Injectable and Tissue Adhesive Chitosan/Hyaluronic Acid-Based Hydrogels for Stem Cell Delivery and Cartilage Regeneration.
Lin X., Liu R., Gao Z., Zhou Y., Beitzel J., Noguchi A.
Laboratory Study on Knee Osteoarthritis, Osteoarthritis, Cartilage Damage, published in ACS Appl Bio Mater (2025) — summary generated from the PubMed abstract.
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
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 Appl Bio Mater (2025)
- Country
- United States
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 40490902
- DOI
- 10.1021/acsabm.5c00576
Abstract (original English)
Current therapeutic approaches for knee osteoarthritis (KOA) focus on symptom relief rather than addressing articular cartilage degeneration. Stem cell therapy holds promise for enhancing KOA treatment by promoting tissue regeneration, yet challenges remain in achieving minimally invasive delivery with sustained cell retention and viability. This study introduces an in situ fabricated, biodegradable, injectable, self-healing, tissue-adhesive hydrogel (Ald-HA/Dopa-HBCS). Formed by coinjecting two polymer solutions, it features a uniform, porous 3D structure, ideal for low-trauma administration and supporting human adipose-derived stem cells (hADSCs). We engineered its mechanical properties, gelation time, and degradation rate by adjusting polymer concentrations and ratios, ensuring hADSC viability for at least 14 days postinjection. Catechol groups provide tissue adhesion, enhancing therapeutic potential by retaining hADSCs at defect sites. The hydrogel also preserves chondrogenic gene expression and protein production in hADSCs, indicating broader applications beyond cartilage repair, extending to diverse cell-based therapies.
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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