Abstract
Modern measurement systems for food components often require use of ever smaller sample sizes, down to mg for some new microtechniques, which puts a stronger demand on development of reference materials with defined homogeneity for subsampling. One approach to evaluate the homogeneity of materials is the characterization of sampling constants, defined as that amount of material that gives a 1% error for subsampling. This approach was developed for geological sampling and has been applied in a limited way for inorganic components in food/biological materials. We have extended this approach to the determination of the sampling constants for an organic component, niacin, in the SRM 1846 Infant Formula material. This material was produced by blending of a dry vitamin mix (5% weight) into the bulk spray dried powder, for long term stability purposes. By analyzing similar aliquots of a reconstituted homogeneous fluid solution of a large sample size, in comparison to smaller portions of dry powder, an estimate of the variation due to sampling can be separated from estimates of variation due to analysis. Using either the AOAC microbiological method or a newly developed HPLC method, sampling constants for the niacin content of SRM 1846 are in the range of 1–3 g; use of smaller sub-samples can introduce significant variation into determinations using this SRM.
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Received: 25 May 1997 / Revised: 17 November 1997 / Accepted: 17 November 1997
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Wolf, W., Lacroix, D. Sampling constants for niacin content in standard reference material 1846 Infant Formula. Fresenius J Anal Chem 360, 459–464 (1998). https://doi.org/10.1007/s002160050739
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DOI: https://doi.org/10.1007/s002160050739