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Effects of adipose tissue-derived stromal vascular fraction on osteochondral defects treated by hyaluronic acid-based scaffold: An experimental study

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dc.contributor.author Sahin, Abdullah Alper
dc.contributor.author Degirmenci, Erdem
dc.contributor.author Ozturan, Kutay Engin
dc.contributor.author Firat, Tulin
dc.contributor.author Kukner, Aysel
dc.date.accessioned 2023-01-06T12:06:08Z
dc.date.available 2023-01-06T12:06:08Z
dc.date.issued 2021
dc.identifier.citation Sahin, AA., Degirmenci, E., Ozturan, KE., Firat, T., Kukner, A. (2021). Effects of adipose tissue-derived stromal vascular fraction on osteochondral defects treated by hyaluronic acid-based scaffold: An experimental study. Joint Diseases and Related Surgery, 32(2), 347-354.Doi:10.52312/jdrs.2021.19 en_US
dc.identifier.isbn 2687-4784
dc.identifier.isbn 2687-4792
dc.identifier.uri http://dx.doi.org/10.52312/jdrs.2021.19
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:000661415100010
dc.identifier.uri https://pubmed.ncbi.nlm.nih.gov/34145810
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3619
dc.description WoS Categories : Orthopedics; Surgery Web of Science Index : Science Citation Index Expanded (SCI-EXPANDED) Research Areas : Orthopedics; Surgery Open Access Designations : Green Published, gold en_US
dc.description.abstract Objectives: This study aims to evaluate the effect of adipose-derived stromal vascular fraction (SVF) on osteochondral defects treated by hyaluronic acid (HA)-based scaffold in a rabbit model. Materials and methods: Eighteen white New Zealand rabbits were randomly grouped into the experimental group (n=9) and control group (n=9). In all groups, osteochondral defects were induced on the weight-bearing surfaces of the right femoral medial condyles, and a HA-based scaffold was applied to the defect area with microfractures (MFs). In this study, 1 mL of adipose-derived SVF was injected into the knee joints of the rabbits in the experimental group. For histological and macroscopic evaluation, four rabbits were randomly selected from each group at Week 4, and the remaining rabbits were sacrificed at the end of Week 8. Macroscopic assessments of all samples were performed based on the Brittberg scoring system, and microscopic evaluations were performed based on the O'Driscoll scores. Results: Samples were taken at Weeks 4 and 8. At Week 4, the O'Driscoll scores were significantly higher in the control group than the experimental group (p=0.038), while there was no significant difference in the Brittberg scores between the two groups (p=0.108). At Week 8, the O'Driscoll score and Brittberg scores were statistically higher in the experimental group than in the control group (p=0.008 and p=0.007, respectively). According to the microscopic evaluation, at the end of Week 8, the cartilage thickness was greater in the experimental group, and nearly all of the defect area was filled with hyaline cartilage. Conclusion: Application of adipose-derived SVF with MF-HA-based scaffold was better than MF-HA-based scaffold treatment in improving osteochondral regeneration. Therefore, it can be used in combination with microfracture and scaffold to accelerate cartilage regeneration, particularly in the treatment of secondary osteoarthritis. en_US
dc.language.iso eng en_US
dc.publisher TURKISH JOINT DISEASES FOUNDATION CANKARA en_US
dc.relation.isversionof 10.52312/jdrs.2021.19 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject MESENCHYMAL STEM-CELLS; ARTHROSCOPIC MICROFRACTURE; CARTILAGE; REPAIR; RAT; INJECTION en_US
dc.subject Acellular matrix scaffold; adipose tissue; osteochondral defect; stem cell; stromal vascular fraction en_US
dc.title Effects of adipose tissue-derived stromal vascular fraction on osteochondral defects treated by hyaluronic acid-based scaffold: An experimental study en_US
dc.type article en_US
dc.relation.journal JOINT DISEASES AND RELATED SURGERY en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.identifier.volume 32 en_US
dc.identifier.issue 2 en_US
dc.identifier.startpage 347 en_US
dc.identifier.endpage 354 en_US


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