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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Fluorimetric and spectrophotometric determination of ritodrine hydrochloride in bulk and pharmaceutical formulations.
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Fluorimetric and spectrophotometric determination of ritodrine hydrochloride in bulk and pharmaceutical formulations.

机译:荧光和分光光度法测定散装和药物制剂中盐酸利托君的含量。

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摘要

Two simple sensitive and accurate methods have been developed for the determination of ritodrine hydrochloride in bulk and pharmaceutical preparations. The first method involves the direct measurement of the native fluorescence of the drug in the concentration range 4-9 microg ml(-1), the second method is based on the oxidation of ritodrine HCl with cerium(IV) followed either by spectrophotometric or fluorimetric measurement in the concentration ranges 0.5-1.0 and 0.05-0.1 microg ml(-1), respectively. The interference of various formulation excipients was examined. The reliability of the proposed methods was checked at three different concentrations; the standard deviation varied from 2.7 x 10(-3)-0.109. The described methods have been applied to the determination of ritodrine HCl in tablets and ampoules. The assay results showed insignificant difference with those of the official USP 23 HPLC method.
机译:已经开发了两种简单,灵敏,准确的方法来测定散装和药物制剂中的盐酸利多君。第一种方法涉及直接测量浓度范围为4-9 microg ml(-1)的药物的天然荧光,第二种方法是基于盐酸ritritrine HCl与铈(IV)的氧化,然后采用分光光度法或荧光法浓度范围分别为0.5-1.0和0.05-0.1 microg ml(-1)。检查了各种制剂赋形剂的干扰。在三种不同浓度下检查了所提出方法的可靠性。标准偏差为2.7 x 10(-3)-0.109。所描述的方法已经应用于片剂和安瓿瓶中盐酸利托君的测定。测定结果显示与官方的USP 23 HPLC方法无明显差异。

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