Luo Yawen, Miao Hong, Yang Xiaoming
College of Pharmaceutical Sciences, Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, Southwest University, Chongqing 400715, China.
College of Pharmaceutical Sciences, Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, Southwest University, Chongqing 400715, China.
Talanta. 2015 Nov 1;144:488-95. doi: 10.1016/j.talanta.2015.07.001. Epub 2015 Jul 4.
Glutathione (GSH), playing roles as both a reducing reagent and protecting ligand, has been successfully employed for synthesizing Cu nanoclusters (CuNCs@GSH) on the basis of a simple and facile approach. The as-prepared CuNCs exhibited a fluorescence emission at 600nm with a quantum yield (QY) of approximately 3.6%. Subsequently, the CuNCs described here was employed as a broad-range pH sensor by virtue of the fluorescence intensity of CuNCs responding sensitively to pH fluctuating in a linear range of 4.0-12.0. Meanwhile, these prepared CuNCs were applied for detections of vitamin B1 (VB1) on the basis of positively charged VB1 neutralizing the negative surface charge of CuNCs, thus leading to the instability and aggregations of CuNCs, and further facilitating to quench their fluorescence. In addition, the proposed analytical method permitted detecting VB1 with a linear range of 2.0×10(-8)-1.0×10(-4) mol L(-1) as well as a detection limit of 4.6×10(-9) mol L(-1). Eventually, the practicability of this sensing approach was validated by assaying VB1 in human urine samples and pharmaceutical tablets, confirming its potential to broaden avenues for assaying VB1.
谷胱甘肽(GSH)兼具还原剂和保护配体的作用,已基于一种简单便捷的方法成功用于合成铜纳米簇(CuNCs@GSH)。所制备的CuNCs在600nm处呈现荧光发射,量子产率(QY)约为3.6%。随后,鉴于CuNCs的荧光强度对4.0 - 12.0线性范围内的pH波动敏感响应,此处描述的CuNCs被用作宽范围pH传感器。同时,这些制备的CuNCs基于带正电荷的维生素B1(VB1)中和CuNCs的负表面电荷,从而导致CuNCs的不稳定性和聚集,并进一步促使其荧光猝灭,被应用于VB1的检测。此外,所提出的分析方法能够检测线性范围为2.0×10(-8)-1.0×10(-4) mol L(-1)的VB1,检测限为4.6×10(-9) mol L(-1)。最终,通过检测人尿液样本和药片中的VB1验证了这种传感方法的实用性,证实了其拓宽VB1检测途径的潜力。