Highly selective nanozyme-based glucose sensing platform via construction of artificial recognition sites on gold nanospheres

单糖 分子印迹聚合物 葡萄糖氧化酶 选择性 化学 纳米技术 检出限 组合化学 硼酸 人工酶 生物传感器 催化作用 材料科学 色谱法 有机化学 生物化学
作者
Jinping Yu,Tao Chen,Xueyun Wen,Hao Shi,Lupeng Wang,Yuanhong Xu
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:253: 116169-116169 被引量:60
标识
DOI:10.1016/j.bios.2024.116169
摘要

Nanozymes have been regarded as the ideal alternatives to natural enzymes in bioassays due to their good stability and low cost. However, their applications in sensing usually suffer from poor selectivity. For example, Au-based nanozymes, as a kind of classical glucose oxidase mimic enzyme, could catalyze diverse monosaccharides. Therefore, it is of great necessity and urgency to endow the Au-based nanozymes with enhanced selectivity for the construction of specific glucose sensing platform. In our study, easily recyclable polydopamine (PDA)-supported Au-based nanozymes (PDA@Au NPs) were successfully prepared and could catalyze diverse monosaccharides including glucose, xylose, mannose, and sucrose. To enhance the selectivity of PDA@Au NPs, molecularly imprinted polymers (MIPs) were constructed on the surface of PDA@Au NPs using glucose and boronic acid derivatives as template and functional monomer. Impressively, the catalytic activity of the obtained molecularly imprinted nanozyme (PDA@Au NPs-MIPs) only shows a slight decrease (6.3%) while their selectivity is obviously enhanced (≥230%). Accordingly, the as-prepared sensor achieved the sensitive and selective detection of glucose in the concentration range of 10 μM-1 mM and a low detection limit (LOD) of 0.227 μM (S/N = 3), avoiding the influence of other monosaccharides exited in the sensing solutions to a great extent. As expected, the as-prepared sensors also showed good recovery, and long-term stability.
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