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dc.contributor.authorÜstündaǧ Okur, Neslihan
dc.contributor.authorÖzdemir, Derya İlem
dc.contributor.authorGörgülü Kahyaoğlu, Şennur
dc.contributor.authorAy Şenyiğit, Zeynep
dc.contributor.authorAşıkoğlu, Makbule
dc.contributor.authorGenç, Lütfi
dc.contributor.authorKarasulu, Hatice Yeşim
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:51:40Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:51:40Z
dc.date.issued2016en_US
dc.identifier.citationÜstündaǧ Okur, N., Özdemir, D. İ., Görgülü Kahyaoğlu, Ş., Ay Şenyiğit, Z., Aşıkoğlu, M., Genç, L.ve Karasulu, H. Y. (2016). Assessment of aprotinin loaded microemulsion formulations for parenteral drug delivery: Preparation, characterization, in vitro release and cytotoxicity studies. Current Drug Delivery, 12(6), 668-679. https://dx.doi.org/10.2174/1567201812666150826091953en_US
dc.identifier.issn1567-2018
dc.identifier.issn1875-5704
dc.identifier.urihttps://dx.doi.org/10.2174/1567201812666150826091953
dc.identifier.urihttps://hdl.handle.net/20.500.12511/2263
dc.descriptionWOS: 000372334800004en_US
dc.descriptionPubMed ID: 26306401en_US
dc.description.abstractThe object of the current study was to prepare novel microemulsion formulations of aprotinin for parenteral delivery and to compare in vitro characteristics and release behaviour of different Technetium-99m (Tc-99m)-Aprotinin loaded microemulsion formulations. In addition, cytotoxicity of microemulsion formulation was evaluated with cell culture studies on human immortalized pancreatic duct epithelial-like cells. For this aim, firstly, pseudo-ternary phase diagrams were plotted to detect the formulation region and optimal microemulsions were characterized for their thermodynamic stability, conductivity, particle size, zeta potential, viscosity, pH and in vitro release properties. For in vitro release studies aprotinin was labelled with Tc-99m and labelling efficiency, radiochemical purity and stability of the radiolabeled complex were determined by several chromatography techniques. Radiolabeling efficiency of Tc-99m-Aprotinin was found over than 90% without any significant changes up to 6 hours after labelling at room temperature. After that, in vitro release studies of Tc-99m-Aprotinin loaded microemulsions were performed with two different methods; dissolution from diffusion cells and dialysis bags. Both methods showed that release rate of Tc-99m-Aprotinin from microemulsion could be controlled by microemulsion formulations. Drug release from the optimized microemulsion formulations was found lower compared to drug solution at the end of six hours. According to stability studies, the optimized formulation was found to be stable over a period of 12 months. Also, human immortalized pancreatic duct epithelial-like cells were used to evaluate the cytotoxicity of optimum formulation. Developed microemulsion did not reveal cytotoxicity. In conclusion the present study indicated that the M1-APT microemulsion is appropriate for intravenous application of aprotinin.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey [Tubitak-108S083]en_US
dc.description.sponsorshipThis study was supported by The Scientific and Technological Research Council of Turkey (Tubitak-108S083). We would like to acknowledge Ege University Pharmaceutical Sciences Research Center (FABAL) for enabling us to use its laboratory instruments. The authors would like to thank to Ege University, Faculty of Pharmacy, and Department of Microbiology. The authors would like to thank Ismail Ozturk for assistance at sterility experiments.en_US
dc.language.isoengen_US
dc.publisherBentham Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAprotininen_US
dc.subjectCytotoxicityen_US
dc.subjectIn Vitro Releaseen_US
dc.subjectMicroemulsionen_US
dc.subjectPancreatitisen_US
dc.subjectTc-99m-Aprotininen_US
dc.titleAssessment of aprotinin loaded microemulsion formulations for parenteral drug delivery: Preparation, characterization, in vitro release and cytotoxicity studiesen_US
dc.typearticleen_US
dc.relation.journalCurrent Drug Deliveryen_US
dc.departmentİstanbul Medipol Üniversitesi, Eczacılık Fakültesi, Eczacılık Teknolojisi Bölümü, Farmasötik Teknoloji Ana Bilim Dalıen_US
dc.authorid0000-0002-3210-3747en_US
dc.identifier.volume12en_US
dc.identifier.issue6en_US
dc.identifier.startpage668en_US
dc.identifier.endpage679en_US
dc.relation.ecinfo:eu-repo/grantAgreement/TUBITAK/SOBAG/Tubitak-108S083en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.2174/1567201812666150826091953en_US


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