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Time-resolved enzymatic determination of glucose using a fluorescent europium probe for hydrogen peroxide
Authors:Meng?Wu,Zhihong?Lin,Axel?Dürkop,Otto?S.?Wolfbeis  author-information"  >  author-information__contact u-icon-before"  >  mailto:Otto.Wolfbeis@chemie.uni-regensburg.de"   title="  Otto.Wolfbeis@chemie.uni-regensburg.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, 93040 Regensburg, Germany
Abstract:An enzymatic assay for glucose based on the use of the fluorescent probe for hydrogen peroxide, europium(III) tetracycline (EuTc), is described. The weakly fluorescent EuTc and enzymatically generated H2O2 form a strongly fluorescent complex (EuTc–H2O2) whose fluorescence decay profile is significantly different. Since the decay time of EuTc–H2O2 is in the microseconds time domain, fluorescence can be detected in the time-resolved mode, thus enabling substantial reduction of background fluorescence. The scheme represents the first H2O2-based time-resolved fluorescence assay for glucose not requiring the presence of a peroxidase. The time-resolved assay (with a delay time of 60 mgrs and using endpoint detection) enables glucose to be determined at levels as low as 2.2 mgrmol L–1, with a dynamic range of 2.2–100 mgrmol L–1. The method also was adapted to a kinetic assay in order to cover higher glucose levels (mmol L–1 range). The latter was validated by analyzing spiked serum samples and gave a good linear relationship for glucose levels from 2.5 to 55.5 mmol L–1. Noteworthy features of the assay include easy accessibility of the probe, large Stokesrsquo shift, a line-like fluorescence peaking at 616 nm, stability towards oxygen, a working pH of approximately 7, and its suitability for both kinetic and endpoint determination.
Keywords:Glucose  Europium  Fluorescent probe  Hydrogen peroxide  Time-resolved fluorescence
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