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A validated stability indicating HPTLC method for determination of nitazoxanide

机译:经验证的稳定性表明HPTLC方法用于测定硝唑尼特

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A simple, selective, precise and stability-indicating high-performance thin-layer chromatographic (HPTLC) method for nitazoxanide in bulk drug and in formulations was developed and validated. Method employed TLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. Solvent system consisted of ethyl acetate-toluene- methanol (4:6:1, v/v/v). Nitazoxanide was subjected to hydrolysis, oxidation, photolysis and thermal decomposition to establish a validated stability-indicating HPTLC method. Extensive degradation occurred in alkaline medium and in oxidative stress condition and degradation product was well separated from pure drug. Densitometric analysis of nitazoxanide was carried out in absorbance mode at 350 nm. Linear regression analysis data for mean calibration plots showed good linear relationship with r~2 = 0.9997 in 400-1600 ng per spot. Method was validated with respect to linearity, precision, accuracy, specificity and robustness. The limits of detection and quantitation were 15 and 50 ng per spot, respectively. HPTLC method could effectively separate drug from its degradation product and can be employed as a stability-indicating method.
机译:开发并验证了简单的,选择性的,精确的和指示稳定性的高性能薄层色谱法(HPTLC),用于批量药物和制剂中的硝唑尼特。方法采用预涂硅胶60F-254的TLC铝板作为固定相。溶剂体系由乙酸乙酯-甲苯-甲醇(4:6:1,v / v / v)组成。硝唑氧胺经过水解,氧化,光解和热分解,建立了经过验证的表明稳定性的HPTLC方法。在碱性介质和氧化应激条件下发生了广泛的降解,降解产物与纯药物充分分离。硝唑尼特的光密度分析在350 nm的吸收模式下进行。平均校准图的线性回归分析数据显示良好的线性关系,r〜2 = 0.9997,每点400-1600 ng。方法在线性,精度,准确性,特异性和鲁棒性方面得到了验证。每个斑点的检测和定量限分别为15和50 ng。 HPTLC方法可以有效地从降解产物中分离出药物,可以用作稳定性指示方法。

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