DWI-Leibniz Institute for Interactive Materials, Forckenbeckstrasse 50, 52056 Aachen (Germany) http://www.dwi.rwth-aachen.de.
Angew Chem Int Ed Engl. 2015 Nov 2;54(45):13258-62. doi: 10.1002/anie.201505013. Epub 2015 Aug 6.
Switchable self-assemblies respond to external stimuli with a transition between near-equilibrium states. Although being a key to present-day advanced materials, these systems respond rather passively, and do not display autonomous dynamics. For autonomous behavior, approaches must be found to orchestrate the time domain of self-assemblies, which would lead to new generations of dynamic and self-regulating materials. Herein, we demonstrate catalytic control of the time domain of pH-responsive peptide hydrogelators in a closed system. We program transient acidic pH states by combining a fast acidic activator with the slow, enzymatic, feedback-driven generation of a base (dormant deactivator). This transient state can be programmed over orders of magnitude in time. It is coupled to dipeptides to create autonomously self-regulating, dynamic gels with programmed lifetimes, which are used for fluidic guidance, burst release, and self-erasing rapid prototyping.
可切换的自组装体通过在近平衡状态之间的转变对外界刺激做出响应。尽管这些系统是当今先进材料的关键,但它们的响应相当被动,并且不显示自主动力学。为了实现自主行为,必须找到方法来协调自组装体的时间域,这将导致新一代动态和自我调节材料的出现。在这里,我们证明了在封闭系统中通过组合快速酸性激活剂和缓慢的酶促反馈驱动的碱(休眠失活剂)生成来控制 pH 响应肽水凝胶形成剂的时间域的催化控制。我们通过将二肽与瞬时酸性 pH 状态偶联来创建具有编程寿命的自主自我调节的动态凝胶,这些凝胶可用于流体制导、爆发释放和自我擦除快速原型制作。