Abstract
Colorimetry can identify the detection results visually by a naked eye, but the disadvantages such as low sensitivity and high background signal seriously limit its application prospects. In this paper, we prepared Fe@Co-N stellate porous carbon nanoenzyme with a large specific surface area containing Fe-N and cobalt double peroxide active sites. A dual catalytic system of the nanoenzyme and G-quadruplex/Hemin DNAzyme was constructed, which maintained independent catalytic spaces. And a colorimetric biosensor with a low background signal and ultra-sensitive detection of tetracyclines based on a shared structure was developed. Tetracyclines could adsorb hemin from nearby G-quadruplexes to form multimers that were detached from the system by cyclic shearing of exonuclease I, achieving highly sensitive detection of low concentrations of antibiotics. The limit of detection (LOD) of 0.333 ng/mL (S/N = 3) was much lower than those of most detection methods, indicating the promising strategy could be applied for the simultaneous detection of multiple tetracyclines.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.