Jh. Crowe et al., STABILIZATION OF DRY MEMBRANES BY MIXTURES OF HYDROXYETHYL STARCH ANDGLUCOSE - THE ROLE OF VITRIFICATION, Cryobiology, 35(1), 1997, pp. 20-30
R. P. Goodrich and co-workers (1989, U.S. Patent 4,874,690; 1992, Proc
. Natl. Acad. Sci. LISA 89, 967-971) have reported that red blood cell
s can be preserved in the dry state by addition of mixtures of hydroxy
ethyl starch (HES) and glucose. More recently, Spieles and co-workers
(1996, Cryo-Lett. 17, 43-52) found that HES alone is insufficient to p
reserve the dry cells and concluded on this basis that the studies of
Goodrich er al. were incorrect. In the present paper we revisit that s
uggestion, using liposomes as a model to study effects of HES and gluc
ose on membrane stability. In previous studies we and others have esta
blished that liposomes can be stabilized in the dry state if they are
dried in the presence of disaccharides. Monosaccharides have not been
effective. Measurements of effects of glucose on phase transitions in
the dry lipids and vibrational frequency of the phosphate headgroup su
ggest that glucose shows an interaction with dry egg phosphatidylcholi
ne similar to that seen with disaccharides. Nevertheless, glucose does
not inhibit fusion in liposomes during drying, and it does not preven
t leakage. Hydroxyethyl starch, which has a very high glass transition
(T-g) inhibits fusion in the dry liposomes, but it does not depress t
he liquid crystalline to gel phase transition temperature (T-m) in the
dry phospholipids, does not cause a shift in the phosphate vibration
indicative of hydrogen bonding of the sugar to the phosphate, and does
not stop leakage of trapped carboxyfluorescein. However, if glucose i
s added to the HES-containing samples, the liposomes are stabilized, s
o long as the samples are maintained below the T-g of the mixture. If
they are heated above that T-g they fuse and leak their contents. We c
onclude that both glass formation and depression of T-m in the dry lip
ids are required. The role of glass formation in stabilization during
drying of liposomes appears to be inhibition of fusion. (C) 1997 Acade
mic Press.