Abstract
Herein, a spectrum-resolved differential strategy was proposed to enhance further the selectivity of photoelectrochemical (PEC) sensors, demonstrated by the simultaneous determinations of ascorbic acid (AA) and uric acid (UA). Molecularly imprinted polymer (MIP) membranes for AA (MIPAA) and UA (MIPUA) were fabricated on the surface of TiO2 nanotubes via electropolymerization, using pyrrole as functional monomer, AA and UA as templates, respectively. It was shown that the increase in absorbance from AA or UA within the MIP membranes resulted in an intense decrease in the photocurrent of the PEC sensors. In the spectrum-resolved differential mode, ΔRIAA= (IAA/IAA0−IUA/IUA0)310 and ΔRIUA= (IUA0/IUA −IAA0/IAA)275 were used in the simultaneous determinations of AA and UA, respectively. Where IAA, IAA0, IUA and IUA0 are the photocurrents of MIPAA and MIPUA in sample and blank, the subscripts of 275 and 310 stand for the excitation wavelength (nm), respectively. The interference levels in the differential mode were reduced by one order of magnitude compared with the normal MIP mode. The spectrum-resolved differential PEC MIP sensors were used in the simultaneous determination of AA and UA in serum and urine samples, with the detection limits of 0.019 and 0.036 μM, respectively.
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