Dh. Rhoney et al., Urokinase activity after freezing: Implications for thrombolysis in intraventricular hemorrhage, AM J HEAL S, 56(20), 1999, pp. 2047-2051
The retention of urokinase activity after frozen storage was studied.
Urokinase powder was reconstituted aseptically in sterile water for injecti
on or preservative-free 0.9% sodium chloride injection to a final concentra
tion of 5000 IU/mL. Samples were stored in 5mL. plastic syringes at -20 or
-70 degrees C for up to six months. Samples containing urokinase 25,000 IU/
mL were similarly prepared by using sodium chloride injection as the diluen
t and were stored frozen at the same temperatures for up to 93 days. Urokin
ase activity was measured with a chromogenic assay at each test interval. S
amples were also cultured after thawing to evaluate their potential to supp
ort microbial growth.
The activity of urokinase at either concentration did not change appreciabl
y during the study period. The method of thawing-at room temperature or in
a refrigerator-had no effect on urokinase activity. No microbial growth was
observed.
Urokinase 5000 IU/mL did not show any changes in activity when reconstitute
d with sterile water for injection or 0.9% sodium chloride injection and fr
ozen for up to six months. Urokinase 25,000 IU/mL in sodium chloride inject
ion was also stable after 93 days of frozen storage.