Evidence map›Paper›PMID 39367411›Full record

ArticleJournal of orthopaedic surgery and research2024

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

Po-Yao Chuang, Shun-Fu Chang, Ying-Chen Lu, Kuo-Chin Huang

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Po-Yao ChuangCollege of Medicine, Chang Gung University, Taoyuan, Taiwan.
Shun-Fu ChangDepartment of Medical Research and Development, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan.
Ying-Chen LuDepartment of Food Science, National Chiayi University, Chiayi, Taiwan.
Kuo-Chin HuangCollege of Medicine, Chang Gung University, Taoyuan, Taiwan. kc2672@gmail.com.

Funding

Chiayi Chang Gung Memorial Hospital, Taiwan CMRPG6H0611-2 and CMRPG6K0051
6 · The paper itself

Abstract

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.

Indexed as

Cartilage, ArticularChitosanGlucoseMaillard ReactionAnimalsBiocompatible MaterialsDisease Models, AnimalMaleMembranes, ArtificialRabbitsRegenerationBiocompatible MaterialsChitosanGlucoseMembranes, ArtificialBiomaterialCartilageChitosanMaillard reactionOsteochondral defect

Identifiers

PMID39367411
PMCPMC11453087

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.