Avoidance of ice formation during cooling can be achieved by vitrification,
which is defined as solidification in an amorphous glassy state that obvia
tes ice nucleation and growth. We show that a vitrification approach to sto
ring vascular tissue results in markedly improved tissue function compared
with a standard method involving freezing. The maximum contractions achieve
d in vitrified vessels were >80% of fresh matched controls with similar dru
g sensitivities, whereas frozen vessels exhibited maximal contractions belo
w 30% of controls and concomitant decreases in drug sensitivity. In vivo st
udies of vitrified vessel segments in an autologous transplant model showed
no adverse effects of vitreous cryopreservation compared with fresh tissue
grafts.