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A Validated RP-HPLC Method for the Estimation of Quetiapine in Bulk and Pharmaceutical Formulations

机译:一种验证的RP-HPLC方法,用于批量和药物制剂中喹硫胺的估算

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摘要

A new, simple, specific, sensitive, rapid, accurate and precise RP-HPLC method was developed for the estimation of quetiapine in bulk and pharmaceutical formulations. Quetiapine was chromatographed on a reverse phase C18 Waters column (75x4.6 mm I.D., particle size 3.5 μm) in a mobile phase consisting of phosphate buffer (pH 3.0 adjusted with orthophosphoric acid) and acetonitrile in the ratio 40:60 v/v. The mobile phase was pumped at a flow rate of 0.8 mL/min with detection at 291 nm. The detector response was linear in the concentration of 20-120 μg/mL. The limit of detection and limit of quantitation was found to be 0.2 and 0.75 μg/mL, respectively. The intra and inter day variation was found to be less than 1%. The mean recovery of the drug from the solution was 99%. The proposed method is simple, fast, accurate, precise and reproducible hence, it can be applied for routine quality control analysis of quetiapine in bulk and pharmaceutical formulations.
机译:开发了一种新的,简单,特异性,敏感,快速,准确,精确的RP-HPLC方法,用于估计鳞上和药物制剂中的喹硫氨烯。在具有磷酸盐缓冲液(用正磷酸的pH 3.0调节的pH 3.0)和乙腈中的流动相中,在逆相C18水柱(75×4.6mm I.D.,粒度3.5μm)上进行色谱分离,其比例为40:60V / v。流动相以0.8ml / min的流速泵送,检测为291nm。检测器响应在浓度为20-120μg/ ml的浓度。发现检测极限和定量限制分别为0.2和0.75μg/ ml。发现内部和白天帧内变化小于1%。来自溶液中药物的平均回收率为99%。所提出的方法简单,快速,准确,精确,可再现,可以应用于批量和药物制剂中喹硫胺的常规质量控制分析。

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