Wickerhauser M, Williams C, Kolen B L, Busby T F
Plasma Derivatives Laboratory, American Red Cross Laboratories, Rockville, Md.
Vox Sang. 1987;53(1):1-6. doi: 10.1111/j.1423-0410.1987.tb04904.x.
Heat stability of lyophilized C1 inactivator (C1-INA) concentrates of intermediate and high purity has been investigated under several heat treatment protocols that include heating for 96 and 192 h at 68 degrees C and for 10 h at 80, 90 and 100 degrees C. Both types of concentrate showed high stability in functional activity, with not more than 5% loss in any of the time-temperature combinations evaluated. However, the C1-INA antigen from both concentrates showed small but progressive changes in crossed immunoelectrophoretic pattern, in proportion to the intensity of heat treatment. High-pressure size-exclusion chromatography revealed only minimal signs of aggregation in the high-purity concentrate, but a significant and progressive aggregation of nonspecific protein contaminants present in the intermediate-purity concentrate, making the high-purity concentrate preferable for heat treatment.
已在几种热处理方案下研究了中高纯度冻干C1灭活剂(C1-INA)浓缩物的热稳定性,这些方案包括在68℃下加热96小时和192小时,以及在80℃、90℃和100℃下加热10小时。两种类型的浓缩物在功能活性方面均表现出高稳定性,在所评估的任何时间-温度组合中损失均不超过5%。然而,两种浓缩物中的C1-INA抗原在交叉免疫电泳图谱中均显示出微小但渐进的变化,与热处理强度成比例。高压尺寸排阻色谱显示,高纯度浓缩物中仅出现极少量的聚集迹象,但中纯度浓缩物中存在的非特异性蛋白质污染物出现明显且渐进的聚集,这使得高纯度浓缩物更适合进行热处理。