Chromium oxide nanoparticles as a modifier of carbon paste electrode for cyclic voltametric assessment of paracetamol in medicinal sample

氧化铬纳米颗粒作为碳糊电极的修饰剂,用于循环伏安法测定药物样品中的对乙酰氨基酚

阅读:1

Abstract

The development of novel electrochemical sensors has attracted significant interest in detecting pharmaceutical compounds with high sensitivity and selectivity. Chromium oxide nanoparticles (Cr₂O₃ NPs) are promising materials for modifying carbon paste electrodes (CPEs) due to their excellent electrochemical properties and conductivity. The Cr(2)O(3) NPs were synthesized by the combustion method using, chromium (III) nitrate and glycine at 350 ℃. The microstructure of the Cr(2)O(3) NPs was examined using Field emission scanning electron microscopy (FESEM). The phase composition of the NPs was established using X-ray diffraction spectroscopy (XRD). Raman Spectroscopy focused on the crystallinity of the NPs. Energy dispersive X-ray spectroscopy (EDS) gives the elemental composition. The surface structure of the bare carbon paste electrode (BCPE), was modified with a Chromium oxide composite carbon paste electrode (CrCCPE), and then by the immobilization process of the addition of Cetyl trimethyl ammonium bromide (CTAB) on the electrode fabricated as CTAB modified Cr(2)O(3) composite carbon paste electrode (CT-MCrCCPE) are confirmed by Scanning electron microscopy (SEM). The properties of the modified electrode (CT-MCrCCPE) were investigated for the detection of paracetamol (PA) in a phosphate buffer (PBS) at 6.5 pH using cyclic voltammetry (CV), Electrochemical impedance spectroscopy (EIS) and Differential pulse voltammetry (DPV). The diffusion control process was confirmed by the variation in scan rate (SR), and DPV analysis showed good detection limit (DL) and quantification limit (QL) found as 0.322µM and 1.076µM. PA detection showed selectivity even with interfering ions and achieved 95.37-99.33% accuracy in real sample analysis. CT-MCrCCPE reveals high catalytic activity, sensitivity, selectivity, repeatability, and reproducibility for paracetamol detection.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。