College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai, 201620, People's Republic of China.
College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, 2999 North Renmin Road, Shanghai, 201620, People's Republic of China.
Mikrochim Acta. 2019 Apr 8;186(5):271. doi: 10.1007/s00604-019-3395-8.
A method is described for the preparation of copper(II)-modified keratin-capped gold nanoclusters (AuNCs) with adjustable Au/Cu molar ratio through a two-step synthetic route. The introduction of Cu(II) is known to cause quenching of the fluorescence of such AuNCs. It is found, however, that the Cu(II) loaded AuNC (AuNC-Cu) display strongly enhanced peroxidase-like activity and improved chemical stability. This is assumed to be due to the synergistic effect of the gold and copper atoms and in contrast to the single components (pure AuNCs and copper ions). The kinetic parameters of the new peroxidase mimic show a higher K value (12.1 × 10 s) and a lower K value (53 μM) for HO (compared to those of conventional AuNCs). The catalytic activity is stable and remains essentially unchanged after two months. The interactions of AuNCs with Cu(II) were characterized by fluorescence spectroscopy, UV-vis spectroscopy and X-ray photoelectron spectroscopy. Based on these findings, a glucose colorimetric assay at 452 nm was developed that has a detection range from 1.6 to 800 μM and a 0.26 μM detection limit. Graphical abstract Copper ion-modified keratin-capped gold nanoclusters (AuNC-Cu) exhibit enhanced peroxidase-like activity owing to the synergistic effect of the gold and copper atoms which is in contrast to pure AuNCs.
一种通过两步合成路线制备具有可调 Au/Cu 摩尔比的铜(II)修饰角蛋白覆盖的金纳米团簇(AuNCs)的方法。已知 Cu(II)的引入会猝灭此类 AuNC 的荧光。然而,发现负载 Cu(II)的 AuNC(AuNC-Cu)显示出增强的过氧化物酶样活性和提高的化学稳定性。这被认为是由于金和铜原子的协同效应,与单一成分(纯 AuNCs 和铜离子)形成对比。这种新型过氧化物酶模拟物的动力学参数显示出更高的 K 值(12.1×10 s)和更低的 K 值(53 μM),用于 HO(与常规 AuNCs 相比)。催化活性稳定,两个月后基本保持不变。通过荧光光谱、紫外可见光谱和 X 射线光电子能谱对 AuNCs 与 Cu(II) 的相互作用进行了表征。基于这些发现,开发了一种在 452nm 处的葡萄糖比色测定法,其检测范围为 1.6 至 800 μM,检测限为 0.26 μM。