Assay procedures for plasma concentrations of vitamin C, and hence for
vitamin C status, currently in use in European population surveillanc
e laboratories and elsewhere, are based on a wide range of disparate t
echniques and reactions. The problem of achieving harmonisation betwee
n these techniques, and between laboratories, is further complicated b
y the instability of the vitamin, and the existence of several chemica
l forms. In the course of a European Community FLAIR programme, of int
er-laboratory assay method comparisons for micronutrients, nine Europe
an laboratories performed either one or two coordinated ring tests, an
d some coordinated checks on in-house plasma samples, spiked with a lo
w level of ascorbic acid. The principal conclusion was that good agree
ment was difficult to obtain, between laboratories and between methods
, at plasma vitamin C concentrations close to the cut-off for biochemi
cal deficiency, i.e. ca. II mu M vitamin C in untreated plasma. By the
second ring test, and after the correction of some aberrant results d
ue to malfunctioning apparatus, interlaboratory coefficients of variat
ion of 13-20% were achieved, within the biochemically ''normal'' range
of 36-94 mu M. There remains, however; a need for critical within and
between-laboratory checks and comparisons, and for new quality contro
l materials, with assigned values.