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Aggregate Removal Nanofiltration of Human Serum Albumin Solution Using Nanocellulose-Based Filter Paper

机译:纳米纤维素滤纸聚集人血清白蛋白溶液的聚集纳米过滤

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摘要

This study is dedicated to the rapid removal of protein aggregates and viruses from plasma-derived human serum albumin (HSA) product to reduce the risk of viral contamination and increase biosafety. A two-step filtration approach was implemented to first remove HSA aggregates and then achieve high model virus clearance using a nanocellulose-based filter paper of different thicknesses, i.e., 11 μm (prefilter) and 22 μm (virus filter) at pH 7.4 and room temperature. The pore size distribution of these filters was characterized by nitrogen gas sorption analysis. Dynamic light scattering (DLS) and size-exclusion high performance liquid chromatography (SE-HPLC) were performed to analyze the presence of HSA aggregates in process intermediates. The virus filter showed high clearance of a small-size model virus, i.e., log reduction value (LRV) > 5, when operated at 3 and 5 bar, but a distinct decrease in LRV was detected at 1 bar, i.e., LRV 2.65–3.75. The throughput of HSA was also dependent on applied transmembrane pressure as was seen by Vmax values of 110 ± 2.5 L m and 63.6 ± 5.8 L m at 3 bar and 5 bar, respectively. Protein loss was low, i.e., recovery > 90%. A distribution of pore sizes between 40 nm and 60 nm, which was present in the prefilter and absent in the virus filter, played a crucial part in removing the HSA aggregates and minimizing the risk of virus filter fouling. The presented results enable the application of virus removal nanofiltration of HSA in bioprocessing as an alternative to virus inactivation methods based, e.g., on heat treatment.
机译:本研究致力于从血浆衍生的人血清白蛋白(HSA)产品中快速去除蛋白质聚集体和病毒,以降低病毒污染和增加生物安全性的风险。实施了两步过滤方法以首先去除HSA聚集体,然后使用在pH 7.4和室内的不同厚度的基于纳米纤维素的滤纸,即11μm(预滤器)和22μm(病毒过滤器)的纳米纤维素的滤纸来实现高模型病毒间隙温度。这些过滤器的孔径分布的特征在于氮气吸附分析。进行动态光散射(DLS)和尺寸排除高效液相色谱(SE-HPLC)以分析过程中间体中HSA聚集体的存在。病毒过滤器显示出小尺寸模型病毒的高间隙,即在3和5巴在3和5巴操作时,对数值减少值(LRV)> 5,但在1巴,即LRV 2.65-中检测到LRV的不同降低。 3.75。 HSA的产量也依赖于所施加的跨膜压力,其vmax值分别在3巴和5巴的3℃和5巴的63.6±5.8L m。蛋白质损失低,即回收> 90%。在预滤器中存在的40nm和60nm之间的孔径的分布在病毒过滤器中存在,在除去HSA聚集体并最小化病毒滤波器污垢的风险中起关键部分。所呈现的结果使得病毒去除纳米过滤在生物处理中的应用作为基于热处理的病毒失活方法的替代方案。

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