气相色谱-火焰离子化检测器(GC-FID)同时测定外用制剂中一般有效成分。

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Anna Ioutsi, Anastasia Sarnitskaya, Mikhail Sumtsov
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引用次数: 0

摘要

建立了一种简单、快速、准确、灵敏的气相色谱法测定外用制剂中樟脑、l -薄荷醇、水杨酸甲酯、水杨酸甲酯、烟酸苄酯和非乙酰胺的含量。说明了用一种分析方法测定低沸点成分和高沸点成分的可能性。通过对大量色谱参数和样品制备阶段的影响进行评价,对该方法进行了优化。它是根据国际协调理事会的准则进行验证的。烟酸苄酯和l -薄荷醇的定量限为0.7 μg/mL,水杨酸的定量限为41 μg/mL。该方法重复性高,回收率好。该方法在软膏和乳膏中的实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous Determination of General Active Ingredients in Topical Formulations by Gas Chromatography with Flame Ionization Detection (GC-FID).

A simple, fast, precision and sensitive gas chromatographic method was developed for determination of camphor, L-menthol, methyl salicylate, salicylic acid, benzyl nicotinate and nonivamide in topical formulations. The possibility of determination low-boiling components and high-boiling components by a single analytical method was shown. The method was optimized by evaluating the effect of a large number of chromatographic parameters and sample preparation stages. It was validated according to the International Council on Harmonization guidelines. Limit of quantification of active components were achieved from 0.7 μg/mL for benzyl nicotinate and L-menthol to 41 μg/mL for salicylic acid. High repeatability and good recovery values were demonstrated. The practical application of the proposed method was shown for ointments and cream.

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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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