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C G van de Kamp

Publications and source records attributed to C G van de Kamp.

5 recordsLinked to original sources

Aluminium determination in food matrices IUPAC check sample survey of analytical performance.

Aluminum has been determined by 24 laboratories in the context of a check sample survey. Samples studied were two duplicate diets, one of which was spiked with 15.87 mg Al/kg, and two blind duplicate milk powders. Target values for the duplicate diets were 11.80 and 27.90 mg Al/kg, respectively, and 15.65 mg Al/kg for the milk powders. Participants were requested to make only single determinations per sample. A two-step approach was used to assess the raw data. In the first step, those data were excluded that were outside a +/- 50% range of the duplicate diet spike and the target value for milk powder. Likewise, only one single data set per participant was accepted and results were ruled out stemming from procedures that have a detection limit of greater than 5 mg Al/kg. The remaining data were evaluated both statistically and in the context of the method performance parameters available. Best scores for aluminium were from laboratories applying wet-pressurized digestion in combination with electrothermal atomic absorption spectrometry. Results for laboratories applying dry-ashing for sample decomposition were unreliable. The overall performance for aluminium is very disappointing given the relatively high aluminium levels of the samples studied. Out of 24 laboratories 11 have one or more major problems with their aluminium determination. They should dramatically improve or replace their methodology for this element.

Aluminum↗

Some elements in domestic and imported fresh fruits marketed in The Netherlands.

Sodium, potassium, arsenic, selenium and tin have been determined in 38 different types of domestic and imported fresh fruits. All samples (n = 242) were analysed for Na und K whereas a limited number of samples (n = 85) of each fruit type was selected for the determination of As, Se and Sn. The median contents, in mass fractions of the edible portion, found for fresh fruits are: Na less than 0.001%; K 0.17%; As 4 micrograms/kg; Se 2 micrograms/kg and Sn less than 0.05 mg/kg. The corresponding 90th percentile values are: Na 0.002%, K 0.34%; As 12 micrograms/kg; Se 10 micrograms/kg and Sn 0.10 mg/kg. Results for selenium reported here differ substantially from those given for a number of fresh fruits in the German Food Composition Tables 1986/1987. The average consumption of 129 g fresh fruit by Dutch citizens in the age category of 22-75 years contributes, in general, marginally to the total daily dietary intake of sodium, arsenic, selenium and tin. Fresh fruit can contribute substantially, up to 23%, to the average oral daily intake of potassium.

Arsenic↗

Reference-material-based collaborative test of flame atomic absorption spectroscopic determination of calcium and magnesium in foods and biological materials.

A flame atomic absorption spectroscopic (FAAS) method is described for the determination of calcium and magnesium in a wide variety of foods and biological substrates. Results for reference materials (n = 9) are presented that demonstrate the validity of the procedure. Samples are digested with nitric acid at 150 degrees C in a pressure decomposition vessel, diluted and adjusted to pH 2 with ammonia. Lanthanum chloride solution is added to suppress phosphate interferences and the ionization of calcium and magnesium in the AAS flame. Additional dilutions are made as appropriate, whereupon the atomic absorption of calcium and magnesium is measured in an oxidizing air-acetylene flame. The wavelength settings for calcium is 422.7 nm and for magnesium 285.2 nm. The method was tested in a collaborative trial involving a milk powder practice sample and four test samples, all of which were reference materials. Participants were requested to carry out duplicate determinations exclusively. Results were obtained from 12 laboratories. However, the results of 3 laboratories had to be rejected for various reasons. The remaining set of data was statistically evaluated according to ISO 5725; the method of analysis proved to be precise and accurate. Coefficients of variation values for calcium ranged from 1.19% to 4.44% within laboratories (CVr) and from 5.30% to 15.9% between laboratories (CVR). For magnesium, the corresponding values were CVr, 1.07% to 3.52% and CVR, 3.07% to 5.99%. The method is recommended for the determination of calcium and magnesium at the levels considered in foods and biological substrates.

Animals↗

Preparation and stability of ampouled polycyclic aromatic hydrocarbon solutions.

A 1-year stability study of ampouled polycyclic aromatic hydrocarbon (PAH) solutions was carried out. Two solutions of seven pure PAHs were prepared, one in acetonitrile and one in toluene, and ampouled. Solutions were tested for mass concentration and impurities before and after ampouling. No differences were found. After 0, 3, 6, 9 and 12 months, three ampoules were selected for analysis from the acetonitrile and the toluene lots stored at +20 degrees and at -20 degrees C. The acetonitrile solution was analysed by high performance liquid chromatography and the toluene solution by glass capillary gas chromatography. The results demonstrate that both solutions were stable and no contamination occurred during storage.

Food Analysis↗