Faculty of Life Science and Technology, Kunming University of Science and Technology, Yunnan Province, 650500, China.
Mikrochim Acta. 2024 Sep 17;191(10):604. doi: 10.1007/s00604-024-06684-8.
An oxidase (OXD) -like AuAg@AuNPs nanozyme was prepared by Au seeds growth using dopamine carbon dots as reducing and capping agents. The AuAg@AuNPs show excellent OXD-like and surface-enhanced Raman spectroscopy (SERS) activities and can oxidize the non-Raman-active leucomalachite green (LMG) into the Raman-active malachite green (MG). The research displays that D-penicillamine (D-PA) can effectively inhibit the OXD-like activity of Au@AgNPs and enhance the SERS signals as substrate. It is attributed to the formation of S-Au bond due to thiol (-SH) in D-PA. Therefore, a highly sensitive and specific SERS dual-readout sensing platform was proposed to assay D-PA with a limit of detection of 0.1 μg/mL (direct SERS mode) and 6.64 μg/L (indirect SERS mode). This approach was successfully used to determine D-PA in actual pharmaceutical formulations.
一种氧化酶(OXD)样的 AuAg@AuNPs 纳米酶是通过多巴胺碳点作为还原剂和稳定剂来制备的。AuAg@AuNPs 表现出优异的 OXD 样和表面增强拉曼光谱(SERS)活性,可以将非拉曼活性的隐色孔雀石绿(LMG)氧化为拉曼活性的孔雀石绿(MG)。研究表明,D-青霉胺(D-PA)可以有效抑制 Au@AgNPs 的 OXD 样活性,并作为基底增强 SERS 信号。这归因于 D-PA 中的巯基(-SH)形成了 S-Au 键。因此,提出了一种高灵敏度和特异性的 SERS 双读取传感平台,用于测定 D-PA,其检测限为 0.1μg/mL(直接 SERS 模式)和 6.64μg/L(间接 SERS 模式)。该方法成功用于测定实际药物制剂中的 D-PA。