Green TLC-Densitometric Method for Simultaneous Determination of Antazoline and Tetryzoline: Application to Pharmaceutical Formulation and Rabbit Aqueous Humor.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Ola G Hussein, Yasmin Rostom, Mohamed Abdelkawy, Mamdouh R Rezk, Dina A Ahmed
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引用次数: 0

Abstract

Ophthalmic pharmaceutical preparation containing antazoline (ANT) and tetryzoline (TET) is prescribed widely as an over the counter medication for allergic conjunctivitis treatment. Development of a selective, simple and environmentally friendly thin-layer chromatographic method established to determine both ANT and TET in their pure forms, pharmaceutical formulation and spiked aqueous humor samples. By using silica gel plates and means of a developing system consists of ethyl acetate:ethanol (5:5, by volume), the studied drugs separation was achieved, and scanning was carried out at 220.0 nm for the separated bands with a 0.2-18.0 μg/band concentration range for each of ANT and TET. Standard addition technique application was carried out to determine the proposed method validity. Statistical comparison was made between the proposed method and the official methods ANT and TET showing no significant difference concerning accuracy and precision. Furthermore, greenness profile assessment was accomplished by means of four metric tools, namely, analytical greenness, green analytical procedure index, analytical eco-scale and national environmental method index.

Highlights.

同时测定安他唑啉和泰特唑啉的绿色 TLC 密度测定法:在药物制剂和家兔水体中的应用
含有安他唑啉(ANT)和泰曲唑啉(TET)的眼科药物制剂被广泛用作治疗过敏性结膜炎的非处方药物。本研究开发了一种选择性强、简便且环保的薄层色谱法,用于测定纯品、药物制剂和加标水样中的 ANT 和 TET。使用硅胶板和由乙酸乙酯:乙醇(体积比为 5:5)组成的显影系统实现了所研究药物的分离,并在 220.0 纳米波长下对分离带进行扫描,ANT 和 TET 的浓度范围分别为 0.2-18.0 μg/带。应用标准添加技术确定了拟议方法的有效性。对拟议方法与官方方法 ANT 和 TET 进行了统计比较,结果表明两者在准确度和精密度方面没有显著差异。此外,还通过四种度量工具(即分析绿色度、绿色分析程序指数、分析生态尺度和国家环境方法指数)对绿色概况进行了评估。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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