首页> 外文期刊>Journal of the Iranian Chemical Society >Development and Validation of RP-HPLC Method for Simultaneous Determination of Glipizide, Rosiglitazone, Pioglitazone, Glibenclamide and Glimepiride in Pharmaceutical Dosage Forms and Human Plasma
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Development and Validation of RP-HPLC Method for Simultaneous Determination of Glipizide, Rosiglitazone, Pioglitazone, Glibenclamide and Glimepiride in Pharmaceutical Dosage Forms and Human Plasma

机译:RP-HPLC法同时测定药物剂型和人血浆中格列吡嗪,罗格列酮,吡格列酮,格列本脲和格列美脲的开发和验证

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摘要

A simple, high performance liquid chromatographic method has been developed for the simultaneous determination of glipizide, rosiglitazone, pioglitazone, glibenclamide and glimepiride in pharmaceutical dosage forms and human plasma. The elution was performed using a mobile phase mixture of 0.05% Triethylamine (pH-3.5, adjusted with ortho phosphoric acid), acetonitrile and methanol in the ratio of 55:15:30 at a flow rate of 1 ml min~(-1) on a phenomenex C_(18) column (150 × 4.6 mm, i.d., 5 μm) at ambient temperature. The drugs were monitored at a wavelength of 248 nm and were separated within 20 min. Mixtures of formulations were prepared in suitable dilutions and plasma samples were prepared by extraction with acetonitrile. The method was successful in detecting the drugs at a concentration of less than 0.1 μg ml~(-1) for each drug and %RSD for intra- and inter-day studies was found to be less than 4.34 for all the selected concentrations. Moreover, the method was validated as per ICH guidelines and the results were found to be within the acceptable range. Hence, the proposed method can be used for the routine quality control of the drugs and can also be applied to pharmacokinetic studies.
机译:已经开发了一种简单的高效液相色谱方法,用于同时测定药物剂型和人血浆中的格列吡嗪,罗格列酮,吡格列酮,格列本脲和格列美脲。使用0.05%三乙胺(pH-3.5,用正磷酸调节),乙腈和甲醇的流动相混合物以55:15:30的比例以1 ml min〜(-1)的流速进行洗脱在室温下在phenomenex C_(18)色谱柱(150×4.6 mm,内径,5μm)上在248 nm的波长处监测药物,并在20分钟内分离。以合适的稀释度制备制剂的混合物,并通过用乙腈萃取来制备血浆样品。该方法成功地检测出每种药物的浓度均小于0.1μgml〜(-1),并且日间和日间研究的%RSD对于所有选定浓度均小于4.34。此外,该方法已按照ICH指南进行了验证,结果在可接受范围内。因此,所提出的方法可以用于药物的常规质量控制,也可以用于药代动力学研究。

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