首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Simultaneous Determination and Validation of Enalapril Maleate, Hydrochlorothiazide and Paracetamol in Combined Tablet Dosage Form Using RP-HPLC Method
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Simultaneous Determination and Validation of Enalapril Maleate, Hydrochlorothiazide and Paracetamol in Combined Tablet Dosage Form Using RP-HPLC Method

机译:RP-HPLC法同时测定片剂中马来酸依那普利,氢氯噻嗪和扑热息痛的同时含量并进行验证

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摘要

A simple, accurate and precise RP-HPLC method has been developed for the simultaneous estimation of enalapril maleate, paracetamol and hydrochlorothiazide in commercially available tablet formulations. The chromatographic separation was achieved on Luna Cg column using mobile phase acetonitrile-phosphate buffentriethylamine (20:79.1:0.1 % v/v/v) (pH 4 ± 0.1) as mobile phase at a flow rate of 1.0 mL/min. Quantitation was carried out at λ_(max) of 215,245 and 270 nm for enalapril maleate, paracetamol and hydrochlorothiazide, respectively. The method was validated as per ICH guidelines. The method may be applied for the routine simultaneous estimation of the above mentioned drugs in tablet dosage form.
机译:已经开发了一种简单,准确和精确的RP-HPLC方法,用于同时估算市售片剂中的马来酸依那普利,扑热息痛和氢氯噻嗪。在Luna Cg柱上进行色谱分离,使用流动相乙腈-磷酸布芬三乙胺(20:79.1:0.1%v / v / v)(pH 4±0.1)作为流动相,流速为1.0 mL / min。在马来酸依那普利,对乙酰氨基酚和氢氯噻嗪的λ_(最大)分别为215,245和270 nm处进行定量。该方法已按照ICH指南进行了验证。该方法可以应用于片剂剂型中上述药物的常规同时估计。

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