Development, Validation, Identification and Estimation of Quinoline Yellow in the Levodopa and Carbidopa Pharmaceutical Combined dosage form by Ultra violet Visible Spectrophotometer

Bhagwan S. Mehetre, Krishnakant T. Waghmode
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Abstract

A simple, cost-effective, précised, accurate and robust Ultra Violet spectrophotometric method [1, 2 ] has been developed for the Identification and estimation of Quinoline Yellow in the Levodopa and Carbidopa tablet dosage forms. It is used as a colourant in the pharmaceutical tablet’s dosage form. UV scan of Quinoline yellow was taken from the entire UV range of 200 to 800 nm. From the spectrum, maximum absorption was observed at 414nm (λmax) for the Quinoline Yellow. Method was found to be specific with no interference due to blank and placebo, The method was linear with a correlation coefficient of more than 0.999, and Accuracy was in the range of 98.3 to 101.3, In the robustness study employed for standard and sample preparation showed no impact on the results, by deliberate changes proves method is robust and can be utilized for regular analysis. Method validation was performed with reference to ICH guidelines Q2R1.
用紫外可见分光光度计开发、验证、鉴定和估算左旋多巴和卡比多巴复方制剂中的喹啉黄
为鉴定和估算左旋多巴和卡比多巴片剂中的喹啉黄,我们开发了一种简单、经济、简便、准确和稳健的紫外分光光度法[1, 2 ]。喹啉黄在药片剂型中用作着色剂。喹啉黄的紫外线扫描范围为 200 至 800 纳米。从光谱中观察到,喹啉黄在 414nm 处有最大吸收(λmax)。该方法线性相关系数大于 0.999,准确度在 98.3 至 101.3 之间,在稳健性研究中,采用的标准和样品制备方法对结果没有影响。方法验证参照 ICH 指南 Q2R1 进行。
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