Huang Zhicheng, Liu Biwu, Liu Juewen
Department of Chemistry, Waterloo Institute for Nanotechnology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Nanoscale. 2020 Nov 28;12(44):22467-22472. doi: 10.1039/d0nr07055f. Epub 2020 Nov 5.
Using citrate-capped gold nanoparticles (AuNPs) as peroxidase-mimicking enzymes to design biosensors is hindered by their low catalytic activity and poor colloidal stability, resulting in limited sensitivity and large variations. Herein, the growth of a partial iron phosphate (FeP) shell with Fe ions on citrate-capped AuNPs boosted the activity of the AuNPs by up to 20-fold. The FeP-enhanced activity was demonstrated on AuNPs of different sizes, and gold nanostars. When the FeP layer is thick enough to block the access to the Au/FeP interface, the activity was inhibited. Capping the remaining Au surface by thiol also inhibited the activity, suggesting that faster reactions occurred at the interfaces of Au/FeP. Moreover, a FeP shell can stabilize AuNPs against freezing and a high NaCl concentration of 1 M. Sensitive detection of Fe was achieved with a detection limit of 0.41 μM, while no other tested transition metal phosphates enhanced the peroxidase-like activity of AuNPs.
使用柠檬酸盐包覆的金纳米颗粒(AuNP)作为模拟过氧化物酶来设计生物传感器,受到其催化活性低和胶体稳定性差的阻碍,导致灵敏度有限且变化很大。在此,在柠檬酸盐包覆的AuNP上生长带有铁离子的部分磷酸铁(FeP)壳层,使AuNP的活性提高了20倍。不同尺寸的AuNP和金纳米星上均证实了FeP增强的活性。当FeP层足够厚以阻止进入Au/FeP界面时,活性受到抑制。用硫醇覆盖剩余的Au表面也抑制了活性,这表明在Au/FeP界面发生了更快的反应。此外,FeP壳层可以使AuNP在冷冻和1 M的高NaCl浓度下保持稳定。实现了对铁的灵敏检测,检测限为0.41 μM,而其他测试的过渡金属磷酸盐均未增强AuNP的过氧化物酶样活性。