Flow injection on-line dilution for zinc determination in human saliva with electrothermal atomic absorption spectrometry detection

被引:20
作者
Burguera-Pascu, Margarita [1 ]
Rodriguez-Archilla, Alberto
Burguera, Jose Luis
Burguera, Marcela
Rondon, Carlos
Carrero, Pablo
机构
[1] Univ Granada, Sch Dent, Dept Oral Med, Granada, Spain
[2] Univ Los Andes, Fac Sci, Dept Chem, Merida, Venezuela
关键词
on-line dilution; flow injection-electrothermal atomic absorption spectrometry (FI-ET AAS); saliva samples; baseline zinc levels; contamination-free determination;
D O I
10.1016/j.aca.2006.10.021
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An automated method is described for the determination of zinc in human saliva by electrothermal atomic absorption spectrometry (ET AAS) after on-line dilution of samples with a significant reduction of sample consumption per analysis (<0.4mL including the dead volume of the system). in order to fulfill this aim without changing the sample transport conduits during the experiments, a flow injection (FI) dilution system was constructed. Its principal parts are: one propulsion device (peristaltic pump, PP) for either samples, standards or washing solution all located in an autosampler tray and for the surfactant solution (Triton X-100) used as diluent, and a two-position time based solenoid injector (TBSI1) which allowed the introduction of 10 mu L of either solution in the diluent stream. To avoid unnecessary waste of samples, the TBSI, also permitted the recirculation of the solutions to their respective autosampler cups. The downstream diluted solution fills a home made sampling arm assembly. The sequential deposition of 20 mu L, aliquots of samples or standards on the graphite tube platform was carried out by air displacement with a similar time based solenoid injector (TBSI2). The dilution procedure and the injection of solutions into the atomizer are computer controlled and synchronized with the operation of the temperature program. Samples or standards solutions were submitted to two drying steps (at 90 and 130 degrees C), followed by pyrolysis and atomization at 700 and 1700 degrees C, respectively. The aqueous calibration was linear up to 120.0 mu g L-1 for diluted standard solutions/samples and its slope was similar (p > 0.05) to the standard addition curve, indicating lack of matrix effect. The precision tested by repeated analysis of real saliva samples was less than 3% and the detection limit (3 sigma) was of 0.35 mu gL(-1). To test the accuracy of the proposed procedure, recovery tests were performed, obtaining mean recovery of added zinc of 97.8 +/- 1.3%. Furthermore, Zn values estimated by the procedure developed in this work were compared with those obtained by a standard addition flame-AAS method applied to 20 randomly selected saliva samples. No significant differences (p > 0.05) were obtained between the two methods. Zinc levels in saliva samples from 44 healthy volunteers, 15 male and 29 female, with ages between 20 and 51 years (mean 30.50 +/- 9.14 years) were in the range 22-98 mu g L-1 (mean of 55 17 mu g L-1), similar to some and different from others reported in the literature. It was found that zinc values for male were statistically higher (p = 0.006) than for female. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:214 / 220
页数:7
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