Differential Pulse Voltammetry Research Articles

Determination of methotrexate using carbon paste electrode modified with ionic liquid/Ni-Co layered double hydroxide nanosheets as a voltammetric sensor.

Methotrexate (MTX) is a widely used anti-cancer drug, but its overuse can lead to significant side effects. Therefore, it is very vital to design simple and sensitive analytical methods for its determination. In this work, an electrochemical sensor was prepared based on an ionic liquid (IL)/Ni-Co layered double hydroxide nanosheets (Ni-Co-LDH)-modified carbon paste electrode IL/Ni-Co-LDH/CPE. Cyclic voltammetry, differential pulse voltammetry, and chronoamperometry methods were applied to evaluate the performance of the designed sensor for MTX determination. The IL/Ni-Co-LDH/CPE sensor exhibits a linear relationship between the peak current of the differential pulse voltammetry and MTX concentrations in the linear dynamic range of 0.02 to 140.0 μM, with a detection limit of 0.006 μM. The IL/Ni-Co-LDH/CPE sensor exhibited relative standard deviation values between 1.7 to 3.7 % for recovery tests on real samples, indicating the precision of the method. The designed sensor with cost-effective and good performance could be valuable for therapeutic drug monitoring and clinical diagnostics.

ZrO2 Nanofiber-Based Molecular Imprinted Electrochemical Sensor for Detection of Ampicillin

An efficient molecularly-imprinted electrochemical sensor for the detection of ampicillin was prepared using polypyrrole tetracycline polymer modified with ZrO2 nanofibers. The ZrO2 nanofibers prepared by electrostatic spinning increased the surface area of the electrode with the binding sites of the electropolymerized membrane. The ampicillin sensor with polypyrrole as the functional monomer was able to specifically bind ampicillin molecules and detect ampicillin in various types of samples. In this study, cyclic voltammetry and differential pulse voltammetry were used to evaluate the electrochemical performance of ZrO2-MIP. Under the optimized conditions, the detection limit of this sensor was 0.397 nM, the detection range was 0.5 ∼ 500 nM, and the R2 reached 0.998. It has good selectivity, reproducibility, and stability, and achieves the AMP detection of the milk of the actual samples, which has a good prospect of application.

Eco-Friendly Voltammetric Analysis of Flibanserin with Electropolymerized β-Cyclodextrin on Carbon Sensors

This study developed a cost-effective method to determine flibanserin (FLN) using a screen-printed carbon electrode modified with β-Cyclodextrin polymer (SPCE/β-CD). The electrode was modified in Britton-Robinson buffer at pH 5.0 to enhance FLN’s electrochemical oxidation, with cyclic and differential pulse voltammetry used for detection. Characterization techniques included energy-dispersive X-ray analysis, scanning electron microscopy, and Fourier transform infrared spectroscopy. The method showed a linear response to FLN concentrations ranging from 5.2 to 80.0 ng ml−1, with a detection limit of 0.004 μM and a quantitation limit of 0.014 μM. The modified electrode demonstrated good sensitivity, reproducibility, and was applied successfully to FLN analysis in spiked human serum and urine samples. An environmental impact assessment was conducted using the Green Analytical Procedure Index, which evaluates the green characteristics of the entire analytical methodology from sample collection to final determination. Additionally, the Analytical Eco-Scale, which assesses the use of organic preparations, procedures, and instruments, demonstrated a favorable green analysis profile. This modified electrode provides a convenient, cost-effective, and eco-friendly approach for determining flibanserin in various matrices.

Functional designed S-doped FeWO4 hybrid for efficient mebendazole electro-oxidation and photodegradation of Methylene Blue

