I. Alsarra , M. Al-Omar , E.A. Gadkariem , F. Belal
{"title":"Voltammetric determination of montelukast sodium in dosage forms and human plasma","authors":"I. Alsarra , M. Al-Omar , E.A. Gadkariem , F. Belal","doi":"10.1016/j.farmac.2005.04.004","DOIUrl":null,"url":null,"abstract":"<div><p>The voltammetric behaviour of montelukast (MKST) was studied using cyclic voltammetry, direct current (DC<sub>t</sub>), differential pulse polarography (DPP) and alternating current (AC<sub>t</sub>) polarography. MKST exhibited well-defined cathodic waves over the range pH range 1–5. No anodic waves were produced over the same pH range. At pH 1, the analytical pH; the diffusion current constant (Id) was 2.2<!--> <!-->±<!--> <!-->0.01 μA l mmol<sup>–1</sup>. The current concentration plot was rectilinear over the range 2–20 μg ml<sup>–1</sup> with correlation coefficient (<em>n</em> <!-->=<!--> <!-->10) of 0.9943. The lower limit of detection (<em>S</em>/<em>N</em> = 2) was 0.2 μg ml<sup>–1</sup> (3.41<!--> <!-->×<!--> <!-->10<sup>–7</sup> M). The wave has been characterised as being diffusion-controlled, although adsorption phenomenon played a limited role in the electrode reaction. The proposed method was successfully applied to the determination of MKST in commercial tablets, and results were in agreement with those given with a reference HPLC method. The method was further extended to the in vitro determination of the drug in spiked human plasma. The mean % recovery (<em>n</em> <!-->=<!--> <!-->5) was 101.38<!--> <!-->±<!--> <!-->3.85. The number of electrons transferred in the reduction process could be accomplished and a proposal of the electrode reaction was proposed.</p></div>","PeriodicalId":77128,"journal":{"name":"Farmaco (Societa chimica italiana : 1989)","volume":"60 6","pages":"Pages 563-567"},"PeriodicalIF":0.0000,"publicationDate":"2005-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.farmac.2005.04.004","citationCount":"44","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Farmaco (Societa chimica italiana : 1989)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014827X05000844","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 44
Abstract
The voltammetric behaviour of montelukast (MKST) was studied using cyclic voltammetry, direct current (DCt), differential pulse polarography (DPP) and alternating current (ACt) polarography. MKST exhibited well-defined cathodic waves over the range pH range 1–5. No anodic waves were produced over the same pH range. At pH 1, the analytical pH; the diffusion current constant (Id) was 2.2 ± 0.01 μA l mmol–1. The current concentration plot was rectilinear over the range 2–20 μg ml–1 with correlation coefficient (n = 10) of 0.9943. The lower limit of detection (S/N = 2) was 0.2 μg ml–1 (3.41 × 10–7 M). The wave has been characterised as being diffusion-controlled, although adsorption phenomenon played a limited role in the electrode reaction. The proposed method was successfully applied to the determination of MKST in commercial tablets, and results were in agreement with those given with a reference HPLC method. The method was further extended to the in vitro determination of the drug in spiked human plasma. The mean % recovery (n = 5) was 101.38 ± 3.85. The number of electrons transferred in the reduction process could be accomplished and a proposal of the electrode reaction was proposed.