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A Dual-Dynamically Crosslinked Hydrogel for Cardiac Repair with Microenvironment Regulation and Angiogenic Functions

Authors: ZHANG Haitao; LIANG Lei; YUE Zhiwei; WANG Chengyao; CHEN Linyu; LU Jiajun; ZHANG Hong; YAO Fanglian; SUN Hong; LI Junjie

DOI: 10.1007/s40843-025-3619-1Status: Verified Translated Edition
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Key Findings in This Report

• • SA-PBA/E/Sr hydrogel reduced infarct size and increased left ventricular wall thickness, with Masson's staining showing significantly less collagen deposition (blue) compared to MI groups (***P < 0.001), indicating effective mitigation of fibrosis and scar tissue formation. • • The hydrogel promoted macrophage polarization from pro-inflammatory M1 to anti-inflammatory M2 phenotype, decreasing TNF-α secretion and increasing IL-10 production, which is critical for resolving inflammation and fostering a pro-repair microenvironment. • • Incorporation of Sr2+ significantly enhanced endothelial cell migration, a key factor in angiogenesis, leading to accelerated neovascularization in the infarcted tissue, as evidenced by increased vessel density. • • Echocardiographic analysis demonstrated a remarkable increase in ejection fraction and reduced left ventricular dilation, confirming significant cardiac functional recovery after SA-PBA/E/Sr treatment compared to other groups.