首页> 外文会议>Conference on Plasmonics in Biology and Medicine XVI >Towards development of fiber-optic surface enhanced Raman spectroscopy probes using 2-photon polymerization for rapid detection of bacteria
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Towards development of fiber-optic surface enhanced Raman spectroscopy probes using 2-photon polymerization for rapid detection of bacteria

机译:使用2-光子聚合进行纤维 - 光学表面增强的拉曼光谱探针,用于快速检测细菌的纤维 - 光学表面增强拉曼光谱探针

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In this study, a variety of direct laser written surface-enhanced Raman spectroscopy (SERS) micro-structures, designedfor bacteria detection, are presented. Various SERS micro-structures were designed to achieve both a high density ofplasmonic hot spots and a strong probability of interaction between the hot spots and the target bacterial cells. Twophotonpolymerization was used for initial fabrication of the polymeric skeletons of the SERS micro-structures, whichwere then coated with a 50 nm-thick gold layer via e-beam evaporation. The micro-structures were fabricated on glasscoverslips and were assessed using a confocal Raman microscope. To this end, Rhodamine 6G was used as an analyteunder 785 nm laser illumination. The optimal SERS micro-structures showed approximately 2×10~3 enhancement inRaman signal (analytical enhancement factor, AEF) at a wavenumber of 600 cm~(-1). Real-time detection of E. coli insolution was demonstrated using the fabricated SERS platform with low laser powers and a short acquisition time (785nm, 5 mW, 50 ms).
机译:在本研究中,各种直接激光书面表面增强拉曼光谱(SERS)微结构,设计对于细菌检测,呈现。设计各种SERS微结构,以实现高密度等离子体热点和热斑和靶细菌细胞之间的相互作用的强概率。叽叽喳喳聚合用于初始制造SERS微结构的聚合物骨架,然后通过电子束蒸发涂覆50nm厚的金层。微结构在玻璃上制造盖玻片并使用共焦拉曼显微镜进行评估。为此,罗丹明6g用作分析物在785 nm激光照射下。最佳SERS微结构显示出约2×10〜3的增强拉曼信号(分析增强因子,余地)在600cm〜(-1)的波数。大肠杆菌的实时检测使用具有低激光功率的制造的SERS平台和短采集时间(785NM,5 MW,50毫秒)。

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