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跨膜压力对与血管性血友病因子共表达的重组人凝血因子VIII在ATF灌注培养中凝血因子VIII产量的影响。

Effect of transmembrane pressure on Factor VIII yield in ATF perfusion culture for the production of recombinant human Factor VIII co-expressed with von Willebrand factor.

作者信息

Kim Seung-Chul, An Sora, Kim Hyun-Ki, Park Beom-Soo, Na Kyu-Heum, Kim Byung-Gee

机构信息

Research Institute, Dong-A Socio-Holdings Co., Ltd., Yong-in, 449-900, Republic of Korea.

Interdisciplinary Program for Bioengineering, Seoul National University, Seoul, 151-742, Republic of Korea.

出版信息

Cytotechnology. 2016 Oct;68(5):1687-96. doi: 10.1007/s10616-015-9918-1. Epub 2015 Oct 13.

Abstract

In this study, we evaluated three cell retention devices, an alternating tangential flow (ATF) system, a spin-filter, and a Centritech Lab III centrifuge, for the production of recombinant human Factor VIII co-expressed with von Willebrand factor. From the results, it was found that the FVIII activity in bioreactor was significantly higher in the ATF perfusion culture than two other perfusion cultures. Moreover, the FVIII activity yield was unexpectedly low in the ATF perfusion culture. We have, therefore, studied the reasons for this low FVIII activity yield. It was revealed that the inactivation and the surface adsorption of FVIII onto the harvest bag were not the main reasons for the low yield in the ATF perfusion culture. The FVIII activity yield was not increased by the use of a hollow fiber filter with 0.5 μm pore size instead of 0.2 μm pore size. Additionally, the retention of FVIII molecules by the hollow fiber filter was a dominant factor in the low FVIII activity yield in the ATF perfusion culture. We demonstrated that FVIII yield was significantly improved by controlling transmembrane pressure (TMP) across the hollow fiber filter membrane. Taken together, these results suggest that TMP control could be an efficient method for the enhancement of FVIII yield in an ATF perfusion culture.

摘要

在本研究中,我们评估了三种细胞截留装置,即交替切向流(ATF)系统、旋转过滤器和Centritech Lab III离心机,用于生产与血管性血友病因子共表达的重组人凝血因子VIII。从结果中发现,在生物反应器中,ATF灌注培养中的FVIII活性显著高于其他两种灌注培养。此外,ATF灌注培养中的FVIII活性产量出人意料