Determination Of Acetaminophen Research Articles

Binary and Ternary Deep Eutectic Solvents for Methylene Green Electropolymerization on Multiwalled Carbon Nanotubes: Optimization, Characterization and Application.

Choline chloride (ChCl) based binary and ternary deep eutectic solvents (DES) were evaluated for methylene green electropolymerization with oxalic acid (OA) and ethylene glycol (EG) as hydrogen bond donors. Binary DES ChCl : OA in molar ratios 1 : 1 and 2 : 1 and ChCl : EG 1 : 2 and ternary DES (tDES) in different molar ratios and percentages of water were evaluated. The highest polymer growth was in ChCl : OA : EG-tDES with 13% added water, that had a lower viscosity and higher ionic conductivity when associated with HCl as dopant. This enhanced the formation of more cation radicals and, consequently, more polymer formation. The PMG/MWCNT/GCE-tDES sensor was successfully applied to the simultaneous determination of 5-aminosalicylic acid (5-ASA) and acetaminophen (APAP) by differential pulse voltammetry in the concentration range 1 μM-200 μM, with detection limits of 0.37 μM and 0.49 μM for 5-ASA and APAP, respectively. The sensor demonstrated good repeatability, reproducibility and stability, and was successfully applied in pharmaceutical formulations.

A dual-template molecularly imprinted electrochemical sensor assisted with BO-XGBoost algorithm for simultaneous determination of dopamine and acetaminophen

The simultaneous detection of dopamine (DA) and acetaminophen (AP) is crucial for diagnosing and treating related mental disorders. However, accurately determining DA and AP in biological samples remains challenging due to the interference from other biomolecules, such as ascorbic acid (AA), uric acid (UA), epinephrine (EP), etc. Here, we present a dual-template molecularly imprinted electrochemical sensor for the selective recognition of DA and AP. Reduced graphene(rGO)-gold nanoparticles(AuNPs) composite were utilized to enhance the effective area and increase the electron transfer rate of glassy carbon electrode(GCE), thus the electrochemical response signals were amplified. This sensor combined the advantages of nanocomposites and molecularly imprinted polymer (MIP) to achieve highly sensitive and selective detection of DA and AP. However, decreases in the current response of some analytes and variations in relationships of the peak current versus analyte concentration will occur due to adsorption competition on active sites in multianalyte mixtures, rendering the detection range constrained and traditional linear fitting methods inaccurate for predicting analyte concentrations. Therefore, a concentration prediction model based on XGBoost was developed for the sensor to achieve the reliable multi-component determination of DA and AP within the identical measurement range as individual detection. In this model, nine characteristic parameters were extracted from the differential pulse voltammetry (DPV) response curve and Bayesian optimization (BO) was adopted for automatic hyperparameter search, thereby the prediction errors were reduced and the generalization ability was improved. Experiments indicated that the MIP/AuNPs/rGO/GCE exhibited a wide detection range of 2–240 μM and 3–240 μM for DA and AP, with detection limits down to 0.26 μM and 0.33 μM, respectively. In addition, the intelligent MIP/AuNPs/rGO/GCE sensor based on BO-XGBoost model provides more accurate prediction results for untrained concentration combinations obtained from fetal bovine serum samples, indicating that the proposed detection scheme holds potential in future clinical diagnosis.

High-sensitive electrochemical sensor based on Ni/NiCx-integrated functional carbon nanotubes for simultaneous determination of acetaminophen and dopamine

In complex environmental substance monitoring, the simultaneous detection of single and multiple substances with high sensitivity has been a research focus in the field of electrochemical sensors. Rational selection of appropriate dopants to optimize the electrode material is crucial in this regard. In this work, we employed a multi-doping strategy to effectively enhance the electrocatalytic performance of multi-walled carbon nanotubes (MWCNTs). By doping Ni/NiCx onto MWCNTs, we successfully constructed a heterojunction material (Ni/NiCx-N-MWCNTs). The successful doping of Ni/NiCx allows for the synergistic effects of multiple elements. Ni/NiCx serves as a conductive bridge, forming a three-dimensional network of nanotubes, which effectively reduces the aggregation of carbon nanotubes, exposes more active sites, and enhances electrocatalytic activity. The electrochemical sensor based on Ni/NiCx-N-MWCNTs demonstrated high sensitivity, selectivity, and simultaneous electrochemical detection for acetaminophen (1–150 μM, limit of detection (LOD)=0.56 μM) and dopamine (1–80.0 μM, LOD=0.19 μM). Its excellent reproducibility (relative standard deviation (RSD)=2.01 %) and interference resistance provide Ni/NiCx-N-MWCNTs with significant advantages over other electrode materials, indicating a promising application potential.

