School of Pharmacy, Shanxi Medical University, Taiyuan, 030001, China.
Mikrochim Acta. 2024 Feb 16;191(3):140. doi: 10.1007/s00604-023-06167-2.
A sandwich-structured composite nanoenzyme (NH-MIL-101(Fe)@Au@MIP) was prepared using molecularly imprinted polymers, metal-organic frameworks, and gold nanoparticles and a highly selective glutathione (GSH) colorimetric sensor was constructed. The inner part of the composite nanoenzymes is a metal-organic framework loaded with gold nanoparticles (AuNPs), NH-MIL-101(Fe)@Au, which has superior peroxidase-like activity compared with NH-MIL-101(Fe). This is due to the surface plasmon resonance effect of AuNPs. GSH can form strong Au-S bonds with AuNPs, which can significantly reduce the enzymatic activity of NH-MIL-101(Fe)@Au, thereby changing the absorbance at 450 nm of the sensing system. The degree of change in absorbance is correlated with the concentration of GSH. In the outer part, the molecularly imprinted polymer with oxidized glutathione (GSSG) as a dummy template provided specific pores, which significantly improved the selectivity of the sensing system. The sensor showed good GSH sensing performance in the range 1 ~ 50 μM with a lower limit of detection (LOD) of 0.231 μM and good sensing performance in fetal bovine serum, indicating its high potential for clinical diagnostic applications.
采用分子印迹聚合物、金属有机骨架和金纳米粒子制备了一种三明治结构的复合纳米酶(NH-MIL-101(Fe)@Au@MIP),构建了一种高选择性谷胱甘肽(GSH)比色传感器。该复合纳米酶的内部为负载金纳米粒子(AuNPs)的金属有机骨架(NH-MIL-101(Fe)@Au),其过氧化物酶样活性明显优于 NH-MIL-101(Fe)。这是由于 AuNPs 的表面等离子体共振效应。GSH 可以与 AuNPs 形成强的 Au-S 键,从而显著降低 NH-MIL-101(Fe)@Au 的酶活性,从而改变传感系统在 450nm 处的吸光度。吸光度的变化程度与 GSH 的浓度相关。在外部,以氧化型谷胱甘肽(GSSG)为虚拟模板的分子印迹聚合物提供了特定的孔道,显著提高了传感系统的选择性。该传感器在 1μM 至 50μM 的范围内表现出良好的 GSH 传感性能,检测限(LOD)低至 0.231μM,在胎牛血清中具有良好的传感性能,表明其在临床诊断应用中具有很高的潜力。