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首页> 外文期刊>Journal of Surfactants and Detergents >A Micellar Liquid Chromatographic Method for the Determination of Azosemide in Solubilized System
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A Micellar Liquid Chromatographic Method for the Determination of Azosemide in Solubilized System

机译:一种胶束液相色谱法测定溶解体系中的亚沸胺

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摘要

A simple micellar liquid chromatographic method was developed and validated for the determination of azosemide (AZS). The method incorporates surfactant media beyond the critical micellar concentration level for the study of AZS in bulk and pharmaceutical dosage forms. Quantitation was achieved through UV detection. An interpretive optimization procedure was used to ascertain the optimum conditions based on the accurate description of the retention and shape of the chromatographic peak for quantification of AZS, viz., selection of surfactants, pH of buffer solution, concentration of surfactant and selection of solvent etc. The method was successfully validated as per the requirements of the international Council for Harmonisation (ICH) guidelines and showed excellent linearity within the limits of detection and limit of quantitation. The method was linear over the concentration range 0.001-0.2 mg ml(-1) with regression coefficient (r (2)) 0.999. The proposed method was successfully applied for ascertaining the stability and determination of AZS under different stressed conditions viz., basic, acidic, oxidative, photolytic, and thermal degradation. The method elicited good selectivity, repeatability, linearity and sensitivity of the validated parameters. Recoveries obtained were in a range of 98.90-99.58%. The method allows accurate and reliable determination of AZS for drug stability assays in pharmaceutical investigations using environmentally friendly materials.
机译:开发并验证了一种简单的胶束液相色谱法,用于测定亚沸胺(AZ)。该方法包含除了批量和药物剂型中AZ的临界胶束浓度水平之外的表面活性剂培养基。通过UV检测实现定量。用于基于用于量化Azs,ZiZ的色谱峰的保持和形状的准确描述来确定最佳条件,用于定量Azs,Ziz,表面活性剂的选择,缓冲溶液的pH,表面活性剂浓度和溶剂的选择等。根据国际委员会协调理事会(ICH)指南的要求,该方法已成功验证,并在检测和定量限制范围内显示出优异的线性。该方法在浓度范围内与回归系数(R(2))为0.999的浓度范围为0.001-0.2mg ml(-1)。该提出的方法已成功地应用于确定不同应力条件下的AZ的稳定性和测定。,碱性,酸性,氧化,光解性和热降解。该方法引发了验证参数的良好选择性,可重复性,线性度和灵敏度。获得的回收率在98.90-99.58%的范围内。该方法允许使用环保材料的药物调查中的药物稳定性测定的准确可靠测定AZ。

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