An improved method for ratiometric fluorescence detection of pH and Cd2+ using fluorescein isothiocyanate-quantum dots conjugates

被引:97
作者
Gui, Rijun [1 ,2 ]
An, Xueqin [1 ]
Huang, Wenxue [1 ]
机构
[1] E China Univ Sci & Technol, Sch Chem & Mol Engn, Dept Phys Chem, Shanghai 200237, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Dept Chem, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Quantum dots; Fluorescein isothiocyanate; Ratiometric sensor; Fluorescence; SENSOR; CDTE; CDSE; CADMIUM; PROBES; PHOTOLUMINESCENCE; NANOCRYSTALS; BIOSENSORS; GREEN;
D O I
10.1016/j.aca.2013.01.006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, thioglycolic acid capped-CdTe quantum dots (QDs) were modified by polyethylenimine (PEI), and then combined with fluorescein isothiocyanate (FITC) to fabricate FITC-CdTe conjugates. The self-assembly of FITC, CdTe and PEI was ascribed to electrostatic interactions in aqueous solution. The resulting conjugates were developed toward two routes. In route one, ratiometric photoluminescence (PL) intensity of conjugates (I-FITC/I-QDs) was almost linear toward pH from 5.3 to 8.7, and a ratiometric PL sensor of pH was favorable obtained. In route two, firstly added S2- induced remarkable quenching of QDs PL peak (at the "OFF" state), which was restored due to following addition of Cd2+ (at the "ON" state). In the conjugates, successive introduction of S2- and Cd2+ hardly influenced on FITC PL peaks. According to this PL "OFF-ON" mode, a ratiometric PL method for the detection of Cd2+ was achieved. Experimental results confirmed that the I-FITC/I-QDs exhibited near linear proportion toward Cd2+ concentration in the range from 0.1 to 15 mu M, and the limit of detection was 12 nM. Interferential experiments adequately testified that the proposed sensors of pH and Cd2+ were practicable in real samples and complex systems. In comparison with conventional analytical techniques, the ratiometric PL method was simple, rapid, economic and highly selective. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:134 / 140
页数:7
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