Qian Ximei, Peng Xiang-Hong, Ansari Dominic O, Yin-Goen Qiqin, Chen Georgia Z, Shin Dong M, Yang Lily, Young Andrew N, Wang May D, Nie Shuming
Departments of Biomedical Engineering and Chemistry, Emory University and Georgia Institute of Technology, 101 Woodruff Circle, Suite 2001, Atlanta, Georgia 30322, USA.
Nat Biotechnol. 2008 Jan;26(1):83-90. doi: 10.1038/nbt1377. Epub 2007 Dec 23.
We describe biocompatible and nontoxic nanoparticles for in vivo tumor targeting and detection based on pegylated gold nanoparticles and surface-enhanced Raman scattering (SERS). Colloidal gold has been safely used to treat rheumatoid arthritis for 50 years, and has recently been found to amplify the efficiency of Raman scattering by 14-15 orders of magnitude. Here we show that large optical enhancements can be achieved under in vivo conditions for tumor detection in live animals. An important finding is that small-molecule Raman reporters such as organic dyes were not displaced but were stabilized by thiol-modified polyethylene glycols. These pegylated SERS nanoparticles were considerably brighter than semiconductor quantum dots with light emission in the near-infrared window. When conjugated to tumor-targeting ligands such as single-chain variable fragment (ScFv) antibodies, the conjugated nanoparticles were able to target tumor biomarkers such as epidermal growth factor receptors on human cancer cells and in xenograft tumor models.
我们描述了基于聚乙二醇化金纳米颗粒和表面增强拉曼散射(SERS)的用于体内肿瘤靶向和检测的生物相容性且无毒的纳米颗粒。胶体金已被安全地用于治疗类风湿性关节炎50年,并且最近发现它能将拉曼散射效率提高14 - 15个数量级。在此我们表明,在体内条件下可实现用于活体动物肿瘤检测的大光学增强。一个重要发现是,诸如有机染料等小分子拉曼报告分子未被取代,而是通过硫醇修饰的聚乙二醇得以稳定。这些聚乙二醇化的SERS纳米颗粒比在近红外窗口发光的半导体量子点亮得多。当与肿瘤靶向配体如单链可变片段(ScFv)抗体偶联时,偶联的纳米颗粒能够靶向肿瘤生物标志物,如人癌细胞和异种移植肿瘤模型中的表皮生长因子受体。