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Nonlinear Optical Properties of Gold Nanorods (GNRs) under FS Laser Excitation near the Third Optical Tissue Window and Application for Multichannel Cellular Imaging

机译:第三光学组织窗口附近FS激光激发下的金纳米棒(GNRS)的非线性光学性质及多通道蜂窝成像的应用

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Gold nanorod (GNR) was a promising bioimaging probe in the third optical tissue window (1600-1800 nm). In this paper, hydrophilic GNRs with proper dimensions were synthesized according to the classical seed mediated method. Their nanostructures were taken with a transmission electron microscope and their extinction spectra were recorded on a UV-vis scanning spectrophotometer. Their nonlinear optical features were recorded by a home built measurement system, under the femtosecond (fs) laser excitation of 1580 nm, which was selected as the demonstration of the third optical tissue window. A sharp third harmonic generation (THG) signal and a mild three photon luminescence (3PL) signal could be clearly distinguished. These signals could be utilized for multichannel nonlinear bioimaging in the third optical tissue window. Negatively charged polystyrene sulfonate (PSS) and positively charged polyallylamine hydrochloride (PAH) were separately coated onto the positively charged GNRs through electrostatic adherence. The PAH-PSS coated GNRs were added in the culture medium of HeLa cells. Multichannel nonlinear optical imaging of cancer cells stained with GNRs was performed with a 1580 nm fs laser coupled scanning microscope. The signals were filtered by a 665 nm dichroic mirror, and then splitted by another 560 nm dichroic mirror into the green and red imaging channels. HeLa cells can be clearly visualized in both green and red channels with good contrast. For HeLa cells without GNRs treatment, there were no such signals detected in these channels. This was a pioneer work of the multichannel nonlinear bioimaging in the third optical tissue window with GNRs and would be helpful for our further studies on in vivo bioimaging in this window with deeper penetration.
机译:金纳米棒(GNR)是第三光学组织窗口(1600-1800nm)的有前途的生物影像探针。在本文中,根据经典的种子介导的方法合成具有适当尺寸的亲水GNR。它们的纳米结构用透射电子显微镜拍摄,并且它们的消光光谱被记录在UV-Vis扫描分光光度计上。它们的非线性光学特征由家庭建造的测量系统记录,在1580nm的飞秒(FS)激光激发下,选择为第三光学组织窗口的演示。可以清楚地区分尖锐的三次谐波产生(THG)信号和温和的三个光子发光(3pl)信号。这些信号可用于第三光学组织窗口中的多通道非线性生物分析。带负电的聚苯乙烯磺酸盐(PSS)和带正电荷的聚烯丙胺盐酸盐(PAH)通过静电粘附分别涂覆到正电荷的GNR上。在HeLa细胞的培养基中加入PAH-PSS涂覆的GNR。用1580nm FS激光耦合扫描显微镜进行用GNR染色的癌细胞的多通道非线性光学成像。信号通过665nm二向色镜过滤,然后通过另一个560nm二向色镜分离成绿色和红色成像通道。 Hela细胞可以在绿色和红色通道中清晰可视化,具有良好的对比度。对于没有GNR处理的Hela细胞,在这些通道中没有检测到这样的信号。这是具有GNR的第三光学组织窗口中的多通道非线性生物成像的先驱工作,并且有助于我们进一步研究该窗口中的体内生物成像,深入渗透。

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