纳米传感器
普鲁士蓝
拉曼散射
拉曼光谱
材料科学
检出限
纳米技术
硫化氢
再现性
光学
化学
色谱法
电化学
电极
冶金
硫黄
物理化学
物理
作者
Jiaming Chen,Lingjun Cheng,Yuanyuan Yang,Yating Liu,Canping Su,Yinghao He,Mingming You,Zhenyu Lin,Guolin Hong
标识
DOI:10.1021/acsami.3c17385
摘要
Surface-enhanced Raman scattering (SERS) has great potential in biological analysis due to its specificity, sensitivity, and non-invasive nature. However, effectively extracting Raman information and avoiding spectral overlapping from biological background interference remain major challenges. In this study, we developed a background-free SERS nanosensor consisting of gold nanobipyramids (Au NBPs) core-Prussian blue (PB) shell (Au NBPs@PB), for endogenous H2S detection. The PB shell degraded quickly upon contact with endogenous H2S, generating a unique Raman signal response in the Raman silent region (1800–2800 cm–1). By taking advantage of the high SERS-activity of Au NBPs and H2S-triggered spectral changes of PB, these SERS nanosensors effectively minimize potential biological interferences. The nanosensor exhibits a detection range of 2.0 μM to 250 μM and a limit of detection (LOD) of 0.34 μM, with good reproducibility and minimal interference. We successfully applied this background-free SERS platform to monitor endogenous H2S concentrations in human serum samples with satisfied results.
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