Berge T O, Jewett R L, Blair W O
Appl Microbiol. 1971 Nov;22(5):850-3. doi: 10.1128/am.22.5.850-853.1971.
A method was developed for freeze-dry stabilization of poliovirus type 3. An ultrafiltration procedure was used to remove salts from infected tissue culture fluid, and the virus was freeze-dried after suspension in an alkaline organic buffer. This method was further tested with other picornaviruses including poliovirus types 1 and 2, coxsackieviruses A9, A20, B2, and B5, echovirus 11, and the encephalomyocarditis virus. Freeze-dried preparations of the poliovirus could be shipped to distant laboratories at ambient temperature with excellent retention of infectivity. Data are presented showing effects of freeze-drying as well as results of exposure to temperatures to 37 C.
开发了一种用于3型脊髓灰质炎病毒冻干稳定化的方法。采用超滤程序从感染的组织培养液中去除盐分,病毒在碱性有机缓冲液中悬浮后进行冻干。该方法进一步用其他小核糖核酸病毒进行了测试,包括1型和2型脊髓灰质炎病毒、柯萨奇病毒A9、A20、B2和B5、埃可病毒11以及脑心肌炎病毒。脊髓灰质炎病毒的冻干制剂可以在环境温度下运往遥远的实验室,其感染力能得到很好的保留。文中给出了冻干效果以及暴露于37℃温度下的结果的数据。