Abstract
In this work, we report an ultrasensitive colorimetric sensing strategy for Cu2+ based on the Cu2+ catalyzed TMB-H2O2 reaction, and the signal amplification induced by aptamer-K+-Cu2+ complex. It is demonstrated that Cu2+ exhibits an intrinsic peroxidase-like catalytic activity. Thus, we utilize the catalytic activity of Cu2+ to TMB-H2O2 reaction for direct colorimetric visualization of Cu2+ for the first time. The limit of detection (LOD) is 2.6μM. To further improve the sensitivity of Cu2+ detection, we utilized G-quadruplex-Cu2+ metalloenzyme complex formed by K+, G-rich DNA, and Cu2+ to amplify colorimetric signal of TMB-H2O2 reaction. The LOD is as low as 0.076μM, which is 34-fold lower than that of only Cu2+-catalyzed TMB-H2O2 system (2.6μM). The LOD shows excellent potential for monitoring ultralow levels of Cu2+ in water samples.
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