Chitosan-glucose derivative membrane obtained by Maillard reaction improves cartilage repair in a rabbit model

被引:0
作者
Chuang, Po-Yao [1 ,2 ]
Chang, Shun-Fu [3 ]
Lu, Ying-Chen [4 ]
Huang, Kuo-Chin [1 ,2 ]
机构
[1] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[2] Chiayi Chang Gung Mem Hosp, Dept Orthopaed Surg, 6 West Sec,Chia Pu Rd, Pu Tz City 61363, Chiayi County, Taiwan
[3] Chiayi Chang Gung Mem Hosp, Dept Med Res & Dev, Chiayi, Taiwan
[4] Natl Chiayi Univ, Dept Food Sci, Chiayi, Taiwan
来源
JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH | 2024年 / 19卷 / 01期
关键词
Chitosan; Maillard reaction; Osteochondral defect; Cartilage; Biomaterial; CHONDROCYTE; BONE;
D O I
10.1186/s13018-024-05127-7
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
BackgroundTreatment of articular cartilage injury remains a challenging clinical problem in orthopedics. Chitosan-derived biomaterial could be a potential adjuvant treatment to improve cartilage repair. In the current study, we examined the effects of two potential chitosan-derived materials on cartilage regeneration of osteochondral defects in rabbits. MethodsAn osteochondral defect was created over the rabbit knee and treated using three approaches: group A received no material (n = 24), group B received chitosan membranes with glucose absorption (CGA; n = 25), and group C received chitosan-glucose derivative membranes obtained via the Maillard reaction (CGMR; n = 25). Cartilage repair over the osteochondral defect was analyzed 12 weeks post-surgery via histological analysis, immunostaining, and reverse transcription-qualitative polymerase chain reaction (RT-qPCR) for type-I and type-II collagen mRNA. ResultsAccording to histological analysis, CGMR-treated defects showed significantly improved modified O'Driscoll scoring when compared with no material- and CGA-treated defects (20.9 +/- 4.3 vs. 13.00 +/- 2.5 and 17.7 +/- 4.6, p < 0.001). Moreover, group C exhibited higher intensity of type-II collagen immunohistochemical staining over the regenerated cartilage than groups A and B, along with increased expression of type-II collagen mRNA by RT-qPCR. ConclusionsCGMR might improve cartilage regeneration in osteochondral defects.
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页数:9
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