Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Biomater Sci. 2017 Nov 21;5(12):2398-2402. doi: 10.1039/c7bm00669a.
A hindered urea bond (HUB), recently reported as a new type of dynamic chemical bond, can be facilely constructed by mixing an isocyanate and a hindered amine. Here, we report the use of the HUB in the design of degradable hydrogel materials for applications of stem cell encapsulation and delivery. Polyethyleneglycol (PEG) diamine was end-capped with a HUB and an allyl group in a one-pot synthesis. The resulting polymer was cross-linked to form a hydrogel under UV with the addition of a 4-arm PEG thiol and a photoinitiator. The degradation properties of the hydrogels were confirmed with NMR, GPC, weight loss, and protein release studies. We found that the degradation kinetics is dependent on the size of the N-substituents, and the one with the tert-butyl group shows complete degradation within 2 days. The new hydrogel materials were also demonstrated to be biocompatible with hMSCs, and the cell release kinetics can be facilely tuned over 5 days.
受阻脲键(HUB)是一种新型动态化学键,最近有报道称其可通过混合异氰酸酯和受阻胺轻松构建。在这里,我们报告了在设计用于干细胞包封和递送的可降解水凝胶材料中使用 HUB。在一锅合成中,将聚乙二醇二胺的末端用 HUB 和烯丙基封端。所得聚合物在添加四臂 PEG 硫醇和光引发剂的情况下,通过 UV 交联形成水凝胶。通过 NMR、GPC、失重和蛋白质释放研究证实了水凝胶的降解性能。我们发现,降解动力学取决于 N-取代基的大小,而叔丁基取代基的水凝胶在 2 天内完全降解。新的水凝胶材料也被证明与 hMSCs 具有生物相容性,并且细胞释放动力学可以在 5 天内轻松调节。