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抗低血压药物的电分析传感:在剂型和人体尿液中的应用。

Electro-analytical sensing of anti-hypotensive agents: application to dosage forms and human urine.

作者信息

Alharthi Sarah, Batakoushy Hany A, Alharthy Saif A, Abd El-Magied Mahmoud O, Salem Waheed M

机构信息

Department of Chemistry, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.

Pharmaceutical Analysis Department, Faculty of Pharmacy, Menoufia University, Shebin El-Kom, Menoufia 32511, Egypt.

出版信息

Toxicol Res (Camb). 2022 Feb 7;11(1):245-254. doi: 10.1093/toxres/tfac004. eCollection 2022 Feb.

Abstract

A new and valid method was developed for the quantitative voltammetric analysis of midodrine hydrochloride (MID) in pharmaceutical tablets (Midodrine) and biological samples. The method is based on electro-oxidation of MID supported by both disposable pencil electrode (PE) and glassy carbon electrode (GCE). The analysis was carried out using cyclic voltammetry, differential pulse voltammetry (DPV), and square wave voltammetry (SWV) techniques. The proposed analytical method was validated according to ICH guidelines. MID was successively assayed at concentration ranges of 1.15-6.55 and 0.58-3.05 μg mL at PE. Also, MID was successively assayed at concentration ranges of 1.15-5.28 and 2.86-27.6 μg mL at GCE for DPV and SWV methods, respectively. The proposed method was successfully used for the analysis of MID in its dosage form and human urine with good recoveries of 99.66 ± 0.33, 99.8 ± 0.45 at PE and 99.8 ± 0.25, 98.7 ± 1.27 at GCE for the DPV and SWV methods, respectively. The suggested method could be applied to the studied drug in the quality control lab as well as in its pharmacokinetic studies.

摘要

开发了一种用于定量伏安分析药物片剂(米多君)和生物样品中盐酸米多君(MID)的新有效方法。该方法基于一次性铅笔电极(PE)和玻碳电极(GCE)支持的MID的电氧化。使用循环伏安法、差分脉冲伏安法(DPV)和方波伏安法(SWV)技术进行分析。根据ICH指南对所提出的分析方法进行了验证。在PE上,MID在1.15 - 6.55和0.58 - 3.05 μg mL/mLmL浓度范围内依次进行测定。此外,对于DPV和SWV方法,在GCE上,MID分别在1.15 - 5.28和2.86 - 27.6 μg/mL浓度范围内依次进行测定。所提出的方法成功用于其剂型和人尿中MID的分析,对于DPV和SWV方法,在PE上回收率分别为99.66 ± 0.33、99.8 ± 0.45,在GCE上回收率分别为99.8 ± 0.25、98.7 ± 1.27。所建议的方法可应用于质量控制实验室以及其药代动力学研究中的所研究药物。

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