Publication:
Effect of drug properties on physical and release characteristics of Eudragit microspheres prepared by spherical crystallization technique

dc.contributor.authorsAkbuga, J; Bergisadi, N
dc.date.accessioned2022-03-12T16:56:27Z
dc.date.accessioned2026-01-11T15:22:29Z
dc.date.available2022-03-12T16:56:27Z
dc.date.issued1997
dc.description.abstractTen compounds having different solubilities and molecular weights were evaluated for incorporation into Eudragit microspheres using the spherical crystallization technique, and the effects of drug-related factors on the properties of Eudragit microspheres were investigated. The entrapment of the active compound within the microspheres was highly dependent on the acidic or basic characteristics of the drug. Structural changes were also observed on the microsphere surface prepared at different pH values. Microspheres prepared with slightly and very slightly soluble drugs such as salicylic acid, naproxen, piroxicam, indomethacin, and methylprednisolone indicated controlled-release properties. Generally, drug release from microspheres followed the Fickian diffusion model.
dc.identifier.doi10.3109/03639049709146145
dc.identifier.issn0363-9045
dc.identifier.urihttps://hdl.handle.net/11424/226761
dc.identifier.wosWOS:A1997WM97200012
dc.language.isoeng
dc.publisherMARCEL DEKKER INC
dc.relation.ispartofDRUG DEVELOPMENT AND INDUSTRIAL PHARMACY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSOLVENT EVAPORATION METHOD
dc.subjectACID
dc.titleEffect of drug properties on physical and release characteristics of Eudragit microspheres prepared by spherical crystallization technique
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage411
oaire.citation.issue4
oaire.citation.startPage407
oaire.citation.titleDRUG DEVELOPMENT AND INDUSTRIAL PHARMACY
oaire.citation.volume23

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