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Determination of astemizole in pharmaceutical preparations using spectrophotometric methods.

机译:分光光度法测定药物制剂中的阿司咪唑。

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摘要

UV absorption and second derivative spectrophotometric methods were developed for the determination of astemizole in commercial pharmaceutical formulations containing this compound alone. Solutions of astemizole in 0.1 M HCl:methanol (1:3) were used in the methods and the linearity range was 4.6-45.8 microg ml(-1) in both methods. The mean recoveries and relative standard deviations were calculated and the method was applied to two commercial preparations marketed in Turkey. Results were compared with the literature method, HPLC. Also, two new spectrophotometric methods are described for the simultaneous determination of astemizole and pseudoephedrine hydrochloride in their combination. In the first method, first derivative spectrophotometry, dA/dlambda values were read at selected wavelengths in zero-crossing points in the first derivative spectra of the mixture solution in 0.1 M HCl:methanol (1:3). In the second, ratio spectra derivative spectrophotometry, analytical signals were measured at the wavelengths corresponding to either maximums and minimums for both drugs in their solution in 0.1 M HCl:methanol (1:3) in the first derivative spectra of their ratio spectra. The procedures do not require any separation step. The mean recoveries were found satisfactory in the methods.
机译:开发了紫外吸收和二阶导数分光光度法,用于测定仅含有该化合物的商业药物制剂中的阿斯咪唑。该方法使用阿司咪唑在0.1 M HCl:甲醇(1:3)中的溶液,两种方法的线性范围均为4.6-45.8 microg ml(-1)。计算平均回收率和相对标准偏差,并将该方法应用于在土耳其销售的两种商业制剂。将结果与文献方法HPLC进行比较。此外,描述了两种新的分光光度法,用于同时测定阿司咪唑和盐酸伪麻黄碱的组合。在第一种方法中,在一阶导数分光光度法中,在0.1 M HCl:甲醇(1:3)的混合溶液的一阶导数光谱中的零交叉点的选定波长处读取dA / dlambda值。在第二种比率光谱导数分光光度法中,在对应比率光谱的一阶导数光谱中,在与两种药物在0.1 M HCl:甲醇(1:3)溶液中的最大值和最小值相对应的波长下测量分析信号。该过程不需要任何分离步骤。方法中的平均回收率令人满意。

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