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用于药物制剂中氯丙嗪含量测定的流动注射分光光度法的顺序优化。

Sequential optimization of a flow injection spectrophotometric method for the assay of chlorpromazine in pharmaceutical preparations.

作者信息

Suliman F E, Sultan S M

机构信息

Chemistry Department, King Fahd University, Dhahran, Saudi Arabia.

出版信息

Talanta. 1994 Nov;41(11):1865-71. doi: 10.1016/0039-9140(94)80193-2.

Abstract

A new simple flow injection spectrophotometric method for the assay of chlorpromazine using cerium(IV) in sulfuric acid media was developed. The oxidized form of the drug was monitored at the maximum absorbance of 526 nm. The optimum conditions were 0.035M sulfuric acid, 3.80 x 10(-3)M cerium(IV), flow rate 4.85 ml/min, coil length 45 cm and sample size 110 mm(3). Optimization was carried out by the modified simplex method. Response surface methodology was employed to investigate the ruggedness of the method. A sampling frequency of 120 hr(-1) was attained. Relative standard deviations for standard sample were usually less than 0.75. The method was applied to the determination of chlorpromazine in proprietary drugs and results were statistically compared with the official British Pharmacopoeia (BP) method.

摘要

建立了一种新的简单流动注射分光光度法,用于在硫酸介质中使用铈(IV)测定氯丙嗪。在526nm的最大吸光度下监测药物的氧化形式。最佳条件为0.035M硫酸、3.80×10(-3)M铈(IV)、流速4.85ml/min、盘管长度45cm和进样量110mm(3)。采用改进的单纯形法进行优化。采用响应面法研究该方法的耐用性。采样频率达到120次/小时(-1)。标准样品的相对标准偏差通常小于0.75。该方法应用于测定专利药品中的氯丙嗪,并将结果与英国药典(BP)官方方法进行统计学比较。

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