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dc.contributor.authorGuncum, Enes
dc.contributor.authorIsiklan, Nuran
dc.contributor.authorAnlas, Ceren
dc.contributor.authorUnal, Nilgun
dc.contributor.authorBulut, Elif
dc.contributor.authorBakirel, Tulay
dc.date.accessioned2020-06-25T18:29:47Z
dc.date.available2020-06-25T18:29:47Z
dc.date.issued2018
dc.identifier.citationEnes Güncüm, Nuran Işıklan, Ceren Anlaş, Nilgün Ünal, Elif Bulut & Tülay Bakırel (2018) Development and characterization of polymeric-based nanoparticles for sustained release of amoxicillin – an antimicrobial drug, Artificial Cells, Nanomedicine, and Biotechnology, 46:sup2, 964-973.en_US
dc.identifier.issn2169-1401
dc.identifier.issn2169-141X
dc.identifier.urihttps://doi.org/10.1080/21691401.2018.1476371
dc.identifier.urihttps://hdl.handle.net/20.500.12587/7463
dc.descriptionBakirel, Tulay/0000-0001-5805-2178en_US
dc.descriptionWOS: 000459181400092en_US
dc.descriptionPubMed: 29806495en_US
dc.description.abstractIn this study, amoxicillin (AMO)-loaded poly(vinyl alcohol)/sodium alginate (PVA/NaAlg) nanoparticles were prepared as a polymer-based controlled release system. The physicochemical properties of the obtained nanoparticles were investigated by XRD, DSC/TGA, particle size analyses and zeta potential measurements. The average particle sizes were in the range from 336.3 +/- 25.66 to 558.3 +/- 31.39 nm with negative zeta potential values from -41.86 +/- 0.55 to-47.3 +/- 2.76 mV. The influences of PVA/NaAlg ratio, span 80 concentration, exposure time to glutaraldehyde (GA) and the drug/polymer ratio on AMO release profiles were evaluated. In vitro drug release studies showed a controlled and pH dependent AMO release with an initial burst effect. XRD patterns and DSC thermograms of AMO-loaded nanoparticles revealed that the drug in the nanoparticles was in amorphous form, which was more stable than the crystalline form. The antibacterial activity of the optimal formulation was also investigated. The minimum inhibitory concentration (MIC) values of this formulation had the comparable antibacterial activity with that of pure AMO. These results indicate that the developed nanoparticles could be a promising candidate drug delivery system for AMO.en_US
dc.description.sponsorshipDepartment of Scientific Research Projects, Istanbul UniversityIstanbul University [44188]en_US
dc.description.sponsorshipThis work was supported by Department of Scientific Research Projects, Istanbul University [Project number: 44188].en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.isversionof10.1080/21691401.2018.1476371en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAmoxicillinen_US
dc.subjectpolymeric nanocarrieren_US
dc.subjectsustained releaseen_US
dc.subjectoral drug deliveryen_US
dc.titleDevelopment and characterization of polymeric-based nanoparticles for sustained release of amoxicillin - an antimicrobial drugen_US
dc.typearticleen_US
dc.contributor.departmentKırıkkale Üniversitesien_US
dc.identifier.volume46en_US
dc.identifier.startpage964en_US
dc.identifier.endpage973en_US
dc.relation.journalArtificial Cells Nanomedicine And Biotechnologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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