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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Triiodide ion and alizarin red S as two new reagents for the determination of clotrimazole and ketoconazole.
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Triiodide ion and alizarin red S as two new reagents for the determination of clotrimazole and ketoconazole.

机译:三碘离子和茜素红S作为测定克霉唑和酮康唑的两种新试剂。

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摘要

The reactions of a triiodide ion and alizarin red S with two important antifungal drugs containing an imidazole ring (ketoconazole (KC) and clotrimazole (CT)) have been studied for the development of two simple, rapid, sensitive and accurate indirect titrimetric and extractive-spectrophotometric methods for determining the concentration of these drugs. Spectroscopic studies and chemical analysis showed that the protonated forms of KC and CT react with triiodide ion forming highly stable and insoluble ion-pair products such as (KCH(2))(I(3))(2) and (CTH)I(3). Formation of ion-association complexes have been applied to the development of an indirect visual titrimetric method for the determination of KC and CT over the range 10(-5)-10(-2) M. The extractive-spectrophotometric method is based on the formation of (1:1) ion-association complexes between drugs and alizarin red S as chromogenic reagent in acidic citrate buffer that are extractable into chloroform with an absorption maximum at 425 nm. The systemobeyed Beer's law in the concentration range 2.5-50 and 2.7-80 microgram ml(-1) for CT and KC, respectively. The proposed methods were applied for the analysis of the studied drugs in pure forms and their commercial preparations. Results are in good agreement with those obtained by official methods.
机译:研究了三碘离子和茜素红S与两种重要的含咪唑环的重要抗真菌药物(酮康唑(KC)和克霉唑(CT))的反应,以开发两种简单,快速,灵敏和准确的间接滴定和萃取-分光光度法测定这些药物的浓度。光谱研究和化学分析表明,KC和CT的质子化形式与三碘化物离子反应形成高度稳定且不溶的离子对产物,例如(KCH(2))(I(3))(2)和(CTH)I( 3)。离子缔合配合物的形成已被用于间接视觉滴定法的开发,该方法用于测定10(-5)-10(-2)M范围内的KC和CT。萃取光度法基于在酸性柠檬酸盐缓冲液中形成显色剂的药物与茜素红S之间形成(1:1)离子缔合复合物,可提取成氯仿,在425 nm处具有最大吸收。系统遵守比尔定律的CT和KC浓度范围分别为2.5-50和2.7-80微克ml(-1)。所提出的方法被用于分析纯药物及其商业制剂的研究药物。结果与通过官方方法获得的结果非常吻合。

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