In this work, based on electrochemiluminescence (ECL) technology and self-assembled portable disease detection chips, a bioactivity-maintained sensing platform was developed for the quantitative detection of neuron-specific enolase. First, we prepared FeO@MoS nanocomposites as an efficient catalyst to accelerate the reduction of persulfate (SO). Specifically, abundant sulfate radicals (SO) were generated because of cyclic conversion between Fe and Fe. Meanwhile, MoS nanoflowers with a high specific surface area could not only load more FeO but also solve its agglomeration problem, which greatly improved the catalytic efficiency. Moreover, a biosensor chip was constructed by standard lithography processes for disease detection, which had good sensitivity and portability. According to the above strategies, the developed portable sensing platform played the part of promoting the practical application of bioanalysis in early tumor screening and clinical diagnosis. In addition, we developed a short peptide ligand (NARKFYKG, NAR) to avoid the occupation of antigen binding sites by specifically connecting to Fc fragments in antibodies. Thus, the binding efficiency of antibodies and the activity of biosensors were improved due to the introduction of NAR.
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http://dx.doi.org/10.1021/acs.analchem.2c01868 | DOI Listing |
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