Lute Scott, Wang Hua, Sanchez Davonie, Barletta Janet, Chen Qi, Brorson Kurt
Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, USA.
Biologicals. 2009 Oct;37(5):331-7. doi: 10.1016/j.biologicals.2009.07.002. Epub 2009 Aug 15.
Virus removal studies are used to insure the safety of biopharmaceutical products by quantitatively estimating the viral clearance capacity by the manufacturing process. Virus quantification assays are used to measure the log(10) clearance factor of individual purification unit operations in spike recovery studies. We have developed a multiplex RT Q-PCR assay that detects and quantifies three commonly used model viruses X-MuLV, SV40, and MMV simultaneously. This RT Q-PCR multiplex assay has a 6log(10) dynamic range with a limit of detection (LOD) of approximately 1 genome copy/microL. Amplification profiles are similar to existing singleplex assays. Overall, this RT Q-PCR multiplex assay is highly quantitative, accurately identifies multiple viruses simultaneously, and may prove useful to validate viral clearance of biological products in small scale studies.
病毒去除研究用于通过定量评估生产过程的病毒清除能力来确保生物制药产品的安全性。病毒定量分析用于在加标回收研究中测量各个纯化单元操作的log(10)清除因子。我们开发了一种多重RT Q-PCR分析方法,可同时检测和定量三种常用的模型病毒X-MuLV、SV40和MMV。这种RT Q-PCR多重分析方法具有6log(10)的动态范围,检测限(LOD)约为1个基因组拷贝/微升。扩增曲线与现有的单重分析方法相似。总体而言,这种RT Q-PCR多重分析方法具有高度的定量性,能够同时准确鉴定多种病毒,并且在小规模研究中可能被证明有助于验证生物制品的病毒清除情况。