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Gold nanorods for cell imaging with confocal reflectance microscopy and two-photon fluorescence microscopy

机译:共聚焦反射显微镜和双光子荧光显微镜用于细胞成像的金纳米棒

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Gold nanorods have unique optical properties as their two photon absorption cross sections are very high and their spectral positions of extinction bands can be controlled by their aspect ratio only, so that gold nanorods have been considered as agents for cell imaging. Two-photon photoluminescence imaging could be used to detect the cellular gold nanorods with the high power femto-second (fs) infrared laser, but may cause the photothermal effect melting the rods. The 3-D distribution of gold nanorods in living cells also can be measured by confocal reflectance microscopy with a very low laser power, and thus the cell damaging can be avoided. In this work, these two methods were comparatively studied in living rat basophilic leukemia (RBL-2H3) cells.
机译:金纳米棒具有独特的光学特性,因为它们的两个光子吸收截面非常高,并且消光带的光谱位置只能通过其长宽比来控制,因此金纳米棒被视为细胞成像的试剂。双光子光致发光成像可用于通过高功率飞秒(fs)红外激光检测蜂窝状金纳米棒,但可能导致光热效应熔化棒。金纳米棒在活细胞中的3-D分布也可以通过共聚焦反射显微镜以非常低的激光功率进行测量,因此可以避免细胞损伤。在这项工作中,这两种方法在活大鼠嗜碱性粒细胞白血病(RBL-2H3)细胞中进行了比较研究。

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