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 >Determination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LC.
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Determination of theophylline and ephedrine HCL in tablets by ratio-spectra derivative spectrophotometry and LC.

机译:比率光谱导数分光光度法和液相色谱法测定片剂中茶碱和麻黄碱的含量

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摘要

Two methods are described for the determination of theophylline (THP) and ephedrine hydrochloride (EPH) in combined pharmaceutical tablet forms. The first method depends on the use of the first derivative of the ratio-spectra obtained by dividing the absorption spectrum of binary mixtures by a standard spectrum of one of the compounds. The first derivative amplitudes at 231.8 and 250.3 nm were selected for the assay of THP and EPH, respectively. Calibration graphs were established for 20-180 microg ml(-1) for THP and 10-50 microg ml(-1) for EPH. The second method is based on high-performance liquid chromatography on a reversed-phase column using a mobile phase of methanol-water (40+60,v/v) (pH 3) with detection at 217 nm. Linearity was obtained in the concentration range of 5-150 microg ml(-1) for THP and 15-75 microg ml(-1) for EPH. The detection limits for THP and EPH were 0.73 and 0.92 microg ml(-1) by ratio-spectra derivative spectrophotometry and 0.59 and 0.86 microg ml(-1) by HPLC, respectively. The proposed methods were successfully applied to the determination of these drugs in laboratory-prepared mixtures and in tablets. The relative standard deviations were found to be less than 1.5%, indicating reasonable repeatibility of both methods.
机译:描述了两种用于测定组合药物片剂中茶碱(THP)和盐酸麻黄碱(EPH)的方法。第一种方法取决于使用比率光谱的一阶导数,该比率光谱是通过将二元混合物的吸收光谱除以一种化合物的标准光谱获得的。选择THP和EPH分别在231.8和250.3 nm处的一阶导数幅度。建立了THP的20-180 microg ml(-1)和EPH的10-50 microg ml(-1)的校正图。第二种方法基于反相色谱柱上的高效液相色谱,使用甲醇-水(40 + 60,v / v)(pH 3)的流动相,并在217 nm处检测。对于THP,对于EPH,在15-75 microg ml(-1)的浓度范围内获得线性度。通过比率-光谱导数分光光度法测定的THP和EPH的检出限分别为0.73和0.92 microg ml(-1),通过HPLC的检出限分别为0.59和0.86 microg ml(-1)。所提出的方法已成功应用于实验室制备的混合物和片剂中这些药物的测定。发现相对标准偏差小于1.5%,表明两种方法均具有合理的重复性。

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