Determination of Lead and Cadmium in Foods by Anodic Stripping Voltammetry: II. Collaborative Study

1982 ◽  
Vol 65 (4) ◽  
pp. 978-986
Author(s):  
Stephen G Capar ◽  
Raymond J Gajan ◽  
Elizabeth Madzsar ◽  
Richard H Albert ◽  
Marion Sanders ◽  
...  

Abstract A dry ash anodic stripping voltammetric method for determining lead and cadmium in foods was collaboratively studied by 20 laboratories. The food commodities studied were strained green beans, beef (baby food), fish (mackerel), infant formula (milk base), apple juice, and cereal (wheat farina). Each collaborator analyzed 3 commodities, each consisting of 2 duplicate lead and cadmium fortification levels, for a total of 4 samples for each commodity. The low fortification levels ranged from 0.03 to 0.08 ppm for cadmium and from 0.05 to 0.15 ppm for lead. The high fortification levels ranged from 0.12 to 0.28 ppm for cadmium and from 0.24 to 0.45 ppm for lead. Each commodity was analyzed by 10 collaborators. The average overall reproducibilities of the low level fortifications were 247c for lead and 21% for cadmium; for the high level fortifications, average overall reproducibilities were 18% for lead and 16% for cadmium. The average accuracies of the collaborative results as measured by comparison to reference values were 96 and 97% for cadmium and lead, respectively. This method has been adopted official first action.

2005 ◽  
Vol 37 (4) ◽  
pp. 709-713 ◽  
Author(s):  
Mónica Cecilia Vargas Mamani ◽  
Luiz Manoel Aleixo ◽  
Mônica Ferreira de Abreu ◽  
Susanne Rath

1983 ◽  
Vol 66 (6) ◽  
pp. 1414-1420
Author(s):  
Eric W Zink ◽  
Phillip H Davis ◽  
Reginald M Griffin ◽  
Wayne R Matson ◽  
Robert A Moffitt ◽  
...  

Abstract A method for the direct determination of lead in evaporated milk and in fruit juice with no prior sample digestion was successfully collaborated by 13 laboratories. The anodic stripping voltammetric (ASV) method studied consisted of adding 0.2 mL aliquots of evaporated milk or 0.3 mL aliquots of fruit juice to 2.9 mL of a dechelating reagent, Metexchange. The reagent-sample mixture is then analyzed for lead by ASV with no further sample preparation. Each collaborator received 24 samples, 2 each at 5 different levels (0.07-0.70 ppm for spiked evaporated milk and 0.09-0.87 ppm for spiked apple juice) along with duplicate practice samples of labeled lead content at each of 2 levels for each sample type. All unknowns were coded with random numbers. Approximately 69% of the reporting laboratories had never analyzed either evaporated milk or fruit juice for lead. Average time between receipt of samples and reporting of results was 1.6 days for all laboratories. The pooled variations between duplicate determinations for apple juice and evaporated milk were 0.00059 and 0.00043, respectively. The method was adopted official first action for both fruit juice and evaporated milk.


2013 ◽  
Vol 5 (1) ◽  
pp. 202-207 ◽  
Author(s):  
Luiz Carlos S. Figueiredo-Filho ◽  
Bruno C. Janegitz ◽  
Orlando Fatibelilo-Filho ◽  
Luiz Humberto Marcolino-Junior ◽  
Craig E. Banks

1982 ◽  
Vol 65 (4) ◽  
pp. 970-977
Author(s):  
Raymond J Gajan ◽  
Stephen G Capar ◽  
Cheryl A Subjoc ◽  
Marion Sanders

Abstract Food samples are dry ashed at 500 ± 50°C with a 10% aqueous K2SO4 solution used as an ashing aid. The ashed sample is dissolved in 50 mL 2% HNO3. Anodic stripping voltammetry is used to determine lead and cadmium in a mixture of the sample solution and an acetate electrolyte at pH 4.3 ± 0.3. The estimated quantitation limits, based on a 10 g food sample, are 0.005 ppm for cadmium and 0.010 ppm for lead.


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