Sulfur-doped FeWO4 nanoparticles were synthesized via co-precipitation followed by the calcination method. The prepared samples were characterized by various techniques such as XR, FTIR, SEM, TEM, UV-DRS, PL, XPS and CV. The XRD analysis confirmed the characteristic suggesting the monoclinic phase of the S doped FeWO4. In contrast, the flower like rod like morphology found from SEM and TEM. Additionally, the study determined the optimal parameters for achieving maximum degradation of Methylene Blue (MB) dye. The most significant degradation percentage occurred when utilizing 50 mg of S-doped FeWO4 nanoparticles per 100 mL of MB solution, exposed to visible light for 70 min. Subsequently, the Mebendazole (MBZ) drug was detected using differential pulse voltammetry, employing an S-doped FeWO4 modified GCE as working electrode. Linear responses to the MBZ drug within the absorption collection of 0.1 × 10-8 to 12.4 × 10-9 M were observed, showing a sensitivity of 4.563 µA/10-8M. The detection limit (DL) and quantification limit (QL) were calculated as 5.11 nM µA-1 and 17.54 nM µA-1, respectively, with signal-to-noise ratios of S/N=3. Finally, it shows that s-doped FeWO4 esterification process, the S-doped FeWO4 catalyst was effectively functional to create benzoic acid and convert it to ester from benzoic acid, ethanol, and H2SO4 acid for organic heterogeneous catalyst.

Electrochemical Detection of Tobramycin Resistance in Escherichia Coli

The development of techniques to detect the presence of resistance in pathogens are urgently needed to face the deadly spread of multi-drug-resistant bacteria. The present work presents the electroanalytical quantification of tobramycin (TOB) retention in susceptible and resistant bacterial strains of Escherichia coli. The electrochemical characterization of TOB demonstrates the suitability of electrochemistry for drug detection. Differential pulse voltammetry (DPV) parameters were optimized by full factor experimental designs, which increased two-times the electrochemical current response, improving the overall sensitivity of the method. The developed assay was able to differentiate between resistant and susceptible E. coli strains within 15 min. The demonstrated methodology is expected to be applicable to both drug efflux-mediated and drug uptake inhibition-mediated resistant bacteria. Because these two mechanisms represent the most predominant reasons for drug resistance in bacteria, the reported method has a strong potential to be a reliable, fast, and cost-efficient alternative for antibiotic resistance detection.

Study on the electrochemical and spectroscopic characteristics of holmium ion and its interaction with DNA

Metal ion-DNA interactions play a crucial role in modulating the structure and function of genetic material in the natural environment. In this study, we report on the favorable electrochemical activity of holmium(III) (Ho3+) on a glassy carbon electrode (GCE) and its interaction with double-stranded DNA. The interaction between DNA and Ho3+ was investigated for the first time using cyclic voltammetry and differential pulse voltammetry. The electrochemical behavior of Ho3+ ions on a GCE exhibited a reversible electron transfer process, indicative of its redox activity. A linear correlation between the peak current and the square root of the scan rate was observed, suggesting a diffusion-controlled kinetic regime for the electrochemical process. Additionally, fluorescence and absorption spectroscopy were employed to confirm the binding of Ho3+ to DNA. Our findings demonstrate that, at pH 7.2, specific DNA bases and phosphate groups can interact with Ho3+ ions. Moreover, electrochemical measurements suggest that Ho3+ ions bind to DNA via a groove binding mode, with a calculated binding ratio of 1:1 between Ho3+ and DNA. Notably, under optimal conditions, an increase in the amount of DNA leads to a significant reduction in the current intensity of Ho3+ ions.

A Novel, Selective, and Fast Electrochemical Sensor Based on an 8-Nitroquinoline-Coated Pencil Graphite Electrode for Rutin Determination in Orange Juice

In this study, we developed a facile and low-cost method to prepare a modified electrode by coating the pencil graphite electrode (PGE) surface with 8-nitroquinoline (8-NQ). The surface modification process was carried out by electrochemical reduction of 8-NQ on the PGE surface in ethanol solution. The optimum conditions were determined for the experimental studies. The differential pulse voltammetry was used to determine rutin with the modified electrode (8-NQ/PGE). The developed electrode showed excellent performance for rutin oxidation in a pH 3.0 Britton Robinson buffer (BR). In this media, linearly increasing anodic peak currents were observed with the concentration of rutin in two wide concentration ranges (i.e., 0.016–0.96 μM and 0.96‒19.73 μM), the sensor showed a low detection limit (i.e., 4.14 nM) (3 s m−1). It displayed good stability and selectivity. Also, it was used successfully for the determination of rutin in orange juice samples.

