Level D· Scientific groundwork from lab and animal studiesLaboratory StudyPubMedOpen access

Injectable Thermosensitive Thiol-Modified NIPAAm- g -Chitosan Hydrogels for Cartilage Regeneration in a Rabbit Osteoarthritis Model.

Ching PCO., Chang YC., Weng CH., Wang JS., Yeh ML.

Laboratory Study on Osteoarthritis, Cartilage Damage, published in ACS Omega (2025) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
ACS Omega (2025)
Country
United States
Reported sample size
—
Source database
PubMed
PMID
40060830
PMCID
PMC11886913
DOI
10.1021/acsomega.4c10829
Citations
2

Abstract (original English)

Cartilage tissue has a limited intrinsic capacity for self-healing. Over the decades, researchers have extensively researched methods of cartilage repair, yet some limitations still need to be resolved. Most studies typically evaluate osteochondral regeneration in normal animals. However, traumatic articular cartilage defects may eventually result in osteoarthritis (OA), and the relationship between cartilage defects and OA is not independent. Therefore, in this study, the effect of thiol-modified NIPAAm- g -chitosan (TNC) hydrogels containing human adipose-derived mesenchymal stem cells (hADMSCs), with or without etanercept, a TNF-α inhibitor, was evaluated for cartilage regeneration in a monosodium iodoacetate (MIA)-induced OA rabbit model. TNC hydrogels, with a suitable lower critical solution temperature (LCST), porous interior microstructures, enhanced mechanical properties, and without cytotoxicity were synthesized and characterized by DSC, SEM, NMR, and the CCK8 kit. The OA rabbit models were established by MIA injection in the rabbit knees and verified with histological examinations and cytokine detection for IL-1β, IL-6, and TNF-α. According to macroscopic evaluations, micro-CT analysis, and histological and immunohistochemical evaluations, the results of cartilage repair in OA models showed improvement in cartilage regeneration in the cell-seeded hydrogel groups compa

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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