As a cell sorter, Sedimentation field-flow fractionation (SdFFF) can be def
ined as an effective tool for cell separation and purification, respecting
integrity and viability as well as providing enhanced recovery and purified
sterile fraction collection. The complex cell suspension containing both n
eurons and glial cells of all types, obtained from cerebral cortices of 17-
day-old rat fetuses, is routinely used as a model of primary neuronal cultu
re. Using SdFFF, this complex cell mixture was eluted in sterile fractions
which were collected and Cultured. SdFFF Cell elution was conducted under s
trictly defined conditions: rapid cell elution, high recovery (negligible c
ell trapping), short- and long-term cell viability, sterile collection. Aft
er immunological cellular type characterization (neurons and glial cells) o
f cultured cells, our results demonstrated the effectiveness of SdFFF to pr
ovide, in less than 6 min, viable and enriched neurons which can be culture
d for further investigations. (C) 2001 Elsevier Science B.V. All rights res
erved.