Institute of Functional Interfaces , Karlsruhe Institute of Technology , Hermann-von Helmholtz-Platz 1 , D-76344 Eggenstein-Leopoldshafen , Germany.
Institute for Organic Chemistry , Karlsruhe Institute of Technology , Fritz-Haber-Weg 6 , D-76131 Karlsruhe , Germany.
Acc Chem Res. 2019 Jun 18;52(6):1598-1610. doi: 10.1021/acs.accounts.9b00039. Epub 2019 Apr 12.
The integration of a porous crystalline framework with soft polymers to create novel biomaterials has tremendous potential yet remains very challenging to date. Metal-organic framework (MOF)-templated polymers (MTPs) have emerged as persistent modular materials that can be tailored for desired biofunctions. These represent a novel class of hierarchically structured assemblies that combine the advantages of MOFs (precisely controlled structure, enormous diversity in framework topology, and high porosity) with the intrinsic behaviors of polymers (soft texture, flexibility, biocompatibility, and improved stability under physiological conditions). Transformation of surface-anchored MOFs (SURMOFs) via orthogonal covalent cross-linking yields surface-anchored polymeric gels (SURGELs) that open up exciting new opportunities to create soft nanoporous materials. SURGELs overcome the main drawbacks of SURMOFs, such as their limited stability under physiological conditions and their potential to release toxic metal ions, a substantial problem for applications in life sciences. MOF (SURMOF)-templated polymerization processes control the synthesis on a molecular level. Additionally, the morphology of the original MOF crystal template is replicated in the final network polymers. The MOF-templated polymerization can be induced by light, a catalyst, or temperature using several types of reactions, including thiol-ene, metal-free alkyne-azide click reactions, and Glaser-Hay coupling. In the case of photoinduced reactions, the cross-linking process can be locally confined, allowing control of the macroscopic patterning of the resulting network polymer. The use of layer-by-layer (lbl) techniques in the SURMOF synthesis serves the purpose of precise, layer-selective incorporation of functionalities via the combination of the postsynthetic modification and heteroepitaxy strategies. Transforming the functionalized SURMOF into a SURGEL allows the fabrication of polymers with desired bioactive functions at the internal or external surfaces. This Account highlights our ongoing research and inspiring progress in transforming SURMOFs into persistent, modular nanoporous materials tailored with biofunctions. Using cell culture studies, we present various aspects of SURGEL materials, such as the ability to deliver bioactive molecules to adhering cells on SURGEL surfaces, applications to advanced drug delivery systems, the ability to tune cell adhesion via surface modification, and the development of porphyrin-based SURGEL thin films with antimicrobial properties. Then we critically examine the challenges and limitations of current systems and discuss future research directions and new approaches for advancing MOF-templated biocompatible materials, emphasizing the need to include responsive and adaptive functionalities into the system. We emphasize that the hierarchical structure, ranging from the molecular to the macroscopic scale, allows for optimization of the material properties across all length scales relevant for cell-material interactions.
将多孔晶体骨架与软聚合物集成以创建新型生物材料具有巨大的潜力,但迄今为止仍然极具挑战性。金属有机骨架(MOF)模板聚合物(MTP)已成为持久的模块化材料,可以针对所需的生物功能进行定制。这些材料代表了一类新型的分级结构组装体,结合了 MOF 的优点(精确控制结构,骨架拓扑结构的多样性以及高孔隙率)和聚合物的固有特性(柔软的质地,灵活性,生物相容性以及在生理条件下的稳定性提高)。通过正交共价交联对表面锚定的 MOF(SURMOF)进行转化,得到表面锚定的聚合物凝胶(SURGEL),这为创建软纳米多孔材料开辟了令人兴奋的新机会。SURGEL 克服了 SURMOF 的主要缺点,例如在生理条件下的稳定性有限以及释放有毒金属离子的潜在风险,这对生命科学中的应用是一个重大问题。MOF(SURMOF)模板聚合过程在分子水平上控制合成。此外,原始 MOF 晶体模板的形态在最终的网络聚合物中得到复制。MOF 模板聚合可以通过光,催化剂或温度使用几种类型的反应来引发,包括硫醇-烯,无金属炔基-叠氮点击反应和 Glaser-Hay 偶联。在光诱导反应的情况下,交联过程可以局部受限,从而可以控制所得网络聚合物的宏观图案化。在 SURMOF 合成中使用层层(lbl)技术的目的是通过组合后合成修饰和杂外延策略来精确,层选择地掺入功能。将功能化的 SURMOF 转化为 SURGEL 允许在内部或外部表面上制造具有所需生物活性功能的聚合物。本专题介绍了我们正在进行的研究工作,并介绍了将 SURMOF 转化为具有生物功能的持久模块化纳米多孔材料的令人鼓舞的进展。通过细胞培养研究,我们介绍了 SURGEL 材料的各个方面,例如将生物活性分子递送到 SURGEL 表面上附着的细胞的能力,在高级药物输送系统中的应用,通过表面修饰调节细胞粘附的能力以及基于卟啉的 SURGEL 薄膜的抗菌性能。然后,我们批判性地检查了当前系统的挑战和局限性,并讨论了推进 MOF 模板生物相容性材料的未来研究方向和新方法,强调需要将响应性和适应性功能纳入系统中。我们强调,从分子到宏观的层次结构允许优化与细胞-材料相互作用相关的所有长度尺度上的材料性能。