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Surface-enhanced Raman spectroscopy and localized surface plasmon resonance detection of hydrogen peroxide using plasmonic gels

机译:使用等离子体胶的表面增强拉曼光谱和过氧化氢的局部表面等离子体共振检测

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摘要

We will present surface enhanced Raman spectroscopy (SERS) and localized surface plasmon resonance (LSPR)detection of hydrogen peroxide (H_2O_2) using plasmonic gels. It has been known that reactive oxygen species (ROS),such as hydrogen peroxide, are involved in various biological processes, including metabolism, cell signaling, proteinfolding, biosynthesis, and host defense. Therefore, developing a simple and sensitive method for monitoring ROS levelsis very important for live cell studies. Nevertheless, a challenge of utilizing SERS-based or LSPR-based method formolecular detection in complex fluids, such as cell culture media, is that a variety of molecules in sample solutions couldinterfere with detection results. In addition, when using SERS-based methods, the chance of having the target moleculesat the SERS hot spots is reduced when other molecules are present in the solution. To enable detection of H_2O_2 in cellculture media, we have developed SERS and LSPR detection methods based on gels containing plasmonic nanoparticles.Since gels are filter-like materials, H_2O_2 can penetrate through the gels, but cells and large molecules such as proteins areblocked. We have successfully utilized these two methods to detect H_2O_2 in cell culture media without any samplepretreatment.
机译:我们将介绍使用等离子凝胶的表面增强拉曼光谱(SERS)和局部表面等离振子共振(LSPR)\ r \ n检测过氧化氢(H_2O_2)。众所周知,活性氧(ROS),例如过氧化氢,参与了各种生物过程,包括新陈代谢,细胞信号传导,蛋白质折叠,生物合成和宿主防御。因此,开发一种简单而灵敏的方法来监测ROS水平对于活细胞研究非常重要。然而,利用基于SERS或LSPR的方法在复杂流体(例如细胞培养基)中进行分子检测的挑战在于,样品溶液中的多种分子可能会干扰检测结果。另外,当使用基于SERS的方法时,当溶液中存在其他分子时,降低了目标分子存在SERS热点的机会。为了能够检测细胞培养基中的H_2O_2,我们已经开发了基于包含等离激元纳米粒子的凝胶的SERS和LSPR检测方法。\ r \ n由于凝胶是滤膜状材料,H_2O_2可以穿透凝胶,但是细胞和大分子分子(例如蛋白质)被阻断。我们已经成功地利用了这两种方法来检测细胞培养基中的H_2O_2,而无需任何样品\ r \ n预处理。

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  • 来源
    《Plasmonics in Biology and Medicine XVI》|2019年|108940R.1-108940R.5|共5页
  • 会议地点 1605-7422;2410-9045
  • 作者单位

    Institute of Biophotonics, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei 11221, Taiwan (R.O.C.);

    Institute of Biophotonics, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei 11221, Taiwan (R.O.C.);

    Institute of Biophotonics, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei 11221, Taiwan (R.O.C.);

    Institute of Biophotonics, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei 11221, Taiwan (R.O.C.);

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