自愈水凝胶
硫醇
马来酰亚胺
细胞包封
动力学
生物结合
材料科学
三维细胞培养
化学
高分子化学
生物物理学
细胞
纳米技术
有机化学
生物化学
物理
量子力学
生物
作者
Julieta I. Paez,Aleeza Farrukh,Rocío Valbuena-Mendoza,Małgorzata K. Włodarczyk‐Biegun,Aránzazu del Campo
标识
DOI:10.1021/acsami.0c00709
摘要
Thiol-maleimide and thiol-vinylsulfone cross-linked hydrogels are widely used systems in 3D culture models, in spite of presenting uncomfortable reaction kinetics for cell encapsulation: too fast (seconds for thiol-maleimide) or too slow (minutes-hours for thiol-vinylsulfone). Here, we introduce the thiol-methylsulfone reaction as alternative cross-linking chemistry for cell encapsulation, particularized for PEG-hydrogels. The thiol-methylsulfone reaction occurs at high conversion and at intermediate reaction speed (seconds-minutes) under physiological pH range. These properties allow easy mixing of hydrogel precursors and cells to render homogeneous cell-laden gels at comfortable experimental time scales. The resulting hydrogels are cytocompatible and show comparable hydrolytic stability to thiol-vinylsulfone gels. They allow direct bioconjugation of thiol-derivatized ligands and tunable degradation kinetics by cross-linking with degradable peptide sequences. 3D cell culture of two cell types, fibroblasts and human umbilical vein endothelial cells (HUVECs), is demonstrated.
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