Novel Electrochemiluminescence-Sensing Platform for the Precise Analysis of Multiple Latent Tuberculosis Infection Markers.

Latent tuberculosis infection (LTBI) is one of the major contributing factors for the high incidence of tuberculosis, and the low contents of LTBI markers in human serum present a great challenge for the diagnosis of LTBI. Here, we reported a novel electrochemiluminescence (ECL)-sensing platform for the precise analysis of multiple LTBI markers, interferon-gamma (IFN-γ) and interleukin (IL)-2. In this approach, self-prepared carbon quantum dots (CQDs) and luminol were integrated onto gold nanoparticles (AuNPs), which were further enriched on the surface of magnetic bead (MB) to create two solid-phase ECL nanoprobes (MB@Au@CQDs and MB@Au@luminol) for improving the detection sensitivity efficiently. Graphene oxide (GO) and AuNPs were electrodeposited onto a patterned indium tin oxide (ITO) electrode with two spatially resolved areas in sequence to form two sensitive and stable sensing areas. IFN-γ-antibody (Ab)1 and IL-2-Ab1 were separately immobilized on the two sensing areas to capture the corresponding LTBI markers, which were further recognized by IFN-γ-Ab2 and IL-2-Ab2 labeled as MB@Au@CQDs and MB@Au@luminol. The ECL intensity depended linearly on the content of IFN-γ and IL-2 in the range of 0.01-1000 pg mL-1, with a low detection limit of 10 fg mL-1. The proposed ECL-sensing platform is simple, sensitive, accurate, reliable, and specific to the detection of rare IFN-γ and IL-2 in human serum and provides a valuable protocol for facilitating fast and precise diagnosis of LTBI.

Graphene oxide amplified electrochemiluminescence of graphitic carbon nitride and its application in ultrasensitive sensing for Cu(2+).

Here for the first time, we present a novel electrochemiluminescence (ECL) sensor based on graphitic carbon nitride/graphene oxide (g-C3N4/GO) hybrid for the ultrasensitive detection of Cu(2+), which is a common pollutant in environmental system. The g-C3N4/GO shows stable ECL signal in the presence of the self-produced coreactant from oxygen reduction, and the ECL signal could be effectively quenched by Cu(2+), the possible ECL detection mechanism has been proposed in detail. GO can not only significantly enhance the cathodic ECL signal of g-C3N4 (∼3.8 times), but also serve as immobilization platform for g-C3N4. After optimization of experimental conditions, the proposed protocol can offer an ultrasensitive, highly selective and recyclable method for the detection of Cu(2+) with a low detection limit of 1.0 × 10(-11) M and a wide linear range from 1.0 × 10(-11) to 1.0 × 10(-7) M. Moreover, the practicability of the ECL sensor in real wastewater samples is also tested, showing that the proposed ECL sensor could be a promising alternative method for the emergency and routine monitoring of Cu(2+) in real sample.