Estimation of citicoline sodium in tablets by difference spectrophotometric method

S. Panda, Ganeswar Mohanta, B. Kumar
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引用次数: 6

Abstract

Aim: The present work deals with development and validation of a novel, precise, and accurate spectrophotometric method for the estimation of citicoline sodium (CTS) in tablets. This spectrophotometric method is based on the principle that CTS shows two different forms that differs in the absorption spectra in basic and acidic medium. Materials and Methods: The present work was being carried out on Shimadzu 1800 Double Beam UV-visible spectrophotometer. Difference spectra were generated using 10 mm quartz cells over the range of 200-400 nm. Solvents used were 0.1 M NaOH and 0.1 M HCl. Results: The maxima and minima in the difference spectra of CTS were found to be 239 nm and 283 nm, respectively. Amplitude was calculated from the maxima and minima of spectrum. The drug follows linearity in the range of 1-50 μ/ml (R 2 = 0.999). The average % recovery from the tablet formulation was found to be 98.47%. The method was validated as per International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use: ICH Q2(R1) Validation of Analytical Procedures: Text and Methodology guidelines. Conclusion: This method is simple and inexpensive. Hence it can be applied for determination of the drug in pharmaceutical dosage forms.
差示分光光度法测定片剂中胞胆碱钠的含量
目的:建立一种新的、精确的、准确的测定片中胞胆碱钠(CTS)含量的分光光度法。这种分光光度法是基于CTS在碱性和酸性介质中显示两种不同形式的吸收光谱的原理。材料与方法:本工作在岛津1800双光束紫外可见分光光度计上进行。使用10 mm石英电池在200-400 nm范围内生成差分光谱。所用溶剂为0.1 M NaOH和0.1 M HCl。结果:CTS差异光谱的最大值为239 nm,最小值为283 nm。振幅由频谱的最大值和最小值计算。在1 ~ 50 μ/ml范围内呈线性关系(r2 = 0.999)。该片剂的平均回收率为98.47%。该方法按照人用药品注册技术要求国际协调会议:ICH Q2(R1)分析方法验证:文本和方法学指南进行验证。结论:该方法操作简便,成本低廉。因此,可用于药物剂型的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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