Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/105904
DC FieldValue
dc.titleEffects of poly(vinylpyrrolidone) and ethylcellulose on alginate microspheres prepared by emulsification
dc.contributor.authorChan, L.W.
dc.contributor.authorHeng, P.W.S.
dc.date.accessioned2014-10-29T01:52:15Z
dc.date.available2014-10-29T01:52:15Z
dc.date.issued1998
dc.identifier.citationChan, L.W., Heng, P.W.S. (1998). Effects of poly(vinylpyrrolidone) and ethylcellulose on alginate microspheres prepared by emulsification. Journal of Microencapsulation 15 (4) : 409-420. ScholarBank@NUS Repository.
dc.identifier.issn02652048
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/105904
dc.description.abstractCalcium alginate microspheres were prepared by an emulsification process. The effects of two co-polymers, namely poly(vinylpyrrolidone) and ethylcellulose, on the properties of the microspheres were studied. Microspheres prepared with and without poly(vinylpyrrolidone) were spherical and discrete. The microspheres containing poly(vinylpyrrolidone) exhibited a better flow property but the drug content was lower and the drug release rate higher. The method of incorporating poly(vinylpyrrolidone) was found to (significantly) affect the size distribution and drug content of the microspheres. Ethylcellulose produced marked aggregation of the microspheres which also showed a lower drug content, but a slower drug release. The retardation in drug release was attributed to the formation of aggregated microspheres with a less permeable matrix. The addition of triethyl citrate, which is a water-soluble plasticizer, was found to increase the rate of drug release while the use of a higher viscosity grade of ethylcellulose produced the opposite effect. Ethylcellulose improved the flowability of the microspheres to a greater extent than poly(vinylpyrrolidone).
dc.sourceScopus
dc.subjectAlginate
dc.subjectDrug release
dc.subjectEthylcellulose
dc.subjectMicrospheres
dc.subjectPoly(vinylpyrrolidone)
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.sourcetitleJournal of Microencapsulation
dc.description.volume15
dc.description.issue4
dc.description.page409-420
dc.description.codenJOMIE
dc.identifier.isiutNOT_IN_WOS
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