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Enzyme-controllable just-in-time production system of copper hexacyanoferrate nanoparticles with oxidase-mimicking activity for highly sensitive colorimetric immunoassay
Nanozymes are a series of elaborately designed nanomaterials that can mimic the catalytic sites of natural enzymes for reactions. Bypassing the tedious design and preparation of nanomaterial, in this work, we report on a novel just-in-time production system of copper hexacyanoferrate nanoparticles (...
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Published in: | Talanta (Oxford) 2022-09, Vol.247, p.123546-123546, Article 123546 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Nanozymes are a series of elaborately designed nanomaterials that can mimic the catalytic sites of natural enzymes for reactions. Bypassing the tedious design and preparation of nanomaterial, in this work, we report on a novel just-in-time production system of copper hexacyanoferrate nanoparticles (CHNPs), which act as an oxidase-mimicking nanozyme. This system can rapidly produce CHNPs nanozyme on demand by simply mixing Cu(II) with potassium hexacyanoferrate(III) (K3[Fe(CN)6]). It is found that once K3[Fe(CN)6] is reduced to K4[Fe(CN)6], the formation of CHNPs is inhibited. Therefore, the just-in-time production system of CHNPs was coupled with alkaline phosphatase (ALP) to construct an enzyme-controllable just-in-time production (ECJP) system, in which ALP could inhibit the production of by catalyzing the hydrolysis of ascorbic acid 2-phosphate (AAP) to generating ascorbic acid (AA). The ECJP system is then used to probe the activity of ALP by employing 2,2′-azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) as the chromogenic substrate, and a detection limit of 0.003 U L−1 was achieved. Moreover, by adapting ALP as the enzyme label, an ECJP system-based colorimetric immunoassay protocol was established for sensitive detection of aflatoxin B1 (AFB1), and a detection limit as low as 0.73 pg mL−1 was achieved. The developed immunoassay method is successfully applied to the detection of AFB1 in peanut samples. The operation of ECJP system is quite simple and the coupling of ALP with CHNPs nanozyme can arouse dual enzyme-like cascade signal amplification. So, we believe this work can offer a new perspective for the development of nanozymes-based biodetection methods and colorimetric immunoassay strategies.
Schematic illustration of (A) template-free just-in-time producing copper hexacyanoferrate(III) strategy as oxidase mimic-based on colorimetric platform, (B) enzyme-controllable manner-based on colorimetric platform, and (C) CHNPs-ABTS-based colorimetric immunoassay. [Display omitted]
•Cu2+ can react rapidly with K3[Fe(CN)6] to yield copper hexacyanoferrate nanoparticles (CHNPs) in situ.•CHNPs can first act as an oxidase-mimicking nanozyme to arise the UV absorbance readout.•The ascorbic acid is used to inhibit the formation of CHNPs by reducing K3[Fe(CN)6].•A signal-on assay mode with the cascade signal amplification is established for aflatoxin B1.•This work provides a practical tool for detection of biomolecules. |
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ISSN: | 0039-9140 1873-3573 |
DOI: | 10.1016/j.talanta.2022.123546 |