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HPTLC METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS DETERMINATION OF RESERPINE AND GALLIC ACID IN AN AYURVEDIC FORMULATION

机译:HPTLC方法的开发和验证在阿育吠陀制剂中同时测定血清和食子酸的验证

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摘要

A simple, precise, accurate, robust HPTLC method was developed and validated for simultaneous estimation of reserpine and gallic acid in an Ayurvedic formulation. The two markers were resolved using TLC plates pre-coated with silica gel 60F_(254) using the mobile phase Toluene: Acetone: Glacial acetic acid in the ratio 4:1:1 V/V with a saturation time of 10 minutes. The R_f values of gallic acid and reserpine were found to be 0.31 ± 0.2 and 0.54 ± 0.2, respectively at 268 nm. Linear response was observed in the concentration range of 20-80 ppm for reserpine and 150-210 ppm for gallic acid, with correlation coefficient (r2) of 0.995 and 0.997 for reserpine and gallic acid respectively. The developed method was applied for the quantitation of markers in a marketed formulation, Cardostab tablet. This method can also be used to evaluate other formulations containing reserpine and gallic acid as the constituents, thus conforming to the need of ensuring quality and safety of polyherbal formulations.
机译:开发并验证了一种简单,精确,准确,鲁棒的HPTLC方法,以便在阿育吠陀制剂中同时估计血清培养物和食小酸。使用使用流动相甲苯预涂有硅胶60F_(254)的TLC板来解决两个标记:丙酮:冰醋酸中的冰醋酸为4:1:1V / v,饱和时间为10分钟。在268nm的情况下,发现无碱酸和血清的R_F值为0.31±0.2和0.54±0.2。在20-80ppm的浓度范围内观察到线性响应,用于预转血剂和150-210ppm,用于无碱,具有0.995和0.997的相关系数(R2)分别用于血红酸和无食酸。施加了开发的方法,用于定量销售配方中标志物,Carkostab片剂。该方法还可用于评估含有转血剂和无碱作为成分的其他制剂,从而符合确保聚丙酯配方的质量和安全性的需求。

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