Centre for Advanced Materials, Indian Association for the Cultivation of Science, Kolkata 700032, India.
Anal Chem. 2013 Oct 1;85(19):9221-8. doi: 10.1021/ac4019457. Epub 2013 Sep 13.
Glutathione (GSH) and oxidized glutathione (GSSG) control cellular function and efficiency of anticancer therapy. Reliable detection of cellular GSH/GSSG is challenging due to their ultralow concentration (typically femtomolar concentrations) and interference by other thiol-based molecules. Here, we report a "turn-off" surface enhanced Raman scattering (SERS)-based approach for reliable detection of cellular GSH and GSSG. This approach exploits GSH-induced replacement of a Raman probe from the surface of γ-Fe2O3-Au followed by Ag growth around γ-Fe2O3-Au that generates electromagnetic hot spots at the junction between Au and Ag where the Raman probe is localized. The magnetic component of the hybrid nanoparticle concentrates the cellular GSH, and the Au/Ag-based plasmonic component provides electromagnetic hot spots for sensitive SERS. This approach is able to monitor GSH level during photothermal cancer therapy.
谷胱甘肽 (GSH) 和氧化型谷胱甘肽 (GSSG) 控制着细胞的功能和抗癌治疗的效率。由于其超低浓度(通常为飞摩尔浓度)以及其他含巯基分子的干扰,可靠检测细胞内 GSH/GSSG 具有挑战性。在这里,我们报告了一种基于“关闭”表面增强拉曼散射 (SERS) 的方法,用于可靠检测细胞内 GSH 和 GSSG。该方法利用 GSH 诱导从 γ-Fe2O3-Au 表面替换拉曼探针,然后在 γ-Fe2O3-Au 周围生长 Ag,在 Au 和 Ag 的交界处产生电磁热点,拉曼探针在该交界处定位。该杂交纳米颗粒的磁性部分浓缩了细胞内的 GSH,而基于 Au/Ag 的等离子体部分则为敏感的 SERS 提供了电磁热点。该方法能够在光热癌症治疗过程中监测 GSH 水平。