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dc.contributor.authorGulsu, Aydan
dc.contributor.authorAyhan, Hakan
dc.contributor.authorAyhan, Fatma
dc.date.accessioned2020-11-20T16:23:09Z
dc.date.available2020-11-20T16:23:09Z
dc.date.issued2012
dc.identifier.issn0250-4685
dc.identifier.issn1303-829X
dc.identifier.urihttps://doi.org/10.5505/tjb.2012.21931
dc.identifier.urihttps://hdl.handle.net/20.500.12809/4224
dc.descriptionWOS: 000307444200002en_US
dc.description.abstractAim: Albumin microspheres have found many applications in the diagnosis and treatment in recent years and more than 100 diagnostic agents and drugs have been incorporated into Albumin microspheres. The objective of this study was to investigate the effect of preparation parameters (Albumin concentration, stirring rate, crosslinker amount, crosslinking time) on the Albumin microsphere size and determine the release profile of ketoprofen loaded albumin microsphere. Method: Albumin microspheres were prepared by an emulsion polymerization method using glutaraldehyde (GA) as the crosslinking agent. The prepared microspheres were then studied for their particle size, size distribution, release characteristics. The microspheres were characterized using an Optical Microscope. Results: The microspheres had mean diameters between 2-25 mu m of which more than 25 percent were below 10 mu m. Drug release from the Albumin microspheres displayed a biphasic pattern characterized by an initial fast release, followed by a slower release. The total amount of drug released from microspheres in pH 7.4 phosphate buffer saline (PBS) at 37 degrees C after 180 min was obtained as 33%. Conclusion: In the present study the various parameters affecting the characteristics of the albumin microspheres were evaluated. According to these results optimal conditions were determined as: 0.1 mg.ml(-1) Albumin concentration, 1000 rpm stirring rate, 1% GA amonut and 30 min crosslinking time. The drug release from Albumin microspheres was mainly controlled by diffusion and showed a biphasic pattern with initial release (burst effect), followed by a slow and controlled release phase resulting from controlled diffusion of the entrapped drug. Additionally, local gastrointestinal side effects are thought to be reduced by sustained release of ketoprofen and this must also be investigated with in vivo experiments.en_US
dc.item-language.isoengen_US
dc.publisherWalter de Gruyter Gmbhen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMicrospheresen_US
dc.subjectAlbuminen_US
dc.subjectKetoprofenen_US
dc.subjectBiodegradableen_US
dc.titlePreparation and characterization of ketoprofen loaded albumin microspheresen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTemp[Gulsu, Aydan; Ayhan, Fatma] Mugla Univ, Dept Chem, Div Biochem, TR-48000 Mugla, Turkeyen_US
dc.identifier.doi10.5505/tjb.2012.21931
dc.identifier.volume37en_US
dc.identifier.issue2en_US
dc.identifier.startpage120en_US
dc.identifier.endpage128en_US
dc.relation.journalTurkish Journal of Biochemistry-Turk Biyokimya Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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