Screen-printed carbon electrode modified with AgNPs obtained via green synthesis for acetaminophen determination

Screen-printed carbon electrode modified with AgNPs obtained via green synthesis for acetaminophen determination

MOF derived ZnCo2O4@nitrogen-doped carbon as an electrochemical sensor for simultaneous detection of acetaminophen and p-aminophenol

In this study, a rapid and sensitive electrochemical sensor (ZnCo2O4@NC) based on metal-organic frame (MOF)-derived metal oxide material (ZnCo2O4) and chitosan derived nitrogen-doped carbon material (NC) was successfully constructed for the simultaneous determination of acetaminophen (APAP) and p-aminophenol (PAP). A series of electrochemical experiments proved that the MOF derived ZnCo2O4@NC composite has excellent electrochemical response to APAP and PAP in the phosphate buffer saline (PBS) (pH 7.0). The current response varies linearly with the increase of APAP concentration in the range of 8.0 μmol L−1 to 520 μmol L−1 and PAP concentration in the range of 6.0 μmol L−1 to 420 μmol L−1. The sensitivity and limit of detection (LOD) of ZnCo2O4@NC for APAP and PAP detection are 0.1024 and 0.2749 μA μmol L−1 cm−2, 0.0608 and 0.2489 μmol L−1, respectively. The ZnCo2O4@NC composite modified electrode exhibits good selectivity, reproducibility and stability. Additionally, in the detection for acetaminophen sustained-release tablets, the recovery rates of APAP are in the range of 90.00 % –100.00 %. The theoretical content is consistent with our detection results, showing that this method has good accuracy in actual sample analysis. This study provides an innovative idea to improve electrochemical performance of simultaneous detection of acetaminophen and p-aminophenol through the comprehensive strategy of structural design, heteroatom doping.

Electrochemical sensing for simultaneous determination of dopamine and acetaminophen based on ZIF-8@ZIF-67 derived Co/Mo2C embedded in N-doped carbon hollow nanocages

The exploration of an economical and efficient noble metal-free heterogeneous catalyst is of great significance for the construction of an electrochemical method for the simultaneous detection of Dopamine (DA) and acetaminophen (AC). In this paper, we employed a facile strategy to obtain Co/Mo2C nanoparticles embedded in nitrogen-doped carbon hollow nanocages (Co/Mo2C@N-C HNCs) heterogeneous structure by pyrolyzing ZIF-8@ZIF-67 precursor. The unique hollow structure ensures a fast electron transport channel, N doping regulates the local electronic structure of the catalyst, and the synergistic effect with Mo2C and Co nanoparticles provides more electrocatalytic active sites. The Co/Mo2C@N-C HNCs electrode separates the overlapping voltammetry peaks of DA and AC into two distinct voltammetry peaks (△E=200 mV), thereby selectively determining DA in the presence of AC and vice versa. The transfer coefficient (α) and electron transfer number (n) of DA and AC electrocatalytic oxidation were also studied. Using Co/Mo2C@N-C HNCs as electrode, an electrochemical sensor platform for the simultaneous detection of acetaminophen (AC) and dopamine (DA) was first constructed with linear range of 1–185 μM, and 1–100 μM and low detection limit of 0.35 μM and 0.46 μM for AC and DA, respectively. Satisfactory results have been obtained in the determination of human serum and acetaminophen tablets samples. DFT calculation reveals the molecular mechanisms for DA and AC interacting with the Co/Mo2C@N-C HNCs catalysts. This strategy provides a new idea for the selective determination of several analytes in complex substrates.

