首页> 外文期刊>Acta Chimica and Pharmaceutica Indica >A Pre-Column Derivatization Technique for The Development and Validation of a HPLC-UV Method for the Determination of Amantadine Hydrochloride in Bulk and Formulations by using (2-Napthoxy) Acetyl Chloride
【24h】

A Pre-Column Derivatization Technique for The Development and Validation of a HPLC-UV Method for the Determination of Amantadine Hydrochloride in Bulk and Formulations by using (2-Napthoxy) Acetyl Chloride

机译:柱前衍生技术用于开发和验证高效液相色谱-紫外法测定(2-萘氧基)乙酰氯测定散装和制剂中盐酸金刚烷胺的含量

获取原文
           

摘要

A simple, precise, and accurate HPLC method has been developed and validated for the quantitative analysis of amantadine hydrochloride in tablet form by using (2-Napthoxy) Acetyl chloride as derivatization agent and memantine as an internal standard. An isocratic separation was achieved using inertsil ODS-3V, 250 x 4.6, 5 μm column with a flow rate of 1.5 mL/min and UV detector at 226 nm. The mobile phase consisted of 0.02 M ammonium acetate buffer and methanol in the ratio (12:88). The retention time for Amantadine and Memantine was around 6.23 and 8.62. The method was validated for specificity, linearity, precision, accuracy, robustness, and solution stability. The specificity of the method was determined by assessing interference from the placebo. The method was linear over the concentration range 28-171 μg/mL (r2 = 0.999) with a Limit of Detection (LOD) and Limit of Quantitation (LOQ) 0.23 and 0.69 μg/mL, respectively. The accuracy of the method was between 98.9-99.6%. The method was found to be robust and suitable for the quantitative analysis of amantadine hydrochloride in a tablet formulation
机译:通过使用(2-萘氧基)乙酰氯作为衍生剂和美金刚作为内标物,开发了一种简单,精确和准确的HPLC方法,并已用于定量分析片剂中的盐酸金刚烷胺。使用inertsil ODS-3V,250 x 4.6、5μm色谱柱,流速为1.5 mL / min和226 nm的UV检测器可实现等度分离。流动相由0.02 M乙酸铵缓冲液和比例为12:88的甲醇组成。金刚烷胺和美金刚胺的保留时间约为6.23和8.62。验证了该方法的特异性,线性,精密度,准确性,鲁棒性和溶液稳定性。该方法的特异性通过评估安慰剂的干扰来确定。该方法在浓度范围28-171μg/ mL(r2 = 0.999)时呈线性,检测限(LOD)和定量限(LOQ)分别为0.23和0.69μg/ mL。该方法的准确性在98.9-99.6%之间。发现该方法可靠且适用于片剂中盐酸金刚烷胺的定量分析

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号