ABSTRACT
Acetaminophen is one of the most commonly used non-steroidal anti-inflammatory drugs worldwide. However, due to the increasing popularity of this drug, overdosing and the contamination of ambient waterways have emerged as major issues. Here, we report on a reliable, ultrasensitive, and easy-to-use sensor for the electrochemical detection of acetaminophen. This sensor employs a gold wire electrode with a unique three-dimensional hierachical nanoporous structure, fabricated using a dissolution, disproportion and deposition procedure. In consideration of optimal sensitivity and reproducibility, the most suitable nanoporous gold electrode was employed for the detection of acetamiophen among a set of nanoporous electrodes made under different reaction times. It was found that the pore size, film thickness, and electrochemically active surface area (ECSA) played major roles in the fouling resistance of the developed sensor. The ECSA of the selected sensor was increased by 15.8 times after the post-treatment. The 3D nanoporous electrode demonstrated excellent performance for the detection of acetaminophen with a low detection limit of 3.37 nM, and a strong anti-interference capability. The developed nanoporous Au electrode proved effective for the detection of acetaminophen in real sheep serum, which confirmed its promising application for medical diagnostics and pollutant surveilliance in source waters.
Subject(s)
Gold , Nanopores , Acetaminophen , Animals , Electrochemical Techniques , Electrodes , Reproducibility of Results , SheepABSTRACT
Here we report on a selective and sensitive graphene-oxide-based electrochemical sensor for the detection of naproxen. The effects of doping and oxygen content of various graphene oxide (GO)-based nanomaterials on their respective electrochemical behaviors were investigated and rationalized. The synthesized GO and GO-based nanomaterials were characterized using a field-emission scanning electron microscope, while the associated amounts of the dopant heteroatoms and oxygen were quantified using x-ray photoelectron spectroscopy. The electrochemical behaviors of the GO, fluorine-doped graphene oxide (F-GO), boron-doped partially reduced graphene oxide (B-rGO), nitrogen-doped partially reduced graphene oxide (N-rGO), and thermally reduced graphene oxide (TrGO) were studied and compared via cyclic voltammetry (CV) and differential pulse voltammetry (DPV). It was found that GO exhibited the highest signal for the electrochemical detection of naproxen when compared with the other GO-based nanomaterials explored in the present study. This was primarily due to the presence of the additional oxygen content in the GO, which facilitated the catalytic oxidation of naproxen. The GO-based electrochemical sensor exhibited a wide linear range (10 mM-1 mM), a high sensitivity (0.60 µAµM-1cm-2), high selectivity and a strong anti-interference capacity over potential interfering species that may exist in a biological system for the detection of naproxen. In addition, the proposed GO-based electrochemical sensor was tested using actual pharmaceutical naproxen tablets without pretreatments, further demonstrating excellent sensitivity and selectivity. Moreover, this study provided insights into the participatory catalytic roles of the oxygen functional groups of the GO-based nanomaterials toward the electrochemical oxidation and sensing of naproxen.
