The evaluation of pyrophosphatase (PPase) activity plays an important role in diagnosing diseases and understanding the function of PPase in the related biological events. In this work, an inhibition effect of pyrophosphate (PPi) on Cu(2+)-catalyzed H2O2-mediated oxidation of 2,2-azinobis(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) was observed. We utilize this inhibition effect to develop a convenient label free visual method for PPase activity detection. A hydroxyl radical could be generated from a Cu(2+)-based Fenton-like reaction, and then reacted with ABTS to produce colored ABTS˙(+). The strong complexation between PPi and Cu(2+) disturbed this Cu(2+)-catalyzed ABTS-H2O2 reaction probably due to changing redox potentials of Cu(2+) towards H2O2. The PPase-catalyzed hydrolysis of PPi into Pi prohibited the complexation, resulting in the recovery of catalytic capability of Cu(2+). As a result, the solution color changed from colorless to green with a remarkable increase of absorbance. Compared with the traditional PPase assays, the developed visual assay is cost-effective and easy to implement. And a high sensitivity for PPase with a detection limit of 0.027 U mL(-1) was achieved. Moreover, the proposed colorimetric strategy was also applied to evaluate PPase inhibition and exhibited a good assay performance in complex biological samples.

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We have developed a microchip electrophoresis (MCE)-based fluorescence signal amplification strategy as a universal MCE method for the detection of trace biomolecules. This strategy exhibits high sensitivity and specificity for target molecules, and has been applied for the detection of interferon-gamma (IFN-γ) in human plasma with satisfactory results.

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