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采用原子吸收光谱法和比色法测定某些抗组胺药物。

Determination of some antihistaminic drugs by atomic absorption spectrometry and colorimetric methods.

作者信息

El-Kousy N, Bebawy L I

机构信息

National Organization for Drug Control and Research, Dokki, Giza, Egypt.

出版信息

J Pharm Biomed Anal. 1999 Aug;20(4):671-9. doi: 10.1016/s0731-7085(99)00040-0.

Abstract

Atomic absorption spectrometry (AAS) and colourimetric methods have been developed for the determination of pizotifen (I), ketotifen (II) and loratadine (III). The first method depends on the reaction of the three drugs (I); (II) and (III) with cobalt thiocyanate reagent at pH 2 to give ternary complexes. These complexes are readily extracted with organic solvent and estimated by indirect atomic absorption method via the determination of the cobalt content in the formed complex after extraction in 0.1 M hydrochloric acid. It was found that the three drugs can be determined in the concentration ranges from 10 to 74, 12 to 95 and 10 to 93 microg ml(-1) with mean percentage recovery of 99.71+/-0.87, 99.70+/-0.79 and 99.62+/-0.75%, respectively. The second method is based on the formation of orange red ion pairs as a result of the reaction between (I); (II) and (III) and molybdenum thiocyanate with maximum absorption at 469.5 nm in dichloromethane. Appropriate conditions were established for the colour reaction. Under the proposed conditions linearity was obeyed in the concentration ranges 3.5-25, 5-37.5 and 2.5-22.5 microg ml(-1) with mean percentage recovery of 99.60+/-0.41, 100.11+/-0.43 and 99.31+/-0.47% for (I): (II) and (III), respectively. The third method depends on the formation of radical ion using 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ). The colour formed was measured at 588 nm for the three drugs (I); (II) and (III), respectively. The method is valid in concentration range 10-80 microg ml(-1) with mean percentage recovery 99.75+/-0.44, 99.94+/-0.72 and 99.17+/-0.36% for (I); (II) and (III), respectively. The proposed methods were applied to the analysis of pharmaceutical preparations. The results obtained were statistically analysed and compared with those obtained by applying the official and reference methods.

摘要

已开发出原子吸收光谱法(AAS)和比色法用于测定匹莫齐特(I)、酮替芬(II)和氯雷他定(III)。第一种方法基于三种药物(I)、(II)和(III)在pH 2条件下与硫氰酸钴试剂反应生成三元络合物。这些络合物很容易用有机溶剂萃取,并通过在0.1 M盐酸中萃取后测定形成的络合物中的钴含量,采用间接原子吸收法进行估算。结果发现,三种药物的测定浓度范围分别为10至74、12至95和10至93 μg/ml,平均回收率分别为99.71±0.87%、99.70±0.79%和99.62±0.75%。第二种方法基于(I)、(II)和(III)与硫氰酸钼反应形成橙红色离子对,在二氯甲烷中于469.5 nm处有最大吸收。建立了显色反应的适宜条件。在所提出的条件下,(I)、(II)和(III)在浓度范围3.5 - 25、5 - 37.5和2.5 - 22.5 μg/ml内呈线性关系,平均回收率分别为99.60±0.41%、100.11±0.43%和99.31±0.47%。第三种方法基于使用2,3 - 二氯 - 5,6 - 二氰基 - 对苯醌(DDQ)形成自由基离子。分别在588 nm处测定三种药物(I)、(II)和(III)形成的颜色。该方法在浓度范围10 - 80 μg/ml内有效,(I)、(II)和(III)的平均回收率分别为99.75±0.44%、99.94±0.72%和99.17±0.36%。所提出的方法应用于药物制剂的分析。对所得结果进行了统计分析,并与采用官方方法和参考方法所得结果进行了比较。

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