Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/106049
DC FieldValue
dc.titleInfluence of hydroxypropylmethyl cellulose and sodium carboxymethyl cellulose as coating polymers on drug release from spheroids
dc.contributor.authorWan, L.S.C.
dc.contributor.authorHeng, P.W.S.
dc.contributor.authorTan, Y.T.F.
dc.date.accessioned2014-10-29T01:54:18Z
dc.date.available2014-10-29T01:54:18Z
dc.date.issued1995
dc.identifier.citationWan, L.S.C.,Heng, P.W.S.,Tan, Y.T.F. (1995). Influence of hydroxypropylmethyl cellulose and sodium carboxymethyl cellulose as coating polymers on drug release from spheroids. S.T.P. Pharma Sciences 5 (2) : 128-133. ScholarBank@NUS Repository.
dc.identifier.issn11571489
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106049
dc.description.abstractThe formulation of cellulose ether coated controlled-release spheroids containing chlorpheniramine maleate was described. The drug cores were prepared using a rotoprocessor and then coated with hydrophilic polymers using a bottom-spray fluidized-bed coater. Polymeric dispersion of either hydroxypropylmethyl cellulose (HPMC) or sodium carboxymethyl cellulose (NaCMC), as well as a mixture of both, were used as the coating solutions. Drug release from spheroids coated with single polymer of HPMC or NaCMC was reduced with an increase in coating levels. Drug release from spheroids coated with a mixture of HPMC and NaCMC (1/1) showed longer dissolution T(50%) values as compared with spheroids coated with a single polymer at the corresponding coating levels. When spheroids were coated with two polymers, HPMC and NaCMC, one following the other, the relative position of the polymer governs the drug release profile. All the release kinetics exhibited a biexponential first-order model.
dc.sourceScopus
dc.subjectdissolution profile
dc.subjecthydroxypropylmethyl cellulose
dc.subjectpolymer coating
dc.subjectrelease kinetics
dc.subjectsodium carboxymethyl cellulose
dc.subjectspheroids
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.sourcetitleS.T.P. Pharma Sciences
dc.description.volume5
dc.description.issue2
dc.description.page128-133
dc.description.codenSTSSE
dc.identifier.isiutNOT_IN_WOS
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