Analytical Methods Committee AMCTB No. 78
First published on 6th July 2017
Proficiency testing of analytical laboratories is now ubiquitous—laboratories need to participate regularly to receive accreditation. The outcome helps participants to detect unexpected sources of uncertainty. But sampling, as well as analysis per se, introduces its own uncertainty in most types of analysis. Sampling uncertainty arises partly from heterogeneity in the ‘target’ (the particular mass of material for which the sample is a surrogate), but also from variation in the manner in which the sample is extracted. Different samplers will do the job somewhat differently, even when following a single protocol. The potential value of proficiency tests for sampling is therefore obvious. And in recent years, feasibility studies and schemes have appeared in several application sectors. Different sectors have very different constraints on how sampling and proficiency testing can be carried out. Nevertheless, the need for general guidelines is obvious.
• We can’t send the target to the participants: nearly always the samplers will have to travel to the target.
• The samplers usually can’t have one target each. They will all have to use the same target sequentially, which implies that, to preserve independence, the target must be capable of being restored to its original appearance and, possibly its original constitution, between each sampling episode. For the same reason, the samplers should not see each other at work.
• The target must be acceptably close to stable in composition over the period in which the samplers operate.
• The target will not necessarily be effectively homogeneous. In extreme cases, differences among samplers could be overwhelmed by the heterogeneity of the target.
• Unless all of the samplers use the same detailed protocol, it is impossible to separate between-protocol variance and between-sampler variance (this applies equally to analysis).
• The composition of each sample has to be determined by analysis, which adds further component of uncertainty to the outcome. Moreover, there are two options for the analysis: having all of the analysis undertaken in one laboratory, or each sampler separately commissioning the analysis of their own sample.
• The target will in most instances comprise a valuable commodity, and owners will not want its value to be reduced by the exercise.
Phew! These difficulties, however, were recognised from early considerations of uncertainty from sampling1–3 and have been addressed in various ways. In newly emerging applications, or where some doubt exists about the validity of the sampling protocol, some preliminary validation would be required before proficiency testing could be usefully undertaken. That could be tackled by a series of randomised replicated experiments to estimate the variance components associated with different targets, protocols, samplers, samples and analysis. The protocol could then be suitably tailored to match the qualities of the target material and the requirements of fitness for purpose (unless it was a protocol prescribed by a regulator).
While the different sources of variation in results might be untangled by a randomised replicated experiment, such designs do not lend themselves to use in a proficiency test, where a participant needs a score analogous to the z-score, z = (x − xpt)/σpt derived from a result x, an assigned value xpt, and a fitness-for-purpose criterion σpt that is independent of the results.
Even in some established application areas, however, there is no uniformly accepted protocol. In such instances the results will inseparably reflect the variation among the protocols, as well as in the performance of the samplers (including their skill in choosing the most appropriate protocol).
A different approach involves each participant organisation providing its own analytical result. That in effect regards the sampling and analysis as a unitary measurement operation for determining the composition of the target. In that circumstance, the fitness criterion should address the combined uncertainty (that is, sampling plus analytical).
In some media (gases in particular), an alternative assigned value can be obtained by spiking the test material with a known concentration of the analyte. In that case the assigned value can be determined independently of the participants’ results, so the question of correlation does not arise.
M. H. Ramsey (University of Sussex) and M. Thompson (Birkbeck University of London).
This Technical Brief was prepared by the Subcommittee for Uncertainty from Sampling and approved by the Analytical Methods Committee on 06/06/17.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c7ay90092a |
This journal is © The Royal Society of Chemistry 2017 |