Wu Meng, Lin Zhihong, Dürkop Axel, Wolfbeis Otto S
Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg, 93040 Regensburg, Germany.
Anal Bioanal Chem. 2004 Oct;380(4):619-26. doi: 10.1007/s00216-004-2785-9. Epub 2004 Oct 6.
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 micros and using endpoint detection) enables glucose to be determined at levels as low as 2.2 micromol L(-1), with a dynamic range of 2.2-100 micromol 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 Stokes' 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.
本文描述了一种基于使用过氧化氢荧光探针铕(III)四环素(EuTc)的葡萄糖酶法测定方法。弱荧光的EuTc与酶促产生的H2O2形成强荧光复合物(EuTc-H2O2),其荧光衰减曲线明显不同。由于EuTc-H2O2的衰减时间在微秒时域内,因此可以在时间分辨模式下检测荧光,从而大幅降低背景荧光。该方案代表了第一种基于H2O2的无需过氧化物酶存在的葡萄糖时间分辨荧光测定法。时间分辨测定法(延迟时间为60微秒并使用终点检测)能够测定低至2.2微摩尔/升的葡萄糖水平,动态范围为2.2-100微摩尔/升。该方法还适用于动力学测定以覆盖更高的葡萄糖水平(毫摩尔/升范围)。通过分析加标血清样本对后者进行了验证,结果表明葡萄糖水平在2.5至55.5毫摩尔/升范围内具有良好的线性关系。该测定法的显著特点包括探针易于获取、斯托克斯位移大、在616纳米处有类似线状的荧光峰值、对氧气稳定、工作pH约为7,以及适用于动力学和终点测定。