“…Thus far, a number of analytical methods in the literature have been reported for the analysis of NT-proBNP, including radioimmunoassay (RIA) [ 11 ], colorimetry [ 12 ], fluorescent bead-based immunoassay [ 13 ], chemiluminescent immunoassay [ 14 ], dynamic light scattering [ 15 , 16 ], surface-enhanced Raman scattering [ 17 ], amperometric immunosensors based on enzyme label [ 18 ], silver nanoparticle label method [ 19 ], silver nanodisk label method [ 20 ], photoelectrochemical immunosensor method [ 21 ], electrochemiluminescent (ECL) immunosensor method [ 22 ], field-effect transistor biosensor method [ 23 ], giant magnetoresistance assay [ 24 ], and fluorescence-based lateral flow immunoassay [ 25 ]. While very sensitive electrochemical biosensors for the detection of NT-proBNP have been reported [ 18 , 19 , 20 , 21 , 22 , 23 ], the requirement of a reference electrode in electrochemical biosensors may be a weak point, as liquid junction error often exists in practical situations [ 26 ]. Optical sensors do not require a so-called reference optrode, and also have the advantages of immunity to electromagnetic interference.…”