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基于普鲁士蓝包覆的金纳米双锥体的背景自由 SERS 纳米传感器用于内源性硫化氢检测。

Background-Free SERS Nanosensor for Endogenous Hydrogen Sulfide Detection Based on Prussian Blue-Coated Gold Nanobipyramids.

机构信息

Department of Laboratory Medicine, Xiamen Key Laboratory of Genetic Testing, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen 361005, People's Republic of China.

Ministry of Education Key Laboratory for Analytical Science of Food Safety and Biology, Fujian Provincial Key Laboratory of Analysis and Detection for Food Safety, Department of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2024 Mar 27;16(12):14467-14473. doi: 10.1021/acsami.3c17385. Epub 2024 Mar 16.

Abstract

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 HS detection. The PB shell degraded quickly upon contact with endogenous HS, generating a unique Raman signal response in the Raman silent region (1800-2800 cm). By taking advantage of the high SERS-activity of Au NBPs and HS-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 HS concentrations in human serum samples with satisfied results.

摘要

表面增强拉曼散射(SERS)由于其特异性、灵敏度和非侵入性,在生物分析中具有很大的潜力。然而,有效地提取拉曼信息并避免生物背景干扰的光谱重叠仍然是主要挑战。在这项研究中,我们开发了一种由金纳米双锥体(Au NBPs)核-普鲁士蓝(PB)壳(Au NBPs@PB)组成的无背景 SERS 纳米传感器,用于内源性 HS 的检测。PB 壳与内源性 HS 接触后迅速降解,在拉曼静默区(1800-2800cm)产生独特的拉曼信号响应。利用 Au NBPs 的高 SERS 活性和 HS 触发的 PB 光谱变化,这些 SERS 纳米传感器有效地最小化了潜在的生物干扰。该纳米传感器的检测范围为 2.0 μM 至 250 μM,检测限(LOD)为 0.34 μM,具有良好的重现性和最小的干扰。我们成功地应用这种无背景 SERS 平台来监测人血清样本中的内源性 HS 浓度,结果令人满意。

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