Flow analysis-hydride generation-Fourier transform infrared spectrometric determination of antimony in pharmaceuticals

被引:25
|
作者
Gallignani, M [1 ]
Ayala, C [1 ]
Brunetto, MR [1 ]
Burguera, M [1 ]
Burguera, JL [1 ]
机构
[1] Univ Los Andes, Fac Sci, IVAIQUIM, Venezuelan Andean Inst Chem Res, Merida 5101A, Venezuela
关键词
antimony determination; stibine; SbH3; glucantime; flow analysis; hydride generation; Fourier transform infrared spectrometry;
D O I
10.1016/S0039-9140(02)00648-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a flow analysis system with hydride generation and Fourier transform infrared (FTIR) spectrometric detection has been developed for the determination of antimony in pharmaceuticals. The method is based on the on-line mineralization/oxidation of the organic antimonials present in the sample and pre-reduction of Sb(V) to Sb(III) with K2S2O8 and KI, respectively; prior to the stibine generation. The gaseous SbH3 is separated from the solution in a gas phase separator, and transported by means of a nitrogen carrier into a short pathway (10 cm) IR gas cell, where the corresponding FTIR spectrum is acquired by accumulating 3 scans in a continuous mode. The 1893 cm(-1) band was used for the quantification of the antimony. The procedure is carried out in a closed system, which reduces sample handling and makes possible the complete automation of the antimony determination. The figures of merit of the proposed method (linear range: 0-600 mg l(-1), limit of detection (3sigma) = 0.9 mg l(-1), limit of quantification (IOU) = 3 mg Sb l(-1), precision (R.S.D.) less than 1% and sample frequency=28 h(-1)), are appropriate for the designed application. Furthermore, precise and accurate results were found for the analysis of different antimonial pharmaceutical samples, indicating that the methodology developed represents a valid alternative for the determination of antimony in pharmaceuticals, which could be suitable for the routine control analysis. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:923 / 934
页数:12
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