Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/8637
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dc.contributor.authorCetik, Riza Mert-
dc.contributor.authorCiftci, Samiye Yabanoglu-
dc.contributor.authorArica, Betul-
dc.contributor.authorBaysal, Ipek-
dc.contributor.authorDizakar, Saadet Ozen Akarca-
dc.contributor.authorErbay Elibol, Fatma Kübra-
dc.contributor.authorDemir, Teyfik-
dc.date.accessioned2022-07-30T16:43:40Z-
dc.date.available2022-07-30T16:43:40Z-
dc.date.issued2022-
dc.identifier.citationCetik, R. M., Yabanoglu Ciftci, S., Arica, B., Baysal, I., Akarca Dizakar, S. O., Erbay Elibol, F. K., ... & Ayvaz, M. (2022). Evaluation of the Effects of Transforming Growth Factor–Beta 3 (TGF-?3) Loaded Nanoparticles on Healing in a Rat Achilles Tendon Injury Model. The American Journal of Sports Medicine, 50(4), 1066-1077.en_US
dc.identifier.issn0363-5465-
dc.identifier.issn1552-3365-
dc.identifier.urihttps://doi.org/10.1177/03635465211073148-
dc.identifier.urihttps://hdl.handle.net/20.500.11851/8637-
dc.description.abstractBackground: Achilles tendon (AT) midsubstance injuries may heal suboptimally, especially in athletes. Transforming growth factor-beta 3 (TGF-beta 3) shows promise because of its recently discovered tendinogenic effects. Using poly(lactic-co-glycolic acid)-b-poly(ethylene glycol) (PLGA-b-PEG) nanoparticles (NPs) may enhance the results by a sustained-release effect. Hypothesis: The application of TGF-beta 3 will enhance AT midsubstance healing, and the NP form will achieve better outcomes. Study Design: Controlled laboratory study. Methods: A total of 80 rats underwent unilateral AT transection and were divided into 4 groups: (1) control (C); (2) empty chitosan film (Ch); (3) chitosan film containing free TGF-beta 3 (ChT); and (4) chitosan film containing TGF-beta 3-loaded NPs (ChN). The animals were sacrificed at 3 and 6 weeks. Tendons were evaluated for morphology (length and cross-sectional area [CSA]), biomechanics (maximum load, stress, stiffness, and elastic modulus), histology, immunohistochemical quantification (types I and III collagen [COL1 and COL3]), and gene expression (COL1A1, COL3A1, scleraxis, and tenomodulin). Results: Morphologically, at 3 weeks, ChT (15 +/- 2.7 mm) and ChN (15.6 +/- 1.6 mm) were shorter than C (17.6 +/- 1.8 mm) (P = .019 and = .004, respectively). At 6 weeks, the mean CSA of ChN (10.4 +/- 1.9 mm(2)) was similar to that of intact tendons (6.4 +/- 1.1 mm(2)) (P = .230), while the other groups were larger. Biomechanically, at 3 weeks, ChT (42.8 +/- 4.9 N) had a higher maximum load than C (27 +/- 9.1 N; P = .004) and Ch (29.2 +/- 5.7 N; P = .005). At 6 weeks, ChN (26.9 +/- 3.9 MPa) had similar maximum stress when compared with intact tendons (34.1 +/- 7.8 MPa) (P = .121); the other groups were significantly lower. Histologically, at 6 weeks, the mean Movin score of ChN (4.5 +/- 1.5) was lower than that of ChT (6.3 +/- 1.8). Immunohistochemically, ChN had higher COL3 (1.469 +/- 0.514) at 3 weeks and lower COL1 (1.129 +/- 0.368) at 6 weeks. COL1A1 gene expression was higher in ChT and ChN at 3 weeks, but COL3A1 gene expression was higher in ChN. Conclusion: The application of TGF-beta 3 had a positive effect on AT midsubstance healing, and the sustained-release NP form improved the outcomes, more specifically accelerating the remodeling process.en_US
dc.language.isoenen_US
dc.publisherSage Publications Incen_US
dc.relation.ispartofAmerican Journal of Sports Medicineen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAchilles tendonen_US
dc.subjectTGF-beta 3en_US
dc.subjectPLGA-b-PEGen_US
dc.subjectnanoparticleen_US
dc.subjectTgf-Betaen_US
dc.subjectGene-Expressionen_US
dc.subjectStem-Cellsen_US
dc.subjectRepairen_US
dc.subjectChitosanen_US
dc.subjectRuptureen_US
dc.subjectMatrixen_US
dc.subjectDifferentiationen_US
dc.subjectReturnen_US
dc.subjectTissueen_US
dc.titleEvaluation of the Effects of Transforming Growth Factor-Beta 3 (tgf-Beta 3) Loaded Nanoparticles on Healing in a Rat Achilles Tendon Injury Modelen_US
dc.typeArticleen_US
dc.departmentFakülteler, Mühendislik Fakültesi, Biyomedikal Mühendisliği Bölümüen_US
dc.departmentFakülteler, Mühendislik Fakültesi, Makine Mühendisliği Bölümüen_US
dc.departmentFaculties, Faculty of Engineering, Department of Biomedical Engineeringen_US
dc.departmentFaculties, Faculty of Engineering, Department of Mechanical Engineeringen_US
dc.identifier.volume50en_US
dc.identifier.issue4en_US
dc.identifier.startpage1066en_US
dc.identifier.endpage1077en_US
dc.authoridBaysal, Ipek/0000-0002-9607-4199-
dc.authoridDİZAKAR, Saadet Özen AKARCA/0000-0002-4358-6510-
dc.identifier.wosWOS:000759942900001en_US
dc.identifier.scopus2-s2.0-85125047173en_US
dc.institutionauthorErbay Elibol, Fatma Kübra-
dc.institutionauthorDemir, Teyfik-
dc.identifier.pmid35188807en_US
dc.identifier.doi10.1177/03635465211073148-
dc.authorwosidBaysal, Ipek/I-8429-2013-
dc.authorwosidDİZAKAR, Saadet Özen AKARCA/AAA-1367-2021-
dc.authorscopusid57207940153-
dc.authorscopusid57203217262-
dc.authorscopusid6507938268-
dc.authorscopusid55317225300-
dc.authorscopusid57201548039-
dc.authorscopusid57205645750-
dc.authorscopusid57222071875-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ1-
item.openairetypeArticle-
item.languageiso639-1en-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.dept02.2. Department of Biomedical Engineering-
Appears in Collections:Bilgisayar Mühendisliği Bölümü / Department of Computer Engineering
Makine Mühendisliği Bölümü / Department of Mechanical Engineering
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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