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It is of great significance to sense clioquinol (CQ) in a simple and fast way because of its potential application in the treatment of neurodegenerative diseases. In this contribution, we proposed a Cu2+-mediated fluorescence switchable strategy to detect CQ by taking bovine serum albumin (BSA) protected gold nanoclusters (AuNCs) as probes. It was found that the strong red fluorescence of BSA-protected AuNCs at 610 nm could be effectively quenched by Cu2+ (off state) and reversibly recovered by CQ (on state) owing to the specific coordination of CQ and Cu2+. Under the optimal conditions, there was a good linear relationship between the off–on efficiency (Eoff–on) and the amount of CQ in the range of 1–12 μM (R2 = 0.9902), with a detection limit of 0.63 μM (3σ). The “turn off–on” mode and the fast and unique complexation of CQ and Cu2+ endow AuNCs with high specificity for CQ sensing. The proposed strategy is label-free, fast and selective, which is applicable to the analysis of CQ in cream with satisfactory results.

Graphical abstract: Cu2+-mediated fluorescence switching of gold nanoclusters for the selective detection of clioquinol

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