Self‐Assembling Hydrogel for Controlled Release of <scp>bFGF</scp> and Ang‐1 Mimetic Peptide Promotes Neurovascular Repair in Ischemic Stroke Rats
Self-assembling peptide hydrogels represent a promising strategy for growth factor delivery and tissue repair, with the advantage of sustained release and micro-environment response characteristics. In the present study, a multiple biofunctional self-assembling hydrogels-FGFP/TIMP-AMP was constructed, which comprised three key components: (1) a basic fibroblast growth factor-mimetic peptide (FGFP), (2) an angiopoietin-1-mimetic peptide (AMP), and (3) a microenvironment-responsive TIMP sequence designed to target MMP-2. The FGFP/TIMP-AMP could assemble into a hydrogel under physiological conditions with a suitable pore size for cell growth. In vitro, it significantly promoted HUVEC migration and tube formation. Using a PC12 deprivation of oxygen and glucose (OGD) model, it effectively reduced apoptosis and protected against hypoxia. Furthermore, the bFGF/TIMP-AMP assembling hydrogels enhanced neuronal survival, vascular regeneration, and blood-brain barrier (BBB) repair in a middle cerebral artery occlusion (MCAO) rat model. These morphological improvements further promoted the recovery of motor function in behavioral tests. Therefore, these results highlighted the therapeutic potential of FGFP/TIMP-AMP assembling hydrogel for the repair of ischemic stroke.
Authors
- Ruyi Zhang (ORCID: https://orcid.org/0000-0002-3378-4601)
- Ran Li (ORCID: https://orcid.org/0000-0003-1526-0182)
- Haicheng Yuan
- Weihong Nie
- Ange Nie
- Na Zhou
- Chunying Shi
Institutions
- Qingdao University (CN)
- Weifang Medical University (CN)
- Affiliated Hospital of Qingdao University (CN)
- Qingdao Municipal Hospital (CN)
- Marine Biology Institute of Shandong Province (CN)
Publication Details
- Journal
- Journal of Biomedical Materials Research Part A
- Published
- 2026-03-23
- DOI
- https://doi.org/10.1002/jbm.a.70063
- Primary Topic
- Supramolecular Self-Assembly in Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00