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采用曙红用于检测甲苯咪唑的绿色光谱测定法。

Use of eosin for green spectroscopic determination of mebendazole.

机构信息

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.

出版信息

Luminescence. 2020 Aug;35(5):788-796. doi: 10.1002/bio.3785. Epub 2020 Feb 5.

Abstract

New, sensitive, and reliable spectroscopic methods were constructed for the fast determination of the anthelmintic drug mebendazole. The methods depended on the reaction of the amino group in mebendazole with eosin in acidic medium forming an ion pair complex. The first method, Method I, relied on quenching of the native fluorescence of eosin after reaction with mebendazole at pH 3.7 using acetate buffer. Fluorescence quenching was measured at 538 nm after excitation at 518 nm. This method showed a linear response over the concentration range 5.0-20.0 μg/ml. The second method, Method II, was based on measuring the absorbance of the formed complex at 554 nm; the method showed good linearity from 7.0 to 22.0 μg/ml. Different parameters that influenced the formation of the reaction product were carefully investigated to reach the optimized conditions. A comparison between the proposed methods and a previous spectrophotometric method was carried out and there was no significant difference between them. The methods could be applied successfully to determine mebendazole in its tablet form. Moreover, the methods used water as diluting solvent, which made them compatible with the 'green' analytical chemistry principles. No organic solvents were used throughout the study.

摘要

建立了新的、灵敏的和可靠的光谱方法,用于快速测定驱虫药甲苯咪唑。这些方法依赖于甲苯咪唑的氨基与酸性介质中的曙红反应形成离子对复合物。第一种方法,方法 I,依赖于在 pH 3.7 下用乙酸盐缓冲液与甲苯咪唑反应后,曙红的本征荧光猝灭。在 518nm 激发下,在 538nm 处测量荧光猝灭。该方法在 5.0-20.0μg/ml 的浓度范围内呈现线性响应。第二种方法,方法 II,基于测量形成的复合物在 554nm 处的吸光度;该方法在 7.0-22.0μg/ml 范围内表现出良好的线性关系。仔细研究了影响反应产物形成的不同参数,以达到最佳条件。对提出的方法与先前的分光光度法进行了比较,它们之间没有显著差异。这些方法可成功地用于测定其片剂形式的甲苯咪唑。此外,这些方法使用水作为稀释溶剂,这使它们与“绿色”分析化学原理兼容。在整个研究过程中没有使用有机溶剂。

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