O'Grady J, Losikoff A, Poiley J, Fickett D, Oliver C
Department of Process Biochemistry, Medlmmune, Inc. Gaithersburg, MD, USA.
Dev Biol Stand. 1996;88:319-26.
Nanofiltration of immunoglobulin products was investigated as a virus removal step using Planova-controlled pore size membranes. For these studies, purified preparations of an IgG and an IgM were tested with 15 nm and 35 nm Planovace nanofiltration membranes, respectively. The results of spiking studies with four model viruses indicated that both the Planova 15 and 35 membranes removed 6-7 log10 plaque or focus forming units of murine xenotropic retrovirus, simian virus 40 and pseudorabies virus. Although two tandem Planova 35 membranes were tested for clearance of poliovirus, only the Planova 15 membrane removed this virus. Nanofiltration experiments were carried out with protein concentrations up to 12 mg/ml for the IgG and 1-2 mg/ml for the IgM, and protein recovery was excellent.
使用普兰诺娃(Planova)控制孔径的膜,对免疫球蛋白产品的纳滤作为病毒去除步骤进行了研究。在这些研究中,分别用15纳米和35纳米的普兰诺娃(Planova)纳滤膜对一种IgG和一种IgM的纯化制剂进行了测试。对四种模型病毒进行加样研究的结果表明,普兰诺娃15和35膜均去除了6-7个对数10的小鼠嗜异性逆转录病毒、猿猴病毒40和伪狂犬病病毒的蚀斑或灶形成单位。尽管测试了两个串联的普兰诺娃35膜对脊髓灰质炎病毒的清除情况,但只有普兰诺娃15膜能去除这种病毒。纳滤实验在IgG蛋白浓度高达12毫克/毫升和IgM蛋白浓度为1-2毫克/毫升的条件下进行,蛋白质回收率极佳。