1080/03639040600814965


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