A fluorescence detection of D-penicillamine based on Cu2+-induced fluorescence quenching system of protein-stabilized gold nanoclusters

被引:34
作者
Wang, Peng [1 ]
Li, Bang Lin [1 ]
Li, Nian Bing [1 ]
Luo, Hong Qun [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Key Lab Luminescent & Real Time Analyt Chem, Minist Educ, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
D-Penicillamine; Fluorescence; Gold nanoclusters; Cupric ion; Turn-on sensor; AU NANOCLUSTERS; DOSAGE FORMS; ELECTROCATALYTIC OXIDATION; SELECTIVE DETERMINATION; SENSITIVE DETECTION; QUANTUM DOTS; ELECTRODE; SENSOR; DERIVATIZATION; FLUORESCAMINE;
D O I
10.1016/j.saa.2014.06.082
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
In this contribution, a luminescent gold nanoclusters which were synthesized by bovine serum albumin as novel fluorescent probes were successfully utilized for the determination of D-penicillamine for the first time. Cupric ion was employed to quench the strong fluorescence of the gold nanoclusters, whereas the addition of D-penicillamine caused obvious restoration of fluorescence intensity of the Cu2+-gold nanoclusters system. Under optimum conditions, the increment in fluorescence intensity of Cu2+-gold nanoclusters system caused by D-penicillamine was linearly proportional to the concentration of D-penicillamine in the range of 2.0 x 10(-5)-2.39 x 10(-4) M. The detection limit for D-penicillamine was 5.4 x 10(-6) M. With the off-on fluorescence signal at 650 nm approaching the near-infrared region, the present sensor for D-penicillamine detection had high sensitivity and low spectral interference. Furthermore, the novel gold nanoclusters-based fluorescent sensor has been applied to the determination of D-penicillamine in real biological samples with satisfactory results. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:198 / 202
页数:5
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