Abstract

Up-conversion nanoparticles (UCNPs), especially single-band bright red UCNPs, have better penetration of biological tissues, absorb less lost energy, and have higher sensitivity and accuracy in the determination of actual biological samples in the field of biosensing. Here, a novel colorimetric and fluorescent dual-channel method based upon an internal filtration effect (IFE) quenching mechanism was proposed for the quantitative analysis of xanthine (XA) by using red UCNPs as fluorescence indicator and 3,3′,5,5′ -tetramethylbenzidine (TMB) as chromogenic substrate. The sensitivity of the detection system was also enhanced by a cycle signal amplification strategy based on the Fenton reaction. Under the best conditions, the detection limits of XA by fluorescent and colorimetric methods were 0.58 μM and 1.19 μM, respectively. The developed method was applied to the detection of XA in actual serum samples, and the recoveries of the spiked samples by fluorescent and colorimetric methods were in the range of 96.3–104.3 % and 94.3–105.4 %, respectively. In addition, the commercial ELISA method was used to verify the application of the proposed method and the test results of XA were close to those obtained by fluorescent and colorimetric methods, indicating that the accuracy of the developed nanosensing system was acceptable.

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