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Determination of aluminum in highly concentrated iron samples: Study of interferences using high-resolution continuum source atomic absorption spectrometry
Authors:Denise Bohrer  Uwe Heitmann  Mao-dong Huang  Helmut Becker-Ross  Stefan Florek  Bernhard Welz  Denise Bertagnolli
Institution:1. Departamento de Química Universidade Federal de Santa Maria, 97110-905 Santa Maria, RS, Brazil;2. ISAS, Institute for Analytical Sciences, Department for Interface Spectroscopy, Albert-Eistein Street 9, 12489 Berlin, Germany;3. Instituto de Química, Departamento de Química Analítica, Universidade Federal da Bahia, 40170-290 Salvador, BA, Brazil
Abstract:High-resolution continuum source atomic absorption spectrometry (HR-CS AAS) has been used to investigate spectral and non-spectral interferences found with a conventional line source atomic absorption spectrometer in the determination of aluminum in pharmaceutical products containing elevated iron and sugar concentrations. A transversely heated graphite furnace was used as the atomizer in both spectrometers. The two most sensitive aluminum lines at 309.3 nm and 396.2 nm were investigated and it was found that an iron absorption line at 309.278 nm, in the vicinity of the aluminum line at 309.271 nm, could be responsible for some spectral interference. The simultaneous presence of iron and the organic components of the matrix were responsible for radiation scattering, causing high continuous and also structured background absorption at both wavelengths. The aluminum and iron absorption could not be separated in time, i.e., the iron interference could not be eliminated by optimizing the graphite furnace temperature program. However, an interference-free determination of aluminum was possible carrying out the measurements with HR-CS AAS at 396.152 nm after applying least squares background correction for the elimination of the structured background. Analytical working range and other figures of merit were determined and are presented for both wavelengths using peak volume registration (center pixel ± 1) and the center pixel only. Limits of detection and characteristic masses ranged from 1.1 to 2.5 pg and 13 to 43 pg, respectively. The method was used for the determination of the aluminum contamination in pharmaceutical formulations for iron deficiency treatment, which present iron concentrations from 10 to 50 g l− 1. Spike recoveries from 89% to 105% show that the proposed method can be satisfactorily used for the quality control of these formulations.
Keywords:High-resolution continuum source atomic absorption spectrometry  Aluminum determination  Iron matrix  Spectral interferences  Pharmaceutical formulations
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