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首页> 外文期刊>Asian journal of research in chemistry >Development and Method Validation of RP-HPLC For Simultaneous Determination of Pregabalin and Methylcobalamin in Pure and Pharmaceutical Dosage Form
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Development and Method Validation of RP-HPLC For Simultaneous Determination of Pregabalin and Methylcobalamin in Pure and Pharmaceutical Dosage Form

机译:RP-HPLC同时测定纯和药物剂型中Praetabalin和甲基钴素的开发和方法验证

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摘要

To develop a simple, sensitive, precise and accurate RP-HPLC method was developed for the quantitative estimation of Pregabalin and Methylcobalamin in bulk drug and the most common from delivery of drugs oral, sublingual, injection pharmaceutical dosage forms. This method was Pregabalin and Methylcobalamin was freely soluble in ethanol, methanol and sparingly soluble in water. The %RSD values were within 2 and the method was found to be precise. The results expressed in Tables for RP-HPLC method was promising. The RP-HPLC method is more sensitive, accurate and precise compared to the Spectrophotometric methods. This method can be used for the routine determination of Pregabalin and Methylcobalamin in bulk drug and in Pharmaceutical dosage forms.
机译:为了开发简单,敏感,精确和准确的RP-HPLC方法是开发的,用于散装药中普瑞巴林和甲基丙氨酸的定量估计,最常见的药物口服,舌下,注射药物剂型。 该方法是普瑞巴林,并且甲基钴胺在乙醇中可自由溶于乙醇,甲醇并省略地溶于水。 %RSD值在2内,发现该方法精确。 在RP-HPLC方法表中表达的结果是有前途的。 与分光光度法相比,RP-HPLC方法更敏感,准确和精确。 该方法可用于常规测定散装药物和药物剂型中普瑞巴林和甲基钴胺。

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