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A Simple RP-HPLC Method for Quantitation of Itopride HCl in Tablet Dosage Form

机译:片剂剂型中盐酸依托必利的简单RP-HPLC方法

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摘要

An isocratic reversed phase high-performance liquid chromatographic method with ultraviolet detection at 220 nm has been developed for the quantification of itopride hydrochloride in tablet dosage form. The quantification was carried out using C8 column (250 mm × 4.6 mm), 5-μm particle size SS column. The mobile phase comprised of two solvents (Solvent A: buffer 1.4 mL ortho-phosphoric acid adjusted to pH 3.0 with triethyl amine and Solvent B: acetonitrile). The ratio of Solvent A: Solvent B was 75:25 v/v. The flow rate was 1.0 mL -1with UV detection at 220 nm. The method has been validated and proved to be robust. The calibration curve was linear in the concentration range of 80-120% with coefficient of correlation 0.9995. The percentage recovery for itopride HCl was 100.01%. The proposed method was validated for its selectivity, linearity, accuracy, and precision. The method was found to be suitable for the quality control of itopride HCl in tablet dosage formulation.
机译:已经开发了等度反相高效液相色谱法,该方法在220 nm处具有紫外线检测功能,用于定量片剂剂型中盐酸伊托必利。使用C8色谱柱(250 mm×4.6 mm),5-μm粒径SS色谱柱进行定量。流动相由两种溶剂组成(溶剂A:缓冲液1.4 mL正磷酸,用三乙胺调节至pH 3.0,溶剂B:乙腈)。溶剂A∶溶剂B的比例为75∶25v / v。流速为1.0 mL -1 ,在220 nm处进行UV检测。该方法已经过验证并证明是可靠的。校正曲线在80-120%的浓度范围内呈线性,相关系数为0.9995。盐酸伊托必利的回收率为100.01%。该方法的选择性,线性,准确性和精密度均得到验证。发现该方法适用于片剂剂量制剂中盐酸伊托必利的质量控制。

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