State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China; University of Chinese Academy of Sciences, Beijing, 100039, China; Department of Chemistry and Environmental Engineering, Changchun University of Science and Technology, Changchun, China.
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China; University of Chinese Academy of Sciences, Beijing, 100039, China.
Biosens Bioelectron. 2015 Nov 15;73:1-6. doi: 10.1016/j.bios.2015.05.044. Epub 2015 May 22.
Simple, rapid, sensitive and specific detection of cancer cells is of great importance for early and accurate cancer diagnostics and therapy. By coupling nanotechnology and dual-aptamer target binding strategies, we developed a colorimetric assay for visually detecting cancer cells with high sensitivity and specificity. The nanotechnology including high catalytic activity of PtAuNP and magnetic separation & concentration plays a vital role on the signal amplification and improvement of detection sensitivity. The color change caused by small amount of target cancer cells (10 cells/mL) can be clearly distinguished by naked eyes. The dual-aptamer target binding strategy guarantees the detection specificity that large amount of non-cancer cells and different cancer cells (10(4) cells/mL) cannot cause obvious color change. A detection limit as low as 10 cells/mL with detection linear range from 10 to 10(5) cells/mL was reached according to the experimental detections in phosphate buffer solution as well as serum sample. The developed enzyme-free and cost effective colorimetric assay is simple and no need of instrument while still provides excellent sensitivity, specificity and repeatability, having potential application on point-of-care cancer diagnosis.
简单、快速、灵敏和特异的癌细胞检测对于癌症的早期准确诊断和治疗至关重要。通过结合纳米技术和双适体靶标结合策略,我们开发了一种比色分析方法,可高灵敏度和高特异性地可视化检测癌细胞。包括 PtAuNP 的高催化活性在内的纳米技术以及磁分离和浓缩在信号放大和提高检测灵敏度方面发挥了重要作用。少量靶标癌细胞(10 个细胞/mL)引起的颜色变化可以通过肉眼清楚地区分。双适体靶标结合策略保证了检测的特异性,大量非癌细胞和不同癌细胞(10(4)个细胞/mL)不会引起明显的颜色变化。根据在磷酸盐缓冲溶液和血清样本中的实验检测,该方法的检测限低至 10 个细胞/mL,检测线性范围为 10 到 10(5)个细胞/mL。开发的无酶且经济有效的比色分析方法简单,无需仪器,同时仍具有出色的灵敏度、特异性和可重复性,在即时癌症诊断方面具有潜在的应用价值。