Selective Determination of Acetaminophen in Presence of Ascorbic Acid at Poly (p-Methoxyphenol) Electrode

In the present work, we discuss the modification of a gold electrode with p-methoxyphenol and its application as a sensor for acetaminophen (ACP) in a phosphate buffer solution (pH = 7.4). The modified electrode was subsequently employed to determine acetaminophen in the presence of ascorbic acid (AA) using differential pulse voltammetry (DPV). The peak positions and relative sensitivity of ACP/AA were influenced by the potential window used during polymerization. For polymerization between 0 and 1.0 V, the peak potentials recorded in the phosphate buffer solution (pH = 7.4) were 488 mV for ACP and 280 mV vs. Ag/AgCl for AA. Furthermore, the effects of pH and electrolyte type on the linearity range and detection limit were investigated. The high selectivity and sensitivity for ACP were attributed to charge discrimination and analyte accumulation. The detection limit for the 3σ-test was determined to be 0.2 nM. This study highlights the potential of the modified gold electrode for selective and sensitive detection of acetaminophen, even in the presence of interfering substances such as ascorbic acid. The optimization of polymerization conditions and the comprehensive analysis of pH and electrolyte effects contribute to the electrode's superior performance.

Simultaneous voltammetric detection of acetaminophen and levofloxacin based on barley leaves derived carbon decorated with gold nanoparticles

In this study, barley leaves were used as biomass precursor to prepare the ZnCl2 activated barley leaves derived carbon by the carbonization under N2 atmosphere at high temperature (ZnAC). The gold nanoparticles were synthesized in situ on the surface of ZnAC (AuNPs/ZnAC). The as-prepared AuNPs/ZnAC composite was characterized by SEM, Raman spectroscopy, XRD et. al. The AuNPs/ZnAC composite was drop-cast onto the surface of a glassy carbon electrode to fabricate an electrochemical sensing platform for the simultaneous determination of acetaminophen (AC) and levofloxacin (LEV). The results of electrochemical experiments showed that ZnAC and AuNPs had a synergetic electrocatalytic effect on the oxidation of AC and LEV. The oxidation peak potentials of AC and LEV were at 0.57 and 1.02 V, respectively. The proposed sensor allowed the simultaneous quantification of AC and LEV two linear intervals: in the ranges of 0.1–15 and 15–300 μM for AC and 0.1–20 and 20–300 μM for LEV with the detection limits of 0.02 and 0.03 μM, respectively. In addition, the sensor has the advantages of low cost, high sensitivity, simple preparation and environmental friendliness, as well as good selectivity, stability and reproducibility. We measured AC and LEV in artificial urine, tap water, and lake water, and the recoveries were between 93 % and 109 %, indicating that the sensor has good application prospects in biomedicine and environmental protection.

Binder-free and efficient voltammetric sensor based on Zn-Ca2CuO3 nanoparticles for simultaneous determination of amlodipine, acetaminophen, and ascorbic acid in hypertension patients.

Amlodipine (AM) is a long active calcium channel blocker used to relax blood vessels by preventing calcium ion transport into the vascular walls and its supporting molecules acetaminophen (AP) and ascorbic acid (AA) are recommended for hypertension control and prevention. Considering their therapeutic importance and potential side effects due to over dosage, we have fabricated a sensor for individual and simultaneous determination of AA, AP, and AM in pharmaceuticals and human urine using novel Zn-doped Ca2CuO3 nanoparticles modified glassy carbon electrode (GCE). Optimally doped Ca2CuO3 (2.5 wt% Zn at Cu site) enhanced the detection of target molecules over much wider concentration ranges of 50 to 3130 µM for AA, 0.25 to 417 µM for AP, and 0.8 to 354 µM for AM with the corresponding lowest detection limits of 14 µM, 0.05 µM, and 0.07 µM, respectively. Furthermore, the Zn-Ca2CuO3/GCE exhibited excellent selectivity and high sensitivity even in the presence of several potential interfering agents. The usefulness of the developed electrode was tested using an amlodipine besylate tablet and urine samples of seven hypertension patients under medication. The results confirmed the presence of a significant amount of AP and AM in six patients' urine samples indicating that the personalized medication is essential and the quantum of medication need to be fixed by knowing the excess medicines excreted through urine. Thus, the Zn-Ca2CuO3/GCE with a high recovery percentage and good sensitivity shall be useful in the pharmaceutical and biomedical sectors.

A novel composite electrode based on graphene oxide/MnO2:h‐MoO3 particles for square wave voltammetric determination of acetaminophen

AbstractA novel composite electrode was developed based on graphene oxide (GO)/MnO2:h‐MoO3 nanocomposite for sensitive and selective voltammetric detection of acetaminophen (ACP). The composite electrode materials were characterized using X‐Ray photoelectron spectroscopy (XPS), X‐Ray Diffraction (XRD), scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetric (CV) techniques. In the optimum conditions, the oxidation peak current (Ipa) of ACP was increased linearly with its concentration over two linear ranges from 0.06 to 10.0 μmol L−1 and 20.0 to 80.0 μmol L−1 with a detection limit of 0.0133 μmol L−1. Due to its higher selectivity and long term stability, the composite electrode was applied to the detection of ACP in pharmaceutical formulations.

