Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1893
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dc.contributor.authorYammine, Paoloen_US
dc.contributor.authorMaarawi, Thereseen_US
dc.contributor.authorMoussa, Dimaen_US
dc.contributor.authorAbdel-Massih, Roulaen_US
dc.contributor.authorKassab, Rimaen_US
dc.date.accessioned2020-12-23T09:02:19Z-
dc.date.available2020-12-23T09:02:19Z-
dc.date.issued2015-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1893-
dc.description.abstractMicroencapsulation by the solvent evaporation technique was used to formulate Indomethacin-loaded poly(DL-lactide-co-caprolactone) microspheres with three different surfactants: Tween 80, Span 80, and Polyvinyl alcohol. Different formulations were prepared by changing drug masses, while keeping the quantities of the polymer and of the surfactant constant. The prepared microspheres were evaluated for drug content, particle size, morphology, drug-polymer interaction, stability, in vitro release, and cytotoxicity assays. Comparison was done to study the effects of the surfactant type on their characteristics. Microspheres presented a spherical and porous profile and were characterized by the stable character of the encapsulated drug. The usage of the Polyvinyl alcohol revealed the highest percent drug entrapment and drug loading, the biggest particles sizes, and the lowest drug release rate. It was the opposite in the case of Tween 80. A negligible cytotoxic effect was noted on Polyvinyl alcohol formulations having the highest drug content. Polymeric microspheres were used efficiently as a delivery system for Indomethacin. Changing the surfactant type had many advantages on drug encapsulation and release rate.en_US
dc.format.extent10 p.en_US
dc.language.isoengen_US
dc.subjectDrug deliveryen_US
dc.subjectDrugsen_US
dc.subjectMicroencapsulationen_US
dc.subjectIn vitro releaseen_US
dc.subject.lcshPolymersen_US
dc.titleEffect of different surfactants on indomethacin microspheres formulationen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Medical Laboratory Sciencesen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume11en_US
dc.description.issue4en_US
dc.description.startpage3454en_US
dc.description.endpage3464en_US
dc.date.catalogued2017-10-27-
dc.description.statusPublisheden_US
dc.identifier.OlibID174589-
dc.identifier.openURLhttps://cirworld.com/index.php/jac/article/view/2204en_US
dc.relation.ispartoftextJournal of advances in chemistryen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Biology
Department of Chemistry
Department of Medical Laboratory Sciences
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