Martini Maike, Hegger Patricia S, Schädel Nicole, Minsky Burcu B, Kirchhof Manuel, Scholl Sebastian, Southan Alexander, Tovar Günter E M, Boehm Heike, Laschat Sabine
Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, Stuttgart D-70569, Germany.
Department of Cellular Biophysics & CSF Biomaterials, Max-Planck Institute for Medical Research, Heidelberg D-69120, Germany.
Materials (Basel). 2016 Sep 30;9(10):810. doi: 10.3390/ma9100810.
Polyelectrolyte hydrogels play an important role in tissue engineering and can be produced from natural polymers, such as the glycosaminoglycan hyaluronan. In order to control charge density and mechanical properties of hyaluronan-based hydrogels, we developed cross-linkers with a neutral or positively charged triazole core with different lengths of spacer arms and two terminal maleimide groups. These cross-linkers react with thiolated hyaluronan in a fast, stoichiometric thio-Michael addition. Introducing a positive charge on the core of the cross-linker enabled us to compare hydrogels with the same interconnectivity, but a different charge density. Positively charged cross-linkers form stiffer hydrogels relatively independent of the size of the cross-linker, whereas neutral cross-linkers only form stable hydrogels at small spacer lengths. These novel cross-linkers provide a platform to tune the hydrogel network charge and thus the mechanical properties of the network. In addition, they might offer a wide range of applications especially in bioprinting for precise design of hydrogels.
聚电解质水凝胶在组织工程中发挥着重要作用,并且可以由天然聚合物制备,比如糖胺聚糖透明质酸。为了控制基于透明质酸的水凝胶的电荷密度和机械性能,我们开发了具有中性或带正电荷的三唑核心、不同长度间隔臂以及两个末端马来酰亚胺基团的交联剂。这些交联剂通过快速的化学计量硫醇-迈克尔加成反应与硫醇化透明质酸发生反应。在交联剂的核心引入正电荷使我们能够比较具有相同互连性但电荷密度不同的水凝胶。带正电荷的交联剂形成相对较硬的水凝胶,相对独立于交联剂的大小,而中性交联剂仅在小间隔长度时形成稳定的水凝胶。这些新型交联剂提供了一个调节水凝胶网络电荷从而调节网络机械性能的平台。此外,它们可能具有广泛的应用,特别是在生物打印中用于水凝胶的精确设计。