Background Various tissue culture medium formulations currently are used to
transport, store and process stem and progenitor cells for transplantation
, although these solutions are not manufactured Jar clinical use.
Methods We have developed an infusible-grade solution, STM-Sav, for short-t
erm liquid cell storage and tested its ability to maintain viable functiona
l hematapoietic cells, compared with commonly-used tissue culture solutions
. G-CSF-stimulated normal-donor PBPC were stored in alpha-MEM, IMDM, RPMI-1
640, AIM 5, X-VIVO 10, PlasmaLyte A and STM-Sav, in gas-permeable Cryocyte
bags, at ambient temperature and 4 degrees C. The percentage of viable cell
s, percent recovery of viable mononuclear cells (MNC), percentage of CD34() cells, CFU-GM frequency and solution pH were determined for each solution
, at time points ranging from 0 to 72 h.
Results Cells were slightly better maintained nt 4 degrees C than at ambien
t temperature. No solution was superior to any other overall, although Plas
maLyte A was significantly inferior to all other solutions at preserving vi
able MNC. STM-Sav consistently maintained viable, functional cells as well
as, or better than in-vitro-use-only culture media, or PlasmaLyte A.
Discussion Cells could be stored in STM-Sav for at least 24 h at 4 degrees
C or ambient temperature, with recovery of approximately 90% of initial via
ble MNC, unchanged percentage CD34(+) cells and stable solution pH.