Ag nanoparticle-modified porous nickel foam nanotemplate: An efficient surface-enhanced Raman scattering platform for the rapid detection of artemisinin

拉曼散射 材料科学 基质(水族馆) 拉曼光谱 检出限 溅射沉积 溅射 纳米颗粒 纳米技术 薄膜 化学 色谱法 光学 海洋学 物理 地质学
作者
Wenzhi Yuan,Zhibin Zhang,Yanjun Wu,Guochao Shi,Shiqi Xu
出处
期刊:AIP Advances [American Institute of Physics]
卷期号:12 (10) 被引量:4
标识
DOI:10.1063/5.0101873
摘要

Because of the advantages of rapid sampling and real-time detection, the surface-enhanced Raman scattering (SERS) technique provides greater potential for ultrasensitive detection of active components in traditional Chinese medicine. In this paper, an ultrasensitive SERS detection system was successfully designed using controllable magnetron sputtering technology for the rapid and quantitative detection of artemisinin, a traditional Chinese medicine. Using nickel foam (NF) with a three-dimensional porous mesh structure as a template, Ag nanoparticle layers were sputtered on the NF surface by the magnetron sputtering technique to prepare Ag-NF-20 (the magnetron sputtering time was 20 min) SERS substrates with high SERS performance. According to the SERS signal response of the R6G molecule on the Ag-NF-20 substrate, this efficient SERS platform showed excellent Raman signals and enhanced performance and time-stability. The results suggested that owing to the abundant electromagnetic enhancement “hot spots” distributed on Ag-NF-20 nanostructures, an experimental enhancement factor value of 6.57 × 105 was obtained. The time-stability for 30 days in an atmospheric environment was also determined, which revealed that a minimum decrease of 2.6% in Raman signal intensity was recorded, indicating the excellent time-stability of the Ag-NF-20 substrate. Furthermore, when applying this in the detection of artemisinin, the limit of detection value for artemisinin was 1 × 10−4 ng/ml. Therefore, the Ag-NF-20 SERS substrate has great potential for trace detection of other active ingredients in traditional Chinese medicine and is expected to expand the detection of pharmacodynamic substances in clinical drugs.

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