Published September 26, 2007 | Version v1
Journal article

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

  • 1. Department of Oral Medicine, School of Dentistry, University of Granada, Granada (Spain)
  • 2. Department of Chemistry, Faculty of Sciences, University of Los Andes, Merida (Venezuela)

Description

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 (<0.4 mL 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 μL of either solution in the diluent stream. To avoid unnecessary waste of samples, the TBSI1 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 μL 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 deg. C), followed by pyrolysis and atomization at 700 and 1700 deg. C, respectively. The aqueous calibration was linear up to 120.0 μg 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 (3σ) was of 0.35 μg L-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 μg L-1 (mean of 55 ± 17 μg 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

Availability note (English)

Available from http://dx.doi.org/10.1016/j.aca.2006.10.021

Additional details

Identifiers

DOI
10.1016/j.aca.2006.10.021;
PII
S0003-2670(06)02064-2;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
600
Journal Issue
1-2
Journal Page Range
p. 214-220
ISSN
0003-2670
CODEN
ACACAM

Conference

Title
10. international conference on flow analysis
Dates
3-8 Sep 2006
Place
Porto (Portugal)

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
39051352
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
Resource subtype / Literary indicator
Conference
Descriptors DEI
ABSORPTION SPECTROSCOPY; ATOMIZATION; CALIBRATION; DETECTION; FLUID FLOW; FLUID INJECTION; GRAPHITE; PYROLYSIS; SALIVA; SOLENOIDS; ZINC
Descriptors DEC
BIOLOGICAL MATERIALS; BODY FLUIDS; CARBON; CHEMICAL REACTIONS; DECOMPOSITION; ELECTRIC COILS; ELECTRICAL EQUIPMENT; ELEMENTS; EQUIPMENT; MATERIALS; METALS; MINERALS; NONMETALS; SPECTROSCOPY; THERMOCHEMICAL PROCESSES

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.