Ferrocene Derivatives Modified MOFs-Based Sensors for Electrochemical Detection of Chloramphenicol

Although chloramphenicol(CAP) plays a critical role in many medical treatments, its abuse is not only seriously toxic to humans but also ecologically harmful when discharged into the water. Therefore, it is of great significance to realize the rapid and efficient detection of CAP. 2D MOFs Cu3(HITP)2 (HITP = 2,3,6,7,10,11-hexaiminotriphenylene) with higher electrical conductivity than conventional MOFs were synthesized using hydrothermal methods. Fc-NH2, as an electron donor, was dispersed on the surface of MOFs by physical doping. The synthesized nanocomposite Cu3(HITP)2/Fc-NH2 has excellent adsorption properties and electrical conductivity. It was used to construct an electrochemical sensor and exhibited superior performance in the detection of CAP. Electrochemical reduction of CAP on Cu3(HITP)2/Fc-NH2/GCE was investigated using cyclic voltammetry and differential pulse voltammetry. The results show that Cu3(HITP)2/Fc-NH2/GCE has a much wider linear range of 0.5 ∼ 2100 μm than previous studies when detecting CAP. The detection limit is as low as 0.43 μm. The electrochemical sensing platform reported in this work also exhibits excellent reproducibility, selectivity, and stability, and the recovery rate of CAP detection in the actual sample ranged from 97.1% to 102.4%. This work provides a new strategy for antibiotic detection and extends the application of triphenylene-based MOFs in the electrochemical sensing field.

Ultrasonically assisted fabrication of electrochemical platform for tinidazole detection

Based on sonochemistry, green synthesis methods play an important role in the development of nanomaterials. In this work, a novel chitosan modified MnMoO4/g-C3N4 (MnMoO4/g-C3N4/CHIT) was developed using ultrasonic cell disruptor (500 W, 30 kHz) for ultra-sensitive electrochemical detection of tinidazole (TNZ) in the environment. The morphology and surface properties of the synthesized MnMoO4/g-C3N4/CHIT electrode were characterized using X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM) and transmission electron microscope (TEM). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were utilized to assess the electrochemical performance of TNZ. The results indicate that the electrochemical detection performance of TNZ is highly efficient, with a detection limit (LOD) of 3.78 nM, sensitivity of 1.320 µA·µM−1·cm−2, and a detection range of 0.1–200 μM. Additionally, the prepared electrode exhibits excellent selectivity, desirable anti-interference capability, and decent stability. MnMoO4/g-C3N4/CHIT can be successfully employed to detect TNZ in both the Songhua River and tap water, achieving good recovery rates within the range of 93.0 % to 106.6 %. Consequently, MnMoO4/g-C3N4/CHIT’s simple synthesis might provide a new electrode for the sensitive, repeatable, and selective measurement of TNZ in real-time applications. Using the MnMoO4/g-C3N4/CHIT electrode can effectively monitor and detect the concentration of TNZ in environmental water, guiding the sewage treatment process and reducing the pollution level of antibiotics in the water environment.

Oxygen‐Doped Graphitic Carbon Nitride for Electrochemical Uric Acid Sensing: Method Without Metals

AbstractThe present study examined potential benefits of heteroatom doping to manipulate the electrical structure and to enhance the efficiency of the sensor, with an emphasis on developing inexpensive, metal‐free electrochemical sensors. Melamine and ammonium oxalate were used as precursors in a one‐step thermal polymerization technique yielding oxygen‐doped graphitic carbon nitride (O‐gCN). Following synthesis, the material's structural and morphological properties were thoroughly examined using a multitude of analytical techniques, including EIS. A notable decrease in impedance was observed, suggesting improved conductivity. Additionally, the doping approach exhibited a noticeable improvement in reduction current receptivity and surface area as compared to unmodified graphitic carbon nitride (g‐CN). Utilizing both differential pulse voltammetry (DPV) and the classical cyclic voltammetry (CV) methods, we investigated the electro oxidation of uric acid (UA) as well as concentration dependence and selectivity studies using oxygen‐doped graphitic carbon nitride modified glassy carbon electrode (O‐gCN@GCE). O‐gCN@GCE demonstrated remarkable performance, allowing the detection of UA concentrations as low as 7.784 µAµM−1cm−2. Its low detection limit of 0.57 µM and wider linear range (5–120 µM) further highlighted its potential for extremely sensitive assays and its remarkable capacity to operate over a broad UA concentration range.

MoS2_CNTs_aerogel-based PEDOT nanocomposite electrochemical sensor for simultaneous detection of chloramphenicol and furazolidone in food samples

Toxic intermediates in food caused by chloramphenicol (CP) and furazolidone (FZ) have gained interest in research toward their detection. Hence, fast, reliable, and accurate detection of CP and FZ in food products is of utmost importance. Here, a novel molybdenum disulfide-connected carbon nanotube aerogel/poly (3,4-ethylenedioxythiophene) [MoS2/CNTs aerogel/PEDOT] nanocomposite materials are constructed and deposited on the pretreated carbon paste electrode (PCPE) by a facile eletropolymerization method. The characterization of MoS2/CNTs aerogel/PEDOT nanocomposite was analyzed by scanning electron microscopy (SEM), cyclic voltammetry, and differential pulse voltammetry. The modified MoS2/CNTs aerogel/PEDOT nanocomposite has improved sensing characteristics for detecting CP and FZ in PBS solution. For this work, we have studied various parameters like electrocatalytic activity, the effect of scan rates, pH variation studies, and concentration variation studies. Under optimum conditions, the modified electrode exhibited superior sensing ability compared to the bare and pretreated CPE. This improvement in electrocatalytic activity can be the higher conductivity, larger surface area, increased heterogeneous rate constant, and presence of more active sites in the MoS2/CNTs aerogel/PEDOT nanocomposite. The modified electrode demonstrated distinct electrochemical sensing toward the individual and simultaneous analysis of CP and FZ with a high sensitivity of 0.701 µA. µM−1 .cm−2 for CP and 0.787 µA. µM−1 .cm−2 for FZ and a low detection limit of 3.74 nM for CP and 3.83 nM for FZ with good reproducibility, repeatability, and interferences. Additionally, the prepared sensor effectively detects CP and FZ in food samples (honey and milk) with an acceptable recovery range and a relative standard deviation below 4%.

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.

Addressing the Challenge of a Simultaneous Destructive Assay of Plutonium and Uranium: Highly Precise, Robust, Universal, and Reagent-Free Differential Pulse Voltametric Method Development in Biodegradable Methanesulfonic Acid Medium.

The destructive assay of bulk uranium and plutonium, a cornerstone for chemical quality control and nuclear material accounting of fuel matrices, mandates robust and precise methodologies. Despite ongoing research, simultaneous, matrix independent determination of U and Pu has eluded solution owing to inherent limitations in aqueous acid medium, viz., coexistence of multiple oxidation states, coupled electrochemical reactions, smaller potential window, and requirement for multistep sample preconditioning and tedious electrode modification. The present study addresses this challenge wherein non-aqueous methanesulfonic acid (MSA) served the dual role of solvent and analyte media with a bare glassy carbon (GC) electrode. Fuel matrices, viz., (U, Pu)C, (U, Pu)O2, PuO2, UO3, UO2, and U3O8, were quantitatively dissolved in biodegradable MSA, without using any additives. Redox speciation of the analytes, U and Pu, in MSA was probed by ultraviolet-visible spectrophotometry and electrometry, revealing the absence of electrocatalytic regeneration and stabilization of single oxidation state, viz., U(VI) and Pu(IV), along with relevant redox-energetic (electron transfer and reversibility) and kinetic data. Bidentate coordination of MSA with the U analyte was indicated by X-ray absorption spectroscopy studies and was corroborated by density functional theory-based investigations, providing the optimized structure, viz., [UO2(MSA)2] and [Pu(MSA)4], binding modes and energy, partial charges, and molecular orbital diagrams. Based on these insights, the feasibility of differential pulse voltammetry (DPV)-based assay method development for U and Pu separately and in different U/Pu ratios, representing assorted fuel matrices, was probed. Analytical figures of merit for both U and Pu (detection limit of ∼10-5 M, precision of ∼0.2%, accuracy of ∼0.2%, high sensitivity, repeatability, and non-influence of relevant interferences) were determined, method validated employing actual fuel samples, and compared with the established, multi-step biamperometry method. Hence, a universal, simultaneous U and Pu destructive assay method in non-aqueous MSA media based on DPV with a commercial GC electrode was demonstrated.

Intelligent machine learning enabled sensor for acyclovir using NiMnO3 flower-like electrocatalyst

Hierarchical flower-like NiMnO3 was prepared using a hydrothermal route for oxidative detection of acyclovir (ACV), an antiviral pharmaceutical pollutant. The flower-like structure with an electroactive surface area (EASA) of 0.0952 cm2 enables non-revisable oxidation of ACV, with differential pulse voltammetry (DPV) and amperometry confirming its robust analytical capability in both high (15–75 µM) and low (0.1–1.0 µM) concentration ranges, respectively. Using amperometry, the sensor achieved an estimated limit of detection (LOD) of 1.59 nM (S/N=3) with selective oxidation of ACV and a sensitivity of 1.039µA µM−1 cm2 in the presence of other common interferants. The adaptation of machine learning (ML) algorithms like random forest, XGBoost, linear regression, and ANN validated sensors’ performance and confirmed ANN’s superiority in DPV signal interpretation. NiMnO3, as an electrocatalyst for ACV oxidation, validated by ANN modeling, highlights bimetallic oxides’ potential as a cost-effective, versatile platform for detecting pharmaceutical pollutants.

Ruthenium-based microstructures modified by gold particles as composite electrode material for non-enzymatic epinephrine detection

A simple and efficient technique for voltammetric enzymeless detection of epinephrine (EP) was proposed. In this technique, we applied hierarchical Ru-based electrode modified by Au nano- to micro-sized particles that was fabricated using laser-assisted synthesis. The cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were employed to characterize electrochemical properties of the fabricated electrode material. For EP detection, we obtained two DPV calibration curves that were linear in the range of 0.05–5 μM and 5–500 μM. The highest sensitivity (45.0 μA μM−1 cm−2) and the lowest detection limit (6.4 nM) were observed for the first linear range, whereas the estimated sensitivity and limit of detection for the second linear range were 2.0 μA μM−1 cm−2 and 18.7 nM, respectively. We also demonstrated that the proposed technique can be used for selective EP determination in the presence of such common interfering analytes as ascorbic acid and dopamine. The results of this study can be potentially used for development of low-cost voltammetric sensor platforms for non-enzymatic epinephrine detection.

Magnetic Porous Hydrogel-Enhanced Wearable Patch Sensor for Sweat Zinc Ion Monitoring.

Wearable sensors for sweat trace metal monitoring have the challenges of effective sweat collection and the real-time recording of detection signals. The existing detection technologies are implemented by generating enough sweat through exercise, which makes detecting trace metals in sweat cumbersome. Generally, it takes around 20 min to obtain enough sweat, resulting in dallied and prolonged detection signals that cannot reflect the endogenous fluctuations of the body. To solve these problems, we prepared a multifunctional hydrogel as an electrolyte and combined it with a flexible patch electrode to realize real-time monitoring of sweat Zn2+. Such hydrogel has magnetic and porous properties, and the porous structure of hydrogel enables a fast absorption of sweat, and the magnetic property of the addition of fabricated Fe3O4 NPs not only improves the conductivity but also ensures the adjustable internal structures of the hydrogel. Such a sensing platform for sweat Zn2+ monitoring shows a satisfied linear relationship in the concentration range of 0.16-16 µg/mL via differential pulsed anodic striping voltammetry (DPASV) and successfully detects the sweat Zn2+ of four volunteers during exercise and resting, displaying a promising path for commercial application.

Experiments and Calculation on New N,N-bis-Tetrahydroacridines.

Tetrahydroacridines arouse particular interest due to the potential possibilities of application in the medical field and protection against corrosion. Bis-tetrahydroacridines were newly synthesized by Pfitzinger condensation of 5,5'-(ethane-1,2-diyl) diindoline-2,3-dione with several cyclanones. NMR, MS, and FT-IR were used to prove their molecular structure. In addition, a computer-aided study was performed for the lowest energy conformers of each structure, in vacuum conditions, at ground state using DFT models to assess their electronic properties. UV-Vis and voltammetric methods (cyclic voltammetry, differential pulse voltammetry, and rotating disk electrode voltammetry) were used to investigate their optical and electrochemical properties. The results obtained for these π-conjugated heteroaromatic compounds lead to the conclusion that they have real potential in applications in different fields such as pharmaceuticals and especially as corrosion inhibitors.

The electrochemical properties of bimetallic silver-gold nanoparticles nano film's

Electrode modification has been one of the most active areas of interest in electrochemistry research. Hence, the investigation of the effects of chemically and electrochemically modified GCE nano-films on the NPs electrochemical properties. The electrochemistry of nano-films of Ag NPs, Au NPs and bimetallic Ag-Au (1:2) NPs of chemical citrate reduction synthesis drop coated (DCT) and electro-deposition method (EDP) are reported. The Chemically synthesized NPs were confirmed through FT-IR, UV–visible, XRD and SEM techniques while electro-deposited NPs were ascertained by double-pulsed chrono-amperometry and electrochemical impedance spectroscopy (EIS). The nano films; GCE/Ag NPs, GCE/Au NPs and GCE/Ag-Ag (1:2) NPs in 0.1 M HCl supporting electrolyte were studied via Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) techniques. Generally the DCT nano films were electrochemically superior to the EDP film in terms of current intensities and GCE/Ag-Au (1:2) NPs showed enhanced α (0.019), ks (0.01 s−1), Q (3.6 × 10−9 C), Γ (5.3 × 10−13molescm−2) and D (1.31 × 10−1 cm2s−1), indicating better physicochemical properties for possible sensing applications compared to electro-deposited GCE nano-films.

Innovative voltammetric techniques for bumadizone analysis in pharmaceutical and biological samples: emphasizing green, white, and blue analytical approaches

There are no documented electroanalytical methods for quantifying the anti-inflammatory drug bumadizone (BUM) in pharmaceutical or biological matrices. So, a new voltammetric method was developed to determine BUM at nano concentrations in pharmaceutical forms, in the presence of its alkaline degradant, and in biological fluids. Five electrodes were tested, including three nano-reduced graphene oxide (nRGO) electrodes (5%, 15%, and 20%), a carbon paste electrode (CPE), and a 10% nRGO-modified CPE. The 10% nRGO-modified electrode showed the best performance, offering high selectivity and low detection limits, with good linearity in the concentration range of 0.9 × 102 to 15 × 102 ng mL−1. Differential pulse voltammetry successfully applied this electrode for BUM determination in various samples, achieving excellent recovery without preliminary separation. The method was validated according to ICH guidelines and compared favorably to the reference method. Its environmental impact was assessed using AGREE and Eco-scale metrics in addition to the RGB algorithm, showing superior greenness and whiteness profiles due to safer solvents and lower energy consumption, along with high practical effectiveness using the BAGI metric.

Synthesis and characterization of a novel GaN – Poly (3,4-ethylene dioxythiophene)-Poly(thiophene) Hybrid Nanocomposite: Dual functionality as an electrocatalyst for OFZ and photocatalyst for methylene blue degradation

We introduce GaN-PEDOT-PTh, a groundbreaking hybrid nanomaterial synthesized via a two-step process involving ammonolysis and chemical oxidative techniques. The successful formation of core–shell structures underscores the adaptability of the GaN-PEDOT-PTh approach, particularly in enhancing photocatalytic performance. These characteristics significantly elevate its catalytic efficiency, as notably demonstrated by the rapid degradation of methyl blue (MB). Impressively, the hybrid achieves a 95.77 % MB degradation rate within just 80 min, attributed to its effective suppression of rapid electron-hole recombination, thereby amplifying overall photocatalytic activity. Furthermore, we utilized differential pulse voltammetry to detect the OFZ (OFZ) drug, employing a GaN-PEDOT-PTh-modified GCE as the working electrode. Linear responses to OFZ within the concentration range of 0.3 × 10−7 to 4.1 × 10−8 M were observed, demonstrating sensitivities with detection limits (DL) and quantification limits (QL) of 23.52 × 10−8 M µA−1 and 78.33 × 10−8 M µA−1, respectively.