Decellularization of Trachea With Combined Techniques for Tissue-Engineered Trachea Transplantation

dc.contributor.authorBatioglu-Karaaltin, Aysegul
dc.contributor.authorOvali, Ercument
dc.contributor.authorKaraaltin V, Mehmet
dc.contributor.authorYener, Murat
dc.contributor.authorYilmaz, Mehmet
dc.contributor.authorEpupoglu, Fatma
dc.contributor.authorYilmaz, Yetkin Zeki
dc.contributor.authorBozkurt, Erol Rustu
dc.contributor.authorDemir, Necdet
dc.contributor.authorKonuk, Esma
dc.contributor.authorBozdag, Ergun Sureyya
dc.contributor.authorYigit, Ozgur
dc.contributor.authorCansiz, Harun
dc.date.accessioned2023-02-21T12:39:46Z
dc.date.available2023-02-21T12:39:46Z
dc.date.issued2019-01-01
dc.description.abstractObjectives. The purpose of this study is to shorten the decellularization time of trachea by using combination of physical, chemical, and enzymatic techniques. Methods. Approximately 3.5-cm-long tracheal segments from 42 New Zealand rabbits (3.5 +/- 0.5 kg) were separated into seven groups according to decellularization protocols. After decellularization, cellular regions, matrix and strength and endurance of the scaffold were followed up. Results. DNA content in all groups was measured under 50 ng/mg and there was no significant difference for the glycosaminoglycan content between group 3 (lyophilization+deoxycholic acid+de-oxyribonuclease method) and control group (P=0.46). None of the decellularized groups was different than the normal trachea in tensile stress values (P>0.05). Glucose consumption and lactic acid levels measured from supernatants of all decellularized groups were close to group with cells only (76 mg/dl, and 53 mg/L). Conclusion. Using combination methods may reduce exposure to chemicals, prevent the excessive influence of the matrix, and shorten the decellularization time.
dc.description.issue1
dc.description.issueFEB
dc.description.pages86-94
dc.description.volume12
dc.identifier.doi10.21053/ceo.2018.00486
dc.identifier.urihttps://hdl.handle.net/11443/2542
dc.identifier.urihttp://dx.doi.org/10.21053/ceo.2018.00486
dc.identifier.wosWOS:000454984200012
dc.publisherKOREAN SOC OTORHINOLARYNGOL
dc.relation.ispartofCLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY
dc.subjectTrachea
dc.subjectScaffold
dc.subjectFreeze Drying
dc.subjectTissue Engineering
dc.subjectDeoxycholic Acid
dc.titleDecellularization of Trachea With Combined Techniques for Tissue-Engineered Trachea Transplantation
dc.typeArticle

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