Optimized procedure for the determination of antimony in lipid-rich environmental matrices by flow injection hydride generation atomic absorption spectrometry

Abstract

An analytical procedure for the reliable determination of Sb in digests of lipid-rich environmental matrices in the low ng l^–1-range based on flow injection hydride generation atomic absorption spectrometry (FI-HG-AAS) has been developed. Prior to HG-AAS, aliquots (250 to 320 mg) of dry samples were mineralized with 3 ml nitric acid and 0.5 ml of each sulfuric and perchloric acids in open digestion vessels made of glassy carbon in a heating block. Procedure detection and quantification limits of a previously developed procedure for the determination of Sb in plant materials by FI-HG-AAS were decreased with respect to the lower Sb concentrations in animal tissues, the sensitivity of the instrumental response was increased, and the composition of the acid digestion mixture was re-optimized for lipid-rich samples. The accuracy and precision of the developed procedure was evaluated by the analysis of the two reference materials Bovine Liver 1577a and Pig Kidney CRM 186. These reference materials have been additionally spiked with appropriate amounts of Sb to obtain recovery data. The solution detection limit (3ς) in digested samples was 0.021 µg l^–1, the detection limit for the whole procedure based on the dry powders was 7 pg g^–1, the method quantification limit for a reliable determination of Sb was 23 pg g^–1. The reproducibility of repetitive measurements was 6.0% at 0.1 µg Sb l^–1 and 2.2% at 0.5 µg Sb l^–1. Calibration curves were linear from 0.05 to 3 µg Sb l^–1. To demonstrate the suitability of the developed method, concentrations of Sb have been determined in pigeon eggs (≡2 ng Sb g^–1), as well as in bream livers (≡4 ng g^–1) and in deer livers (≡5 to 8 ng g^–1) from animals living in remote and urban-industrialized areas of Germany, respectively.