Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/105887
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dc.titleEffect of tabletting compaction pressure on alginate microspheres
dc.contributor.authorHeng P.W.S
dc.contributor.authorChan, L.W.
dc.contributor.authorLiew, C.V.
dc.contributor.authorNg, T.Y.
dc.date.accessioned2014-10-29T01:52:03Z
dc.date.available2014-10-29T01:52:03Z
dc.date.issued2000
dc.identifier.citationHeng P.W.S, Chan, L.W., Liew, C.V., Ng, T.Y. (2000). Effect of tabletting compaction pressure on alginate microspheres. Journal of Microencapsulation 17 (5) : 553-564. ScholarBank@NUS Repository.
dc.identifier.issn02652048
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/105887
dc.description.abstractAlginate and alginate-hydroxypropylmethylcellulose (HPMC) microspheres were prepared by the emulsification method. The compaction of microspheres for producing tablet dosage forms raises concerns about possible damage to microsphere walls with subsequent unpredictable dissolution rates. The effect of different compaction pressures on the integrity of the microspheres was investigated. The addition of a diluent, microcrystalline cellulose (MCC), was required to make compacts containing alginate and alginate-HPMC microspheres. Compacts containing alginate-HPMC (7:3) microspheres had the highest crushing strength followed by compacts containing alginate-HPMC (9:1) microspheres and alginate microspheres. However, compact crushing strength did not vary significantly with increased compaction pressures over the range of compaction pressures investigated. Differences in the drug release profiles of the original non-compacted and compacted alginate and alginate-HPMC microspheres were slight and not marked. Although dentation and distortion of the microspheres were observed with increasing compaction pressures, the microspheres generally remained intact, with minimal rupture/fracture.
dc.sourceScopus
dc.subjectAlginate
dc.subjectCompaction
dc.subjectHydroxypropylmethylcellulose
dc.subjectMicrospheres
dc.subjectTablet
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.sourcetitleJournal of Microencapsulation
dc.description.volume17
dc.description.issue5
dc.description.page553-564
dc.description.codenJOMIE
dc.identifier.isiutNOT_IN_WOS
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