The Advanced Centre for Biochemical Engineering, Department of Biochemical Engineering, University College London, Torrington Place, London WC1E 7JE, UK.
Biotechnol Bioeng. 2011 Apr;108(4):830-8. doi: 10.1002/bit.23013. Epub 2010 Dec 22.
Flat-sheet membrane discs represent the current standard format used for experimental prediction of the scale-up of normal flow filtration processes. Use of this format is problematic, however, since the scale-down results typically show a 40-55% difference in performance compared to large-scale cartridges depending upon the feedstock used. In this work, novel pleated scale-down devices (Am=1.51-15.1×10(-3) m2) have been designed and fabricated. It is shown that these can more accurately predict the performance of industrial scale single-use pleated membrane cartridges (Am=1.06 m2) commonly used within biopharmaceutical manufacture. The single-use scale-down cartridges retain the same pleat characteristics of the larger cartridges, but require a reduced feed volume by virtue of a substantially diminished number of active membrane pleats. In this study, a 1,000-fold reduction in feed volume requirement for the scale-down cartridge with the smallest membrane area was achieved. The scale-down cartridges were tested both with clean water and a pepsin protein solution, showing flux-time relationships within 10% of the large-scale cartridge in both cases. Protein transmission levels were also in close agreement between the different scale cartridges. The similarity in performance of the scale-down and the large-scale cartridges, coupled with the low feed requirement, make such devices an excellent method by which rapid scale-up can be achieved during early stage process development for biopharmaceutical products. This new approach is a significant improvement over using flat-sheet discs as the quantitative similarity in performance with the large-scale leads to reliable scale-up predictions while requiring especially small volumes of feed material.
平板膜片代表了当前用于预测常规流量过滤过程放大的标准格式。然而,由于根据使用的原料,这种格式的缩小结果通常与大尺寸筒式过滤器相比性能差异为 40-55%,因此使用这种格式存在问题。在这项工作中,设计并制造了新颖的褶式缩小装置(Am=1.51-15.1×10(-3) m2)。结果表明,这些装置可以更准确地预测工业规模一次性褶式膜筒(Am=1.06 m2)的性能,这种膜筒在生物制药生产中通常被使用。一次性缩小筒保留了较大筒的相同褶状特征,但由于有效膜褶的数量大大减少,因此需要减少进料体积。在这项研究中,最小膜面积的缩小筒的进料体积需求减少了 1000 倍。用清洁水和胃蛋白酶蛋白溶液对缩小筒进行了测试,在这两种情况下,通量-时间关系都与大尺寸筒相差 10%以内。不同尺寸的缩小筒之间的蛋白质传输水平也非常一致。缩小筒和大尺寸筒之间的性能相似,再加上低进料需求,使得这些装置成为生物制药产品早期工艺开发过程中快速放大的极好方法。与使用平板膜片相比,这种新方法是一个重大改进,因为与大尺寸筒的定量相似性可以带来可靠的放大预测,同时需要的进料量特别小。