Electrochemiluminescence
(ECL)-functionalized metal–organic
frameworks (MOFs) have attracted increasing attention in biosensing
in virtue of their diverse and tunable optical properties. A famous
ECL luminophore, carboxyl-rich tris(4,4′-dicarboxylic acid-2,2′-bipyridyl)
ruthenium(II) (Ru(dcbpy)3
2+), possesses the
characteristics of good water solubility and excellent ECL performance
and also has the potential to be the organic ligand of metal–organic
frameworks. Herein, functionalized MOF nanosheets (RuMOFNSs) containing
plenty of Ru(dcbpy)3
2+ in the frameworks were
synthesized in aqueous solution by a simple one-pot method. In this
protocol, Ru(dcbpy)3
2+ acted as organic ligand
to coordinate with Zn2+ originated from Zn(NO3)2, and polyvinylpyrrolidone (PVP) was used as structure-directing
agent to control the formation of sheetlike structure. For practical
application, a “signal-on” ECL immunosensor was designed
for cardiac troponin I (cTnI) detection by employing RuMOFNSs as ECL
probe. The immunosensor exhibited high sensitivity and excellent selectivity
for cTnI detection in the range from 1 fg/mL to 10 ng/mL with a detection
limit as low as 0.48 fg/mL. Finally, the biosensor was successfully
applied for the detection of cTnI in human serum sample with satisfactory
results, demonstrating its potential application in bioanalysis and
clinical diagnosis.
Ratiometric electrochemiluminescence (ECL) has attracted special focus in the biological analysis field, because it could eliminate the environmental interference and allow for precise measurement. Herein, a dual-wavelength ratiometric ECL biosensor was designed for the detection of cardiac troponin I (cTnI), where (4,4′-dicarboxylic acid-2,2′bipyridyl) ruthenium(II) (Ru(dcbpy) 3 2+ ) and Au nanoparticle-loaded graphene oxide/polyethylenimine (GPRu− Au) nanomaterial acts as an acceptor, and Au nanoparticlemodified graphitic phase carbon nitride nanosheet composite (Au−CNN) acts as donor. Au−CNN shows a high and steady ECL signal centered at 455 nm, which is well-matched with the adsorption of GPRu−Au; thereby, a highly efficient electrochemiluminescent resonance energy transfer (ECL-RET) sensing platform is designed. AuNPs facilitate the immobilization of antibody on the nanomaterials through a Au−N bond. The high surface area of graphene oxide/polyethylenimine allows a large number of Ru(dcbpy) 3 2+ to be loaded, immensely amplifying the ECL signal. This sensing platform exhibits outstanding analytical performance toward cTnI with a detection limit of 3.94 fg/mL (S/N = 3). The high reliability, selectivity, and sensitivity of this ratiometric ECL biosensor provides a versatile sensing platform for the bioanalysis.
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