CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, Anhui Province, PR China.
Chem Soc Rev. 2012 Sep 21;41(18):5933-49. doi: 10.1039/c2cs35103j. Epub 2012 Jun 13.
Being responsive and adaptive to external stimuli is an intrinsic feature characteristic of all living organisms and soft matter. Specifically, responsive polymers can exhibit reversible or irreversible changes in chemical structures and/or physical properties in response to a specific signal input such as pH, temperature, ionic strength, light irradiation, mechanical force, electric and magnetic fields, and analyte of interest (e.g., ions, bioactive molecules, etc.) or an integration of them. The past decade has evidenced tremendous growth in the fundamental research of responsive polymers, and accordingly, diverse applications in fields ranging from drug or gene nanocarriers, imaging, diagnostics, smart actuators, adaptive coatings, to self-healing materials have been explored and suggested. Among a variety of external stimuli that have been utilized for the design of novel responsive polymers, enzymes have recently emerged to be a promising triggering motif. Enzyme-catalyzed reactions are highly selective and efficient toward specific substrates under mild conditions. They are involved in all biological and metabolic processes, serving as the prime protagonists in the chemistry of living organisms at a molecular level. The integration of enzyme-catalyzed reactions with responsive polymers can further broaden the design flexibility and scope of applications by endowing the latter with enhanced triggering specificity and selectivity. In this tutorial review, we describe recent developments concerning enzyme-responsive polymeric assemblies, nanoparticles, and hydrogels by highlighting this research area with selected literature reports. Three different types of systems, namely, enzyme-triggered self-assembly and aggregation of synthetic polymers, enzyme-driven disintegration and structural reorganization of polymeric assemblies and nanoparticles, and enzyme-triggered sol-to-gel and gel-to-sol transitions, are described. Their promising applications in drug controlled release, biocatalysis, imaging, sensing, and diagnostics are also discussed.
对外部刺激做出响应和适应是所有生物和软物质的固有特征。具体而言,响应性聚合物可以针对特定的信号输入(如 pH 值、温度、离子强度、光照射、机械力、电场和磁场以及感兴趣的分析物(例如离子、生物活性分子等)或它们的组合),表现出化学结构和/或物理性质的可逆或不可逆变化。在过去的十年中,响应性聚合物的基础研究取得了巨大的发展,因此,在药物或基因纳米载体、成像、诊断、智能执行器、自适应涂层、自修复材料等领域的各种应用已经得到了探索和提出。在用于设计新型响应性聚合物的各种外部刺激中,酶最近已成为一种很有前途的触发模式。在温和条件下,酶催化反应对特定底物具有高度的选择性和效率。它们参与所有的生物和代谢过程,作为生物体内分子水平上所有生命化学的主要参与者。通过赋予后者增强的触发特异性和选择性,将酶催化反应与响应性聚合物集成可以进一步拓宽后者的设计灵活性和应用范围。在本综述中,我们通过突出该研究领域的精选文献报道,描述了有关酶响应性聚合物组装体、纳米粒子和水凝胶的最新进展。描述了三种不同类型的系统,即合成聚合物的酶触发自组装和聚集、聚合物组装体和纳米粒子的酶驱动崩解和结构重组、以及酶触发溶胶-凝胶和凝胶-溶胶转变。还讨论了它们在药物控制释放、生物催化、成像、传感和诊断方面的有前景的应用。