A liquid chromatography method for analysis of phenoxymethylpenicillin
has been examined in a collaborative study involving 6 laboratories.
The method comprised an isocratic part, which is used in the assay, Wh
en the isocratic part is combined with gradient elution, the method is
suitable for purity control. Five samples of phenoxymethylpenicillin
(potassium salts and acid) were analysed. The main component, the most
important side product 4-hydroxyphenoxymethylpenicillin and other imp
urities were determined. An analysis of variance proved the absence of
consistent laboratory bias. Laboratory-sample interaction was not sig
nificant. Estimates of the repeatability and reproducibility of the me
thod, expressed as standard deviations (SD) of the result of the deter
mination of phenoxymethylpenicillin, were 0.50 and 0.63 respectively.