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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >A fluorescence detection of D-penicillamine based on Cu2+-induced fluorescence quenching system of protein-stabilized gold nanoclusters
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A fluorescence detection of D-penicillamine based on Cu2+-induced fluorescence quenching system of protein-stabilized gold nanoclusters

机译:基于铜离子诱导的蛋白质稳定金纳米团簇的荧光猝灭系统荧光检测D-青霉胺

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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.
机译:在这一贡献中,由牛血清白蛋白合成的发光金纳米簇作为新型荧光探针被成功地首次用于D-青霉胺的测定。铜离子用于淬灭金纳米团簇的强荧光,而D-青霉胺的添加导致Cu2 +-金纳米团簇体系的荧光强度明显恢复。在最佳条件下,D-青霉胺引起的Cu2 +-金纳米簇系统的荧光强度增加与D-青霉胺的浓度在2.0 x 10(-5)-2.39 x 10(-4)M范围内成线性比例关系D-青霉胺的检出限为5.4 x 10(-6)M.随着650 nm的荧光信号接近近红外区域,本D-青霉胺检测传感器灵敏度高,光谱干扰小。 。此外,基于金纳米团簇的新型荧光传感器已用于测定实际生物样品中的D-青霉胺,结果令人满意。 (C)2014 Elsevier B.V.保留所有权利。

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