Determination of salicylic acid content in pharmaceuticals using chitosan@Fe3O4/CPE electrode detected by SWV technique.

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2023-01-01 DOI:10.5599/admet.1682
Sudarut Pitakrut, Phetlada Sanchayanukun, Sasithorn Muncharoen
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Abstract

Chitosan-coated magnetite nanoparticles (Chitosan@Fe3O4) were used to modify the carbon paste electrode (Chitosan@Fe3O4/CPE) to enhance sensitivity for salicylic acid (SA) analysis using square wave voltammetry (SWV). The performance and behaviour of the purposed electrodes were investigated using cyclic voltammetry (CV). The results showed that the mixed behaviour process was observed. Furthermore, parameters affecting SWV were also studied. It was discovered that the optimum conditions were a two-linearity range of SA determination, 1-100 and 100-400 μM. The limit of detection (LOD) and the limit of quantitation (LOQ) for SA are 0.57 μM and 0.90 μM, respectively. The proposed electrodes were successfully used to determine SA in applications employing pharmaceutical samples.

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SWV技术检测chitosan@Fe3O4/CPE电极测定药品中水杨酸含量。
利用壳聚糖包覆磁铁矿纳米颗粒(Chitosan@Fe3O4)修饰碳膏电极(Chitosan@Fe3O4/CPE),提高方波伏安法(SWV)分析水杨酸(SA)的灵敏度。用循环伏安法(CV)研究了电极的性能和行为。结果表明,该材料存在混合行为过程。此外,还研究了影响SWV的参数。结果表明,测定SA的最佳条件为1 ~ 100 μM和100 ~ 400 μM的双线性范围。SA的检测限和定量限分别为0.57 μM和0.90 μM。所提出的电极成功地用于测定药物样品中的SA。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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