Advanced Photonics Center, Southeast University, Nanjing 210096, China.
Biosens Bioelectron. 2011 Feb 15;26(6):2883-9. doi: 10.1016/j.bios.2010.11.032. Epub 2010 Dec 1.
A dual-mode imaging probe for targeting cancer cells has been fabricated based on mesoporous silica coated gold nanorods (MS-GNRs) for the first time. In this probe, fluorescence and surface enhanced Raman scattering (SERS) signals can be generated independently by using different excitation wavelengths. To investigate the targeting performance of the probe, folic acid (FA) is conjugated on the outer surfaces of MS-GNRs as a targeting ligand and HeLa cells were used as model cancer cells because they overexpress folate receptors (FRs). The endocytosis mechanism was verified by competing experiments with free FA through both fluorescence images and SERS mappings. Moreover, the cytotoxicity of the probe was remarkably reduced in comparison with the GNRs without the silica shell as proved by the results of MTT assay. Compared with traditional imaging probes, this new type of nanoprobe has great potential for multiplexed imaging in living cells, which can be easily realized by using fluorescence and SERS signals.
一种双模成像探针已被首次研制出来,用于靶向癌细胞,该探针基于介孔硅包覆的金纳米棒(MS-GNRs)。在该探针中,荧光和表面增强拉曼散射(SERS)信号可以通过使用不同的激发波长独立产生。为了研究探针的靶向性能,将叶酸(FA)作为靶向配体接枝到 MS-GNRs 的外表面上,并且使用 HeLa 细胞作为模型癌细胞,因为它们过度表达叶酸受体(FRs)。通过荧光图像和 SERS 图谱的竞争实验,验证了内吞作用机制。此外,与没有二氧化硅壳的 GNRs 相比,探针的细胞毒性通过 MTT 试验得到了显著降低。与传统的成像探针相比,这种新型纳米探针在活细胞的多重成像中具有巨大的潜力,这可以通过荧光和 SERS 信号很容易地实现。