A major limitation in the quantitative accuracy of the human lymphocyt
e micronucleus (MN) assay is preservation of the cytoplasm during the
cell harvesting. In this short communication, an improved method for c
ytoplasm preservation in a cytokinesis-blocked, whole-blood microcultu
re (0.3 ml) technique is described. We believe that the timing of the
hypotonic treatment, speed of centrifugation, handling of the cell sus
pension and proper Giemsa staining are important variables in the huma
n peripheral lymphocyte MN assay.