光致聚合物
自愈水凝胶
光引发剂
聚合物
材料科学
生物相容性材料
甲基丙烯酸酯
曙红
化学工程
化学
生物医学工程
光强度
菁
高分子化学
聚合
纳米技术
明胶
曙红Y
组织工程
作者
Aya Gavish Moscovitz,Haneen Simaan Yameen,Orit Bar‐Am,Dror Seliktar
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-09-22
卷期号:26 (10): 6817-6833
被引量:11
标识
DOI:10.1021/acs.biomac.5c01142
摘要
Biomedical hydrogels often use a photopolymerization strategy to cross-link the polymer network. There are only a few cyto-compatible photoinitiators (PIs) that are commonly used for cross-linking biomedical hydrogels, including Irgacure 2959, lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP), and Eosin Y. Herein, we tested these PIs to optimize the cross-linking efficiency while minimizing cell death. Testing was performed on three types of hydrogels, including a synthetic material (poly(ethylene glycol)-diacrylate, PEG-DA), a semisynthetic material, PEG-fibrinogen (PF), and a modified biological material, methacrylated fibrinogen (FibMA). The results showed that PI concentration and illumination intensity had a significant impact on cross-linking efficiency, as measured by the shear storage modulus, with each material demonstrating different responses to the photopolymerization parameters. Optimal photo-cross-linking conditions were not the same for the modified protein hydrogels as compared to synthetic and semisynthetic materials. These findings may have consequential implications when applying photopolymerization to cross-link various types of cell-compatible hydrogels for biomedical applications.
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