Double-crosslinked carrageenan/gelatin hydrogel loaded with heparin for heart valve tissue engineering applications.
Guo C., Ye W., Huang J., Xiao J., Lu D., Gao B.
Animal Study on Systemic / IV, published in Biomed Mater (2026) — 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
- Animal Study
- Journal
- Biomed Mater (2026)
- Country
- England
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 41871531
- DOI
- 10.1088/1748-605X/ae55ee
Abstract (original English)
The development of tissue-engineered heart valves (TEHVs) remains a challenge worldwide. In this study, a series of double-crosslinked methacrylated (MA) carrageenan (CA)/MA gelatin hydrogels loaded with heparin (CA/Gel@Hep) were developed as potential materials for TEHV. CA/Gel@Hep hydrogels with different concentrations of heparin were fabricated, and their mechanical properties, swelling/degradation behaviors, and heparin release profiles, and biological performance were systematically studied. The rheological tests showed that storage modulus ( G ') was consistently higher than loss modulus ( G ''). Unconfined compression tests showed that the compressive modulus of CA/Gel@Hep hydrogels ranged from 0.26 ± 0.01 to 0.43 ± 0.03 kPa, which matches the mechanical requirements of native valve leaflets. In vitro evaluation demonstrated that CA/Gel@Hep hydrogels exhibited good cytocompatibility and blood compatibility, excellent anticoagulant properties, and facilitated migration and proliferation of human adipose tissue-derived mesenchymal stromal cells. quantitative PCR results showed that CA/Gel@Hep hydrogels significantly upregulated the expression of genes related to valve remodeling, including SMA, VIM, MMP1, and MMP2. These results suggest that CA/Gel@Hep hydrogels hold great potential for heart valve tissue engineering applications.
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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