Li Zhili, Zhou Dezhong
School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, China.
Biomacromolecules. 2024 Sep 9;25(9):6195-6202. doi: 10.1021/acs.biomac.4c01051. Epub 2024 Aug 13.
Poly(ethylene glycol) (PEG)-based hydrogels are particularly challenging to degrade, which hinders efficient cell harvesting within the gel matrix. Here, highly branched copolymers of PEG methyl ether acrylate (PEGMA) and disulfide diacrylate (DSDA) (PEG-DS) with short primary chains and multiple pendent vinyl groups were synthesized by a "vinyl oligomer combination" approach. PEG-DS readily cross-links with thiolated gelatin (Gel-SH) to form hydrogels. Results demonstrate that shortening the primary chains of PEG-DS significantly enhances the viability of bone marrow mesenchymal stem cells (BMSCs) by up to 193.2%. Importantly, DS junctions can be easily cleaved into short primary chains using dithiothreitol (DTT), triggering ultrafast degradation of PEG-DS/Gel-SH hydrogels within 2 min under mild conditions and release of the encapsulated BMSCs. This study establishes a novel strategy to enhance the degradation of acrylate-based PEG hydrogels for three-dimensional (3D) cell culture and harvesting. These findings expand the potential applications of such hydrogels in various biomedical fields.
基于聚乙二醇(PEG)的水凝胶特别难以降解,这阻碍了在凝胶基质内高效收获细胞。在此,通过“乙烯基低聚物组合”方法合成了具有短主链和多个侧链乙烯基的聚乙二醇甲基醚丙烯酸酯(PEGMA)和二硫代二丙烯酸酯(DSDA)的高度支化共聚物(PEG-DS)。PEG-DS很容易与硫醇化明胶(Gel-SH)交联形成水凝胶。结果表明,缩短PEG-DS的主链可显著提高骨髓间充质干细胞(BMSC)的活力,最高可达193.2%。重要的是,使用二硫苏糖醇(DTT)可轻松将DS连接点切割成短主链,在温和条件下2分钟内引发PEG-DS/Gel-SH水凝胶的超快降解,并释放包封的BMSC。本研究建立了一种新策略,以增强用于三维(3D)细胞培养和收获的丙烯酸酯基PEG水凝胶的降解。这些发现扩展了此类水凝胶在各种生物医学领域的潜在应用。