Abstract

A microdigestion procedure for the determination of Cd and Cu in biological samples by graphite furnace atomic absorption spectrometry (GF AAS) is described. Masses up to 5 mg are directly weighed in the autosampler cup and 100 µL of the digestion solution (1:1 v/v HNO3-H2SO4 or concentrated HNO3) are added. The cups are closed and the digestion is performed, at 60 oC overnight in a specially designed digestion block. After cooling, 900 µL of ultrapure water is added, the solution is homogenized and the cups are transferred to the autosampler tray. Since the digestion is performed in a sealed environment and the whole procedure uses only one flask, the risks of contamination and losses are minimized. Calibration was performed with external calibration curves, in the same medium as the reagents blank. The analysis of nine different standard reference materials permitted the assessment to the accuracy of the procedure. Considering a 5 mg sample mass, the limits of quantification in the original samples calculated from ten successive measurements of the blank solution (k=10) were 0.07 and 1.7 and 0.02 and 0.3 µg g-1 for Cd and Cu respectively, using the HNO3-H2SO4 mixture or concentrated HNO3 for the digestion. The procedure was used for the determination of Cu in human liver biopsy samples.

Highlights

  • The sample dissolution or digestion is still the most common sample pre-treatment in total trace analysis, since a low viscosity liquid isA Microdigestion Procedure Directly Performed in the Autosampler CupsJ

  • Optimum pyrolysis and atomization temperatures were obtained from pyrolysis and atomization temperatures curves performed in the blanks, prepared by the 1+9 (v/v) dilution of the digestion solutions (1+1 v/v HNO3:H2SO4 and concentrated HNO )

  • The proposed method proved to be feasible for the digestion of different kinds of biological samples

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Summary

Introduction

The sample dissolution or digestion is still the most common sample pre-treatment in total trace analysis, since a low viscosity liquid (preferably an aqueous solution) isA Microdigestion Procedure Directly Performed in the Autosampler CupsJ. A Microdigestion Procedure Directly Performed in the Autosampler Cups. Solid sampling (SS) is an alternative and techniques such as solid sampling electrothermal vaporization associated to inductively coupled plasma mass spectrometry (SS-ETV-ICP-MS) or solid sampling graphite furnace atomic absorption spectrometry (SS-GF AAS) are examples of such possibility.[2,3] Solid sampling is claimed to avoid the risks of contamination and losses that are related to sample digestion, and since no dilution occurs, excellent limits of detection in the original samples can be obtained. Typical problems related to solid sampling still impair the spread of its acceptance in routine analysis: Due to the small sample masses usually used 4,5 problems related to sample non-homogeneity may be experienced; since the use of aqueous calibration solutions is not always possible, calibration problems may be observed

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