Flow-Injection Iodimetric Determination of Captopril in Pharmaceutical Preparations

被引:23
|
作者
Schmidt, Erlando, Jr. [1 ]
Melchert, Wanessa R. [1 ]
Rocha, Fabio R. P. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, BR-05513970 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
flow injection; spectrophotometry; iodimetry; captopril; anti-hypertensive; CHEMILUMINESCENCE DETERMINATION; SPECTROPHOTOMETRIC DETERMINATION; SENSITIVE DETERMINATION;
D O I
10.1590/S0103-50532009000200007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A simple, fast and low cost procedure for spectrophotometric determination of captopril in pharmaceutical preparations is described. The procedure is based on a flow-injection system exploiting the on-line formation of the triiodide reagent, which is consumed in the presence of the analyte generating a transient signal. Linear response was observed up to 200 mu mol L-1 with a detection limit of 1.0 mu mol L-1 (99.7% confidence level). The coefficient of variation (n = 20) and the sampling rate were estimated as 1.2% and 72 determinations per hour, respectively. The main excipients found in pharmaceutical preparations did not affect the captopril determination. The zone sampling approach was exploited to implement on-line dilutions, aiming direct analysis of sample extracts. Results of the analysis of commercial samples agreed with the obtained by the titrimetric reference procedure described in the US-Pharmacopeia at the 95% confidence level. The reagent consumption was estimated as 18 mu g of KMnO4 and 10 mg of KI per determination, with a cost of US$ 2.50 per 1000 determinations.
引用
收藏
页码:236 / 242
页数:7
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