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Facile strategy to prepare a metalloporphyrin-based hydrophilic porous organic polymer with enhanced peroxidase-like activity and high stability for colorimetric detection of H2O2 and glucose

机译:通过增强过氧化物酶样活性的制备金属卟啉基亲水多孔有机聚合物的容易策略,H2O2和葡萄糖的比例检测高稳定性

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Nanozymes, nanomaterial-based artificial enzymes, have attracted researchers' enormous interest due to their unique properties compared with natural enzymes. To mimic the catalytic function of natural enzymes, designing high-efficient, novel nanozymes is crucial yet challenging task. In this article, we described the synthesis and functions of a metalloporphyrin-based porous organic polymer, namely FePPOPs-SO3H. FePPOPs-SO3H was synthesized effortlessly via an extensive aromatic electrophilic substitution and the following sulfonation reactions. This strategy was cost-efficient without the participation of precious metal catalysts. The resultant FePPOPs-SO3H is intriguing since the framework itself is constructed by covalently linked porphyrin units, which could serve as a built-in catalyst and strengthen the stability of polymer. With sulfonic acid side groups, FePPOPs-SO3H is well water-dispersive. Owing to these unique characteristics, FePPOPs-SO3H exhibited excellent peroxidase-like activity toward a classical peroxidase substrate 3,3',5,5'-tetramethylbenzidine (TMB) to produce a blue product only within 20 s. The peroxidase-mimicking performance of FePPOPs-SO3H outperforms the ferric porphyrin monomer and normal Fe3O4 nanoparticles. Based on the excellent catalytic activity of FePPOPs-SO3H, two visual colorimetric sensors for ultrafast detecting H2O2 and glucose, respectively, were constructed with a wide linear range of 50-1800 mu M (for H2O2) and 200-1500 mu M (for glucose), as well as a relative lower limit of detection (LOD) [26.70 mu M (for H2O2) and 16.38 mu M (for glucose)]. Our strategy highlights opportunities for the design of new metalloporphyrin-based porous organic polymers with built-in catalytic skeletons and inherently excellent peroxidase-mimicking performance.
机译:纳佐中,基于纳米材料的人工酶,由于与天然酶相比,由于其独特的特性引起了研究人员的巨大兴趣。为了模仿天然酶的催化功能,设计高效,新型纳米酶至关重要但具有挑战性的任务。在本文中,我们描述了金属卟啉基多孔有机聚合物的合成和功能,即FEPPOPS-SO3H。通过广泛的芳族亲电子取代和以下磺化反应轻松地毫不含糊地合成FEPPOPS-SO3H。没有贵金属催化剂的参与,这种策略具有成本效益。得到的FEPPOPS-SO3H是有趣的,因为框架本身由共价连接的卟啉单位构成,其可以用作内置催化剂并强化聚合物的稳定性。用磺酸侧基团,FEPPOPS-SO3H是井水分散的。由于这些独特的特性,FEPPOPS-SO3H朝向经典过氧化物酶基质3,3',5,5'-四甲基苯甲酸(TMB)的优异过氧化物酶样活性表现出在20秒内仅制备蓝产物。 FEPPOPS-SO3H的过氧化物酶模拟性能优于铁卟啉单体和正常Fe3O4纳米粒子。基于FEPPOPS-SO3H的优异催化活性,分别构建了两个用于超快检测H2O2和葡萄糖的视觉比色传感器,其宽线性范围为50-1800μm(用于H2O2)和200-1500μm(用于葡萄糖),以及检测(LOD)的相对较低限度[26.70μm(对于H2O2)和16.38μm(用于葡萄糖)]。我们的战略凸显了具有内置催化骨架的新型金属卟啉的多孔有机聚合物的机会,具有固有的优异过氧化物酶模拟性能。

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