A. Ioutsi, M. Sumtsov, D. A. Artyushenko, D. Bychenkov, A. N. Blinov
{"title":"毛细管气液色谱法测定对羟基苯甲酸酯在药物分析中的适用性","authors":"A. Ioutsi, M. Sumtsov, D. A. Artyushenko, D. Bychenkov, A. N. Blinov","doi":"10.30895/1991-2919-2019-9-2-123-130","DOIUrl":null,"url":null,"abstract":"The traditional gas-liquid chromatography (GLC) method using packed columns is still used in pharmaceutical analysis for determination of parabens, despite the fact that this technique has a number of serious drawbacks.The aim of the study was to develop a more effective capillary GLC method for determination of parabens in active pharmaceutical ingredients and finished pharmaceutical products.Materials and methods: the study was performed using Agilent 6890N and Agilent 7890B systems with flame-ionisation detectors. The systems were equipped with Agilent 7683B and Agilent G4513A autosamplers, respectively. The following columns were used in the study: ZB-1 15 m х 0.32 mm х 0.25 pm, DB-1 30 m х 0.32 mm х 3.0 pm, Cp-Sil 5-CB 30 m х 0.32 mm х 3.0 pm.Results: the authors developed a method for methylparaben and propylparaben determination using capillary column GLC. The chromatographic parameters (chromatographic system performance, reproducibility of peak areas, peak asymmetry) were determined for both capillary and packed column GLC. The authors outlined the prospects for simultaneous determination of several compounds using the proposed method: a four-component mixture containing methyl-, ethyl-, propyl-, and butylparaben was separated in 9 minutes. The authors used Loma Lux Psoriasis to perform partial validation of the test method. They determined the linearity range and the limit of quantitation for methylparaben and propylparaben, and verified accuracy and intermediate precision of the test method.Conclusions: the results of the study allowed for selection of optimal chromatographic conditions for rapid and high-precision determination of methylparaben and propylparaben in medicinal products. The developed method is recommended for control of the content of these compounds in medicinal products.","PeriodicalId":22286,"journal":{"name":"The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products","volume":"91 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Applicability of Capillary Gas-Liquid Chromatography for Determination of Parabens in Pharmaceutical Analysis\",\"authors\":\"A. Ioutsi, M. Sumtsov, D. A. Artyushenko, D. 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引用次数: 2
摘要
传统的填充柱气液色谱法(GLC)在药物分析中仍被用于对羟基苯甲酸酯的测定,尽管这种技术有许多严重的缺点。本研究的目的是建立一种更有效的毛细管气相色谱法测定药物活性成分和成品中对羟基苯甲酸酯的含量。材料和方法:本研究使用带有火焰电离检测器的Agilent 6890N和Agilent 7890B系统进行。系统分别配备Agilent 7683B和Agilent G4513A自动进样器。所用色谱柱为:ZB-1 15 m, 0.32 mm, 0.25 pm; DB-1 30 m, 0.32 mm, 3.0 pm; Cp-Sil - 5-CB, 30 m, 0.32 mm, 3.0 pm。结果:建立了毛细管色谱法测定对羟基苯甲酸甲酯和对羟基苯甲酸丙酯的方法。测定了毛细管色谱和填充柱色谱的色谱参数(色谱系统性能、峰面积重现性、峰不对称性)。作者概述了使用该方法同时测定几种化合物的前景:在9分钟内分离出含有甲基,乙基,丙基和对羟基苯甲酸丁酯的四组分混合物。作者使用Loma Lux牛皮癣对测试方法进行部分验证。确定了对羟基苯甲酸甲酯和对羟基苯甲酸丙酯的线性范围和定量限,验证了测试方法的准确度和中间精密度。结论:研究结果为快速、高精度测定药品中对羟基苯甲酸甲酯和对羟基苯甲酸丙酯的色谱条件选择提供了依据。建议本方法用于药品中这些化合物的含量控制。
Applicability of Capillary Gas-Liquid Chromatography for Determination of Parabens in Pharmaceutical Analysis
The traditional gas-liquid chromatography (GLC) method using packed columns is still used in pharmaceutical analysis for determination of parabens, despite the fact that this technique has a number of serious drawbacks.The aim of the study was to develop a more effective capillary GLC method for determination of parabens in active pharmaceutical ingredients and finished pharmaceutical products.Materials and methods: the study was performed using Agilent 6890N and Agilent 7890B systems with flame-ionisation detectors. The systems were equipped with Agilent 7683B and Agilent G4513A autosamplers, respectively. The following columns were used in the study: ZB-1 15 m х 0.32 mm х 0.25 pm, DB-1 30 m х 0.32 mm х 3.0 pm, Cp-Sil 5-CB 30 m х 0.32 mm х 3.0 pm.Results: the authors developed a method for methylparaben and propylparaben determination using capillary column GLC. The chromatographic parameters (chromatographic system performance, reproducibility of peak areas, peak asymmetry) were determined for both capillary and packed column GLC. The authors outlined the prospects for simultaneous determination of several compounds using the proposed method: a four-component mixture containing methyl-, ethyl-, propyl-, and butylparaben was separated in 9 minutes. The authors used Loma Lux Psoriasis to perform partial validation of the test method. They determined the linearity range and the limit of quantitation for methylparaben and propylparaben, and verified accuracy and intermediate precision of the test method.Conclusions: the results of the study allowed for selection of optimal chromatographic conditions for rapid and high-precision determination of methylparaben and propylparaben in medicinal products. The developed method is recommended for control of the content of these compounds in medicinal products.