ABSTRACT
Novel tetra-2-(biphenyl-4-yl)-1,3-benzoxazol-carboxamide nickel(II) phthalocyanine (NiTBPBXCAPc) and rGO were confirmed using FT-IR, UV-vis, XRD, TGA and Raman spectra. The NiTBPBXCAPc and rGO nanocomposite has been developed to detect hydroquinone (HQN) and chloramphenicol (CPC). NiTBPBXCAPc has been examined using cyclic voltammetry (CV), linear sweep voltammetry (LSV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS) analysis. The simultaneous CV analysis of HQN and CPC demonstrated the ability of NiTBPBXCAPc@rGO/GCE to execute simultaneous redox reactions. The voltammetric and amperometric limit of detection for HQN and CPC was determined to be 4.5 and 3.5 nM respectively, with a sensitivity of 0.446 and 0.416 µA M-1 cm-2. The amperometric LOD was observed to be 5 and 4 nM with a sensitivity of 0.235 and 0.288 µA M-1 cm-2. Additionally, the NiTBPBXCAPc@rGO/GC electrode is also used for real sample analysis with outstanding recovery. The long-term storage stability, reusability, and real-world sample analysis of the NiTBPBXCAPc@rGO/GC electrode demonstrated its use in environmental analysis.
ABSTRACT
In this report, synthetic and nitro groups containing antibiotic drug nitrofurantoin (NFT) were electrochemically quantified under amended conditions using novel constructed calcium tungstate microspheres modified on glassy carbon electrodes (CTMs/GCE). The calcium tungstate microspheres (CTMs) were synthesized by a facile sonochemical method and characterizations were done by various techniques, such as X-ray diffraction spectrometry (XRD), Fourier transform infrared spectroscopy (FTIR), Raman, field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Ahead of this, electrochemical investigations were performed using electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), amperometry, and linear sweep voltammetry (LSV). The synthesis of CTMs as well-distributed microspheres allows more active metal sites regarding and remarkable electrocatalytic activity towards NFT detection with excellent sensitivity (0.724 µA µM-1 cm-2) and low detection limit (21 nmol L-1) with a wide linear range 10-140 µM. The practical feasibility of the developed CTMs/GC electrode was elucidated using distinct real sample river tap water and clinical sample (NFT capsule), and thus, the modified electrode manifested acceptable recovery results.
Subject(s)
Anti-Bacterial Agents , Nitrofurantoin , Microspheres , Spectroscopy, Fourier Transform InfraredABSTRACT
In the realm of electrochemical sensor application, the development and fabrication of semiconducting metal oxides with the integration of conducting polymers for the trace-level detection of pharmaceutical medicines garnered considerable interest. Herein, we reported facile cadmium oxide decorated with polypyrrole nanotubes fabricated on a glassy carbon electrode (CdO@PPy/GCE) for efficient determination of antihistamine drug promethazine hydrochloride (PMH). The as-synthesized CdO@PPy composite was characterized by various analytical tools like X-ray powder diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. Furthermore, the electrocatalytic activity of the modified electrode for PMH detection was examined by voltammetry and amperometric methods, and the modified electrode exhibited lower charge transfer resistance compared to the bare GCE. Under the optimized condition, the fabricated electrode shows a wide linear range (50-550 µM), better sensitivity (0.13 µAµM-1 cm-2), low detection limit (10.83 nM) (S/N = 3), and excellent selectivity and reproducibility toward PMH detection. Moreover, the modified GCE depicted eminent practical ability for PMH detection in lake water and pharmaceutical tablets.