Department of Biomedical Engineering, Purdue School of Engineering and Technology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Acta Biomater. 2014 Jan;10(1):104-14. doi: 10.1016/j.actbio.2013.08.044. Epub 2013 Sep 8.
We report here a synthetically simple yet highly tunable and diverse visible light mediated thiol-vinyl gelation system for fabricating cell-instructive hydrogels. Gelation was achieved via a mixed-mode step-and-chain-growth photopolymerization using functionalized 4-arm poly(ethylene glycol) as backbone macromer, eosin-Y as photosensitizer, and di-thiol containing molecule as dual purpose co-initiator/cross-linker. N-vinylpyrrolidone (NVP) was used to accelerate gelation kinetics and to adjust the stiffness of the hydrogels. Visible light (wavelength: 400-700 nm) was used to initiate rapid gelation (gel points: ~20s) that reached completion within a few minutes. The major differences between current thiol-vinyl gelation and prior visible light mediated photopolymerization are that: (1) the co-initiator triethanolamine (TEA) used in the previous systems was replaced with multifunctional thiols and (2) mixed-mode polymerized gels contain less network heterogeneity. The gelation kinetics and gel properties at the same PEG macromer concentration could be tuned by changing the identity of vinyl groups and di-thiol cross-linkers, as well as concentration of cross-linker and NVP. Specifically, acrylate-modified PEG afforded the fastest gelation rate, followed by acrylamide and methacrylate-functionalized PEG. Increasing NVP concentration also accelerated gelation and led to a higher network cross-linking density. Further, increasing di-thiol peptide concentration in the gel formulation increased hydrogel swelling and decreased gel stiffness. Due to the formation of thiol-ether-ester bonds following thiol-acrylate reaction, the gels degraded hydrolytically following a pseudo first order degradation kinetics. Degradation rate was controlled by adjusting thiol or NVP content in the polymer precursor solution. The cytocompatibility and utility of this hydrogel system were evaluated using in situ encapsulation of human mesenchymal stem cells (hMSC). Encapsulated hMSCs remained alive (>90%) throughout the duration of the study and the cells were differentiated down osteogenic lineage with varying degrees by controlling the rate and mode of gel degradation.
我们在此报告了一种合成简单但高度可调且多样化的可见光介导的巯基-乙烯基凝胶体系,用于制备具有细胞指令功能的水凝胶。凝胶化是通过使用功能化的 4 臂聚乙二醇(PEG)作为骨架大分子、曙红-Y 作为光敏剂、以及含二硫的分子作为双重用途的共引发剂/交联剂的混合模式逐步和链式聚合来实现的。N-乙烯基吡咯烷酮(NVP)用于加速凝胶化动力学并调节水凝胶的刚性。可见光(波长:400-700nm)用于引发快速凝胶化(凝胶点:~20s),几分钟内即可完成。目前的巯基-乙烯基凝胶化与之前的可见光介导光聚合的主要区别在于:(1)先前体系中使用的共引发剂三乙醇胺(TEA)被多功能硫醇取代,以及(2)混合模式聚合的凝胶中网络异质性较少。通过改变乙烯基基团和二硫交联剂的种类、交联剂和 NVP 的浓度,可以调节相同 PEG 大分子浓度下水凝胶的凝胶动力学和凝胶性能。具体而言,丙烯酸酯修饰的 PEG 赋予最快的凝胶化速率,其次是丙烯酰胺和甲基丙烯酸酯修饰的 PEG。增加 NVP 浓度也会加速凝胶化并导致更高的网络交联密度。此外,增加凝胶配方中二硫肽的浓度会增加水凝胶的溶胀并降低凝胶的刚性。由于巯基-丙烯酰反应后形成了巯基-醚-酯键,因此凝胶在水解作用下按照伪一级降解动力学进行降解。降解速率通过调节聚合物前体溶液中的巯基或 NVP 含量来控制。通过原位封装人骨髓间充质干细胞(hMSC)来评估该水凝胶体系的细胞相容性和实用性。在整个研究过程中,封装的 hMSC 保持存活(>90%),并且通过控制凝胶降解的速率和模式,细胞沿着成骨谱系以不同程度分化。