Slurry preparation by high-pressure homogenization for cadmium, copper and lead determination in cervine liver and kidney by electrothermal atomic absorption spectrometry

• Published in: Analyst (London) 1996-04, Vol.121 (4), p.483-488
• Main Authors: YANXI TAN, MARSHALL, W. D, BLAIS, J.-S
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Cadmium - analysis; Copper - analysis; Deer; Food industries; Fundamental and applied biological sciences. Psychology; Lead - analysis; Liver - chemistry; Meat and meat product industries; Pressure; Spectrophotometry, Atomic - methods
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/AN9962100483

Homogenization with a flat valve homogenizer in combination with high-speed blending was evaluated for the preparation of slurries suitable for the ETAAS determination of cadmium, copper and lead concentrations in six SRMs and in frozen cervine liver and kidney. Fresh tissue (approximately 2 g) or powdered SRM (approximately 0.1 g) was dispersed, at high speed, in 20 ml of ethanol-water (1 + 9 v/v) containing 0.25% m/m tetramethylammonium hydroxide. The resulting suspension was passed through a high-pressure flat valve homogenizer. Determinations performed on the resulting homogenate, provided estimates for Cd, Pb and Cu concentrations that were within 27, 23 and 18% of the certified values, respectively, for the six SRMs. In all instances, the experimental results did not differ significantly from the certified values. For frozen tissues there was good agreement between the concentrations as determined by slurry homogenization-ETAAS and conventional digestion-ICP-MS. In addition, no significant differences were detected between the slopes of the calibration curves for external standards and standard additions to homogenized sample (SRMs or fresh tissue). Moreover, replicate determinations of analyte concentrations in slurries at various times post-preparation did not detect any segregation of the homogenates during 6 d. For these matrices at least, short-term sample storage had no discernible effect on the analyte apparent concentrations. The applicability of the process was limited only by the levels of contaminating Pb and Cu introduced into the sample by the homogenizer.