Chen Zhengbo, Tan Lulu, Hu Liangyu, Zhang Yimeng, Wang Shaoxiong, Lv Fanyi
Department of Chemistry, Capital Normal University , Beijing 100048, China.
ACS Appl Mater Interfaces. 2016 Jan 13;8(1):102-8. doi: 10.1021/acsami.5b08975. Epub 2015 Dec 31.
We presented a simple, cost-effective, and ultrasensitive colorimetric approach for visually detecting thrombin by the catalytic amplification of gold nanoparticles (AuNPs) and aptamer-thrombin recognition. Thrombin can be quantified in the presence of catalytic AuNP surface by using color-change time of 4-nitrophenol. Without thrombin, yellow 4-nitrophenol can freely access the surface of AuNP and becomes colorless 4-aminophenol. With the addition of thrombin, aptamer-thrombin with large size interaction masks the partial surfaces of AuNPs, and increases the reduction time of 4-nitrophenol to 4-aminophenol. The maximum number of bound thrombin fully mask the catalytic AuNP surface, and thus 4-nitrophenol cannot approach to AuNP surface, the color of the solution remains yellow. The limit of detection (LOD) of 0.1 nM can be achieved with naked eyes. Of note, the method was further applied for the detection of thrombin in human serum samples, showing the results in agreement with those values obtained in an immobilization buffer by the colorimetric method.
我们提出了一种简单、经济高效且超灵敏的比色法,通过金纳米颗粒(AuNPs)的催化放大和适配体 - 凝血酶识别来视觉检测凝血酶。在催化性AuNP表面存在的情况下,可利用4 - 硝基苯酚的颜色变化时间对凝血酶进行定量。没有凝血酶时,黄色的4 - 硝基苯酚可自由进入AuNP表面并变成无色的4 - 氨基苯酚。加入凝血酶后,具有大尺寸相互作用的适配体 - 凝血酶会掩盖AuNPs的部分表面,并增加4 - 硝基苯酚还原为4 - 氨基苯酚的时间。结合的凝血酶数量达到最大值时会完全掩盖催化性AuNP表面,因此4 - 硝基苯酚无法接近AuNP表面,溶液颜色保持黄色。肉眼可实现的检测限(LOD)为0.1 nM。值得注意的是,该方法进一步应用于检测人血清样品中的凝血酶,结果与通过比色法在固定缓冲液中获得的值一致。