Antibiotics Research and Re-Evaluation Key Laboratory of Sichuan Province, Chengdu University, Chengdu, 610106, China.
Key Laboratory of Medicinal and Edible Plants Resources Development of Sichuan Education Department, Chengdu University, Chengdu, 610106, China.
Mikrochim Acta. 2022 Mar 29;189(4):162. doi: 10.1007/s00604-022-05268-8.
Fe-based metal-organic framework (MIL-101(Fe)) was synthesized through a simple solvothermal synthesis and then used to prepare the AuNPs-decorated MIL-101(Fe) nanocomposite (APPPM(Fe)) by a multi-step layer-by-layer assembly process. Benefited from the porous structure of MIL-101(Fe) and the multilayer assemble process, the loading amount of AuNPs on APPPM(Fe) was enhanced and exhibited a fine biocompatible interface and high conductivity. Through the intense Au-S bond, high loading amount of horseradish peroxidase was immobilized on APPPM(Fe) and the native bioactivity of HRP was kept to realize its direct electrochemistry. From the electrochemical kinetics, the constructed biosensor displayed fast electron transfer and good electrocatalysis activity for the detection of nitric oxide (NO) with wide linear range from 0.033 to 5370 μM and a low detection limit of 0.01 μM (3 σ) as well as fine stability, reproducibility and specificity. According to results of real sample analysis, the proposed electrochemical biosensor offers fast and simple detection of NO in real serum. Therefore, the present strategy definitely provided a potential application prospect in NO clinic detection and disease therapy.
通过简单的溶剂热合成合成了基于铁的金属有机骨架(MIL-101(Fe)),然后通过多步层层组装过程将其用于制备 AuNPs 修饰的 MIL-101(Fe)纳米复合材料(APPPM(Fe))。受益于 MIL-101(Fe)的多孔结构和多层组装过程,APPPM(Fe)上 AuNPs 的负载量增加,并表现出精细的生物相容性界面和高导电性。通过强烈的 Au-S 键,辣根过氧化物酶(HRP)被固定在 APPPM(Fe)上,并且保持 HRP 的天然生物活性,以实现其直接电化学。从电化学动力学来看,构建的生物传感器对一氧化氮(NO)的检测具有快速的电子转移和良好的电催化活性,线性范围从 0.033 到 5370 μM,检测限低至 0.01 μM(3 σ),并且具有良好的稳定性、重现性和特异性。根据实际样品分析结果,该电化学生物传感器可用于快速简便地检测实际血清中的 NO。因此,本研究策略在 NO 的临床检测和疾病治疗方面具有潜在的应用前景。