Fabrication of Strontium Molybdate with Functionalized Carbon Nanotubes for Electrochemical Determination of Antipyretic Drug-Acetaminophen.

In recent years, there has been a significant interest in the advancement of electrochemical sensing platforms to detect antipyretic drugs with high sensitivity and selectivity. The electrochemical determination of acetaminophen (PCT) was studied with strontium molybdate with a functionalized carbon nanotube (SrMoO4@f-CNF) nanocomposite. The SrMoO4@f-CNF nanocomposite was produced by a facial hydrothermal followed by sonochemical treatment, resulting in a significant enhancement in the PCT determination. The sonochemical process was applied to incorporate SrMoO4 nanoparticles over f-CNF, enabling a network-like structure. Moreover, the produced SrMoO4@f-CNF composite structural, morphological, and spectroscopic properties were confirmed with XRD, TEM, and XPS characterizations. The synergistic effect between SrMoO4 and f-CNF contributes to the lowering of the charge transfer resistance (Rct=85 Ω·cm2), a redox potential of Epc=0.15 V and Epa=0.30 V (vs. Ag/AgCl), and a significant limit of detection (1.2 nM) with a wide response range of 0.01-28.48 µM towards the PCT determination. The proposed SrMoO4@f-CNF sensor was studied with differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques and demonstrated remarkable electrochemical properties with a good recovery range in real-sample analysis.

Flexible electrochemical sensor based on a ZnO-doped SnO2 heterojunction for simultaneous electrochemical determination of p-aminophenol and acetaminophen

In this work, a novel flexible electrochemical sensor was successfully developed for the simultaneous determination of p-aminophenol and acetaminophen. The sensor is composed of a methanesulfonic acid-treated poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonic acid) film on a poly(ethylene terephthalate) substrate, which has been modified using a zinc oxide-doped tin oxide heterojunction applied through drop-coating (C-ZnO/SnO2-PEDOT/PET). The oxygen vacancies resulting from zinc oxide-doped tin oxide heterojunctions within highly conductive metal oxide nanomaterials enhance mass transfer and synergize seamlessly with methanesulfonic acid-treated electrically conductive dielectric PEDOT/PET films, leading to a substantial improvement in electrochemical activity. Under the optimal conditions, a wider linear range and lower detection limits were shown for p-aminophenol (2–511 μM, LOD=0.437 μM) and acetaminophen (2–591 μM, LOD=0.562 μM). In addition, the sensors demonstrated high accuracy in detecting p-aminophenol and acetaminophen in real samples, with recoveries of 99.36 %-99.60 % and 97.56 %-99.80 %, respectively. Furthermore, the flexible sensors maintained a superior electrochemical response when detecting p-aminophenol and acetaminophen at different bending angles, with relative standard deviations of 0.62 % and 1.68 %, respectively. These findings suggest potential applications for the development of wearable sensors in the future.

Anthraquinone/activated carbon electrochemical sensor and its application in acetaminophen analysis.

Acetaminophen (AC) can inhibit the synthesis of prostaglandins in the body, and has antipyretic and analgesic effects. In this paper, a two-step microwave impregnation method was used to prepare anthraquinone (AQ)-doped carbon composite, which were applied to the surface modification of glassy carbon electrodes (GCE) for the determination of acetaminophen (AC) using differential pulse voltammetry (DPV). The composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman and Fourier infrared spectroscopy (FT-IR). The results showed that anthraquinone was successfully modified on the surface of activated carbon. The peak current of AC increased with its concentration in the range of 0.1μM to 700μM (R2 = 0.998) and a detection limit of 0.05μM was obtained with 20%AQ doped carbon electrochemical sensor (20%AQ-C/GCE). Electrochemical Impedance Spectroscopy (EIS) test results indicated that the charge transfer resistance (Rct) of 20%AQ-C/GCE is only the one-fourth of that of bare GCE. The proposed 20%AQ-C/GCE sensor has good stability, reproducibility and selectivity for the detection of AC. The sensor is also suitable for the detection of real samples, indicating its good practicality.

Tetragonal arranged BiOCl interconnected with functionalized carbon tubes for a sensitive determination of Acetaminophen

Acetaminophen (AAP) is well recognized as a pharmaceutical agent but prolonged consumption of AAP causes serious health issues for human beings. Herein we focus on BiOCl implanted with functionalized carbon nanotube (f-CNT) used to predict AAP levels in the human body samples by electrochemical detection. Bismuth Oxy Chloride (BiOCl) improves electrochemical performance with its electrochemical active sites, it suffers from sluggish kinetics with electron transfer. The composites of BiOCl and f-CNT are well-dispersed substantially, and the synergistic interface between BiOCl and f-CNT improves the electron transfer properties, alongside the catalytic activity enhanced with the large surface area of f-CNT. Notably, the BiOCl/f-CNT/Glassy carbon electrode (GCE) composite exhibits an excellent redox AAP detection in the electrochemical methods of cyclic voltammetry and different pulse voltammetry in pH-7.0 phosphate buffer solution at 0.4 V. The BiOCl/f-CNT composite achieves an outstanding lower detection limit of 0.0016 µM with a wide linear range of 0.01 to 650 µM of AAP with a higher sensitivity of 0.8754 µA µM−1 cm−2. Moreover, composite additionally depicts good selectivity and outstanding repeatability, reproducibility, and strong stability. However, human urine and blood serum gain insights into the clinical detection of AAP with an Acceptable recovery range.

Multi-walled carbon nanotubes/carbon black/rPLA for high-performance conductive additive manufacturing filament and the simultaneous detection of acetaminophen and phenylephrine

The combination of multi-walled carbon nanotubes (MWCNT) and carbon black (CB) is presented to produce a high-performance electrically conductive recycled additive manufacturing filament. The filament and subsequent additively manufactured electrodes were characterised by TGA, XPS, Raman, and SEM and showed excellent low-temperature flexibility. The MWCNT/CB filament exhibited an improved electrochemical performance compared to an identical in-house produced bespoke filament using only CB. A heterogeneous electrochemical rate constant, kobs0\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${k}_{obs}^0$$\\end{document} of 1.71 (± 0.19) × 10−3 cm s−1 was obtained, showing an almost six times improvement over the commonly used commercial conductive CB/PLA. The filament was successfully tested for the simultaneous determination of acetaminophen and phenylephrine, producing linear ranges of 5–60 and 5–200 μM, sensitivities of 0.05 μA μM−1 and 0.14 μA μM−1, and limits of detection of 0.04 μM and 0.38 μM, respectively. A print-at-home device is presented where a removable lid comprised of rPLA can be placed onto a drinking vessel and the working, counter, and reference components made from our bespoke MWCNT/CB filament. The print-at-home device was successfully used to determine both compounds within real pharmaceutical products, with recoveries between 87 and 120% over a range of three real samples. This work paves the way for fabricating new highly conductive filaments using a combination of carbon materials with different morphologies and physicochemical properties and their application to produce additively manufactured electrodes with greatly improved electrochemical performance.Graphical abstract

Construction of molecularly imprinted voltammetric sensor based on rGO/Ti3C2Tx for the selective determination of acetaminophen

Acetaminophen (AP) is one of the most commonly used nonsteroidal anti-inflammatory and antipyretic analgesics, but overdose of AP can produce toxic metabolite in the body, eventually leading to liver and kidney damage, which make it necessary to detect and control the proper amount. The sensor harnessed a molecularly imprinted polymer (MIP) for selective recognition of AP, and Ti3C2Tx nanosheets modified by rGO for signal amplification. The electrochemical sensing performance of MIP/rGO/Ti3C2Tx electrode toward AP was investigated. Under optimized conditions, the sensor has low detection limit (LOD = 1.58 nM, S/N = 3), wide detection range (10−8−10−3 M), strong selectivity, and good stability. In addition, the sensor can be applied to the AP detection in simulate real samples, which provides an effective method and a useful way for the application of new 2D nanomaterials in the field of sensing.

The Effect of Slicer Infill Pattern on the Electrochemical Performance of Additively Manufactured Electrodes

AbstractIn this work we report the dramatic effects that changing the infill pattern has on the electrochemical performance of an additively manufactured electrode made from commercial filament. Electrodes were produced using six different slicing patterns and imaged to confirm how the infill pattern altered the working electrode surface. These electrodes were then electrochemically characterised against the near‐ideal outer sphere redox probe [Ru(NH3)6]3+, the common inner sphere probe [Fe(CN)6]3−, and then used for the electroanalytical determination of acetaminophen. It was found that changing the infill pattern had a dramatic effect on the electrochemical performance of the electrodes. Over the course of the manuscript, it can be seen that Aligned Rectilinear and Rectilinear infill patterns perform consistently well and offer good reproducibility. On the other hand, Concentric infill pattern had noticeably poor inter‐electrode reproducibility and the Hilbert Curve infill was one of the worst performing electrodes in many categories. For future work in this field, we recommend the infill pattern is always reported within the experimental section to allow other researchers to repeat work properly. Additionally, when optimising an electroanalytical sensing platform, we encourage researchers to optimise the infill pattern as it has direct influence on the analytical parameters.

Wavelength-dependent photoelectrochemical response demonstrated by the determination of acetaminophen and rutin in differential molecularly imprinted polymers strategy

Herein, the excitation wavelength-dependent responses of the molecularly imprinted polymer (MIP) photoelectrochemical (PEC) sensors were investigated, using acetaminophen (AP), rutin (RT) and perfluorooctanoate (PFOA) as the model templates, pyrrole as functional monomer, CuInS2@ZnS/TiO2 NTs as the basic photoelectrode. With wavelength λ > 240 nm, the photocurrent of MIPPFOA enhanced at higher concentrations of PFOA. With increasing AP concentration, the photocurrents of MIPAP could decline with λ < 271 nm, not change at λ = 270 nm, or increase with λ > 270 nm. As RT concentration increased, the photocurrents of MIPRT could decrease (λ < 431 nm), not change (λ = 431 nm) or increase (λ > 431 nm). The PEC responses depend on the comprehensive interaction of two contrary mechanisms from the template molecules within the MIP membrane. The photocurrent is enhanced by the role of the electron donor for photo-generated holes but attenuated due to the steric hindrance effect and the excitation light intensity loss via absorption or scattering. The apparent molar absorption coefficient of AP and RT within MIP membranes are 9.1–19.4 folds of those measured from dilute solutions. By using a routine UV lamp as the light source, the photocurrents of MIPRT at 254 nm and MIPAP at 365 nm were used to determine RT and AP, with the detection limits of 5.3 and 16 nM, respectively. The interference from the non-specific adsorption of interferents on the surfaces of MIPAP and MIPRT was reduced by one order of magnitude via a differential strategy.

Synchronous analysis of acetaminophen, codeine, and caffeine in human fluids employing graphite screen-printed electrodes.

A facile electrochemical approach is proposed for the synchronous determination of acetaminophen (ACP), codeine (COD) and caffeine (CAF) utilizing unmodified screen-printed electrodes (SPEs). The determination of ACP, COD and CAF has been explored across different supporting electrolytes including sulfuric acid (H2SO4), hydrochloric acid (HCl), phosphoric acid (H3PO4) and Briton Robinson (B.R) buffer solutions. It was found that a 0.05 mol L-1 sulfuric acid solution is an optimal supporting electrolyte utilized for voltammetric analysis of ACP, COD, and CAF with improved sensitivity, stability, and reproducibility. The electro-analytical sensing of ACP, COD and CAF was investigated using SPEs within linear concentration ranges of 3.0-35.0 μmol L-1, 10-160 μmol L-1 and 10-160 μmol L-1 and revealed competitively low limits of detection (3S/N) of 0.9, 4.8 and 6.3 μmol L-1 for ACP, COD and CAF, respectively. The results indicated the possibility of such a simple and quick electroanalytical protocol for online monitoring of pharmaceutical formulations comprising ACP, COD, and CAF drugs in human fluids with satisfactory recovery.

A systematic review on electrochemical sensors for the detection of acetaminophen.

Considerable progress has been made in the electrochemical determination of acetaminophen (AP) over the past few decades. Nanomaterials or enzymes as electrode modifiers greatly improve the performance of AP electrochemical sensors. This review focuses on the development potential, detection principles and techniques for the electrochemical analysis of AP. In particular, the design and construction of AP electrochemical sensors are discussed from the perspective of non-enzyme materials (such as nanomaterials, including precious metals, transition metals and non-metals) and enzyme substances (such as aryl acylamidase, polyphenol oxidase and horseradish peroxidase). Moreover, the influencing factors for AP electrochemical sensors and the simultaneous detection of AP and other targets are summarized, and the future prospective of AP electrochemical sensors is outlined. This review provides a reference and guidance for the development and application of electrochemical sensors for AP detection.