Wang Yu Winston, Kang Soyoung, Khan Altaz, Bao Philip Q, Liu Jonathan T C
Department of Mechanical Engineering, University of Washington, Seattle, WA 98195, USA.
Department of Biomedical Engineering, Stony Brook University (SUNY), Stony Brook, NY 11794, USA.
Biomed Opt Express. 2015 Sep 1;6(10):3714-23. doi: 10.1364/BOE.6.003714. eCollection 2015 Oct 1.
The biological investigation and detection of esophageal cancers could be facilitated with an endoscopic technology to screen for the molecular changes that precede and accompany the onset of cancer. Surface-enhanced Raman scattering (SERS) nanoparticles (NPs) have the potential to improve cancer detection and investigation through the sensitive and multiplexed detection of cell-surface biomarkers. Here, we demonstrate that the topical application and endoscopic imaging of a multiplexed cocktail of receptor-targeted SERS NPs enables the rapid detection of tumors in an orthotopic rat model of esophageal cancer. Antibody-conjugated SERS NPs were topically applied on the lumenal surface of the rat esophagus to target EGFR and HER2, and a miniature spectral endoscope featuring rotational scanning and axial pull-back was employed to comprehensively image the NPs bound on the lumen of the esophagus. Ratiometric analyses of specific vs. nonspecific binding enabled the visualization of tumor locations and the quantification of biomarker expression in agreement with immunohistochemistry and flow cytometry validation data.
利用内镜技术筛查癌症发生之前及伴随过程中的分子变化,有助于对食管癌进行生物学研究和检测。表面增强拉曼散射(SERS)纳米颗粒(NPs)有潜力通过对细胞表面生物标志物进行灵敏且多重的检测,来改善癌症检测和研究。在此,我们证明,对受体靶向SERS NPs的多重混合物进行局部应用和内镜成像,能够在原位大鼠食管癌模型中快速检测肿瘤。将抗体偶联的SERS NPs局部应用于大鼠食管腔表面,以靶向表皮生长因子受体(EGFR)和人表皮生长因子受体2(HER2),并采用具有旋转扫描和轴向回拉功能的微型光谱内镜,对结合在食管腔内的NPs进行全面成像。通过对特异性结合与非特异性结合进行比率分析,能够实现肿瘤位置的可视化,并对生物标志物表达进行定量,这与免疫组织化学和流式细胞术验证数据一致。