Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/12480
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dc.contributor.authorKapor A.en
dc.contributor.authorManojlović Nikolić, V.en
dc.contributor.authorNikolić L.en
dc.contributor.authorStanković M.en
dc.contributor.authorCakić M.en
dc.contributor.authorStanojević L.en
dc.contributor.authorIlić D.en
dc.date.accessioned2020-03-03T14:48:38Z-
dc.date.available2020-03-03T14:48:38Z-
dc.date.issued2010-08-01en
dc.identifier.issn18951066en
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/12480-
dc.description.abstractIn this paper the procedure for the preparation of inclusion complexes of amlodipine besylate with β-cyclodextrin (β-CD) and 2-hydrohypropyl-β-cyclodextrin (HPβ-CD) and their structural characterization was described. Molecular inclusion complexes of amlodipine besylate are prepared by the coprecipitation method and characterised by the application of spectroscopic methods FTIR, 1H-NMR and XRD. The photosensitivity of amlodipine besylate in the inclusion complexes was also determined with respect to uncomplexed agent. DSC curves indicate the loss of the clear peak due to melting of amlodipine besylate at about 200°C, while on XR diffractograms certain reflections are lost belonging to amlodipine besylate in complexes. This indicates its inclusion in the vacancies of the host. The inclusion of amlodipine besylate with cyclodextrins increases the stability, i.e. decreases the photosensitivity of amlodipine besylate. © 2010 Versita Warsaw and Springer-Verlag Wien.en
dc.relation.ispartofCentral European Journal of Chemistryen
dc.titleInclusion complexes of amlodipine besylate and cyclodextrinsen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.2478/s11532-010-0061-8en
dc.identifier.scopus2-s2.0-77953908940en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/77953908940en
dc.relation.lastpage841en
dc.relation.firstpage834en
dc.relation.issue4en
dc.relation.volume8en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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