Ren Fangfang, Hua Mingming, Yang Zhijie, Wei Jingjing
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, PR China.
Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, PR China.
J Colloid Interface Sci. 2022 Sep;621:331-340. doi: 10.1016/j.jcis.2022.04.027. Epub 2022 Apr 9.
Although it is well-accepted that iron oxide nanoparticles are considered as artificial enzymes when their surface is hydrophilic, the enzyme-like properties of iron oxide nanoparticles with hydrophobic surface coating is unexplored. This work demonstrates that hydrophobic iron oxide nanocrystals coated with a layer of oleic acid could serve as artificial enzymes when their surface is covered by a layer of ionic surfactant. Furthermore, the co-assembly of iron oxide nanocrystals and porous organic cages could modulate their enzyme-like activities.
Co-assembly of iron oxide (FeO) nanocrystals with different size and porous organic cages (POCs) was performed by an emulsion-confined strategy to achieve hybridized FeO/POCs co-assemblies. The peroxidase-mimic activity of these co-assemblies were assessed in the presence of 3, 3', 5, 5'-Tetramethylbenzidine (TMB) and hydrogen peroxide. Finally, these co-assemblies were applied as sensors to detect glucose and hydrogen peroxide.
Co-assembly of FeO nanocrystals and POCs resulted in the self-assembly of FeO nanoparticles into two-dimensional nanoparticle superlattices on the eight (111) facets of the octahedral POCs colloidal crystals. The unique oil-in-water (O/W) emulsion confined assembly method switches the FeO nanoparticles and POC crystals from hydrophobic to hydrophilic because of the strong hydrophobic interactions. Importantly, these co-assemblies dispersed in water showed strong peroxidase-mimic activity in water despite that their surface is covered by a bilayer of aliphatic chains. Furthermore, the intrinsic enzymatic activity of the co-assemblies is highly dependent on the size of the nanocrystals, and a higher catalytic activity is achieved from a larger sized FeO nanocrystal.
尽管人们普遍认为当氧化铁纳米颗粒表面具有亲水性时可被视为人工酶,但具有疏水表面涂层的氧化铁纳米颗粒的类酶性质尚未得到探索。这项工作表明,包覆有一层油酸的疏水氧化铁纳米晶体在其表面被一层离子表面活性剂覆盖时可作为人工酶。此外,氧化铁纳米晶体与多孔有机笼的共组装可以调节它们的类酶活性。
采用乳液受限策略进行不同尺寸的氧化铁(FeO)纳米晶体与多孔有机笼(POC)的共组装,以实现FeO/POC杂化共组装体。在3,3',5,5'-四甲基联苯胺(TMB)和过氧化氢存在的情况下评估这些共组装体的过氧化物酶模拟活性。最后,将这些共组装体用作传感器来检测葡萄糖和过氧化氢。
FeO纳米晶体与POC的共组装导致FeO纳米颗粒在八面体POC胶体晶体的八个(111)晶面上自组装成二维纳米颗粒超晶格。独特的水包油(O/W)乳液受限组装方法由于强烈的疏水相互作用,将FeO纳米颗粒和POC晶体从疏水性转变为亲水性。重要的是,尽管这些共组装体的表面被脂肪族链双层覆盖,但分散在水中时仍在水中表现出强烈的过氧化物酶模拟活性。此外,共组装体的固有酶活性高度依赖于纳米晶体的尺寸,较大尺寸的FeO纳米晶体具有更高的催化活性。