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dc.contributor.authorDemirbilek, Murat
dc.contributor.authorTürkoğlu Laçin, Melisa
dc.contributor.authorAktürk, Selçuk
dc.date.accessioned2020-01-29T09:25:25Z
dc.date.available2020-01-29T09:25:25Z
dc.date.issued2017
dc.identifier.issn1300-0152
dc.identifier.urihttps://doi.org/10.3906/biy-1704-31
dc.identifier.urihttp://hdl.handle.net/11655/21906
dc.description.abstractIn the treatment of dermal wounds, wound-dressing materials prepared from natural mucopolysaccharides are widely used because of their advantages such as nonirritation, nontoxicity, and ease in topical application. In the present study, alginate hydrogels modified with N-acetyl glucose amine (NAG) were prepared as wound-dressing material. Physical, chemical, thermal, and mechanical properties of the hydrogels were studied. Cytotoxicity of the hydrogels on endothelial (HUVEC) and keratinocyte (HaCaT) cells were examined. Anti-and proinflammatory cytokine levels of human monocyte-macrophage cells (THP-1) stimulated with hydrogels were determined. According to the results, increasing the NAG concentration led to an increase in the swelling and nitrogen ratios in the hydrogels. Additionally, increasing the NAG concentration decreased elastic modulus and degradation time. Hydrogels were not cytotoxic on HaCaT and HUVEC cells. It stimulated IL-10 and TNF-alpha levels at a small rate.tr_TR
dc.language.isoentr_TR
dc.publisherTubitak Scientific & Technical Research Council Turkeytr_TR
dc.relation.isversionof10.3906/biy-1704-31tr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.subjectBiomaterialstr_TR
dc.subjectAlginate hydrogelstr_TR
dc.subjectHyaluronic acid monomerstr_TR
dc.subjectCytokinestr_TR
dc.subject.lcshMikroteknolojitr_TR
dc.titleN-Acetylglucoseamine Modified Alginate Sponges As Scaffolds For Skin Tissue Engineeringtr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.relation.journalTurkish Journal Of Biologytr_TR
dc.contributor.departmentNanoteknoloji ve Nanotıptr_TR
dc.identifier.volume41tr_TR
dc.identifier.issue5tr_TR
dc.identifier.startpage796tr_TR
dc.identifier.endpage807tr_TR
dc.description.indexWoStr_TR
dc.description.indexScopustr_TR
dc.fundingYoktr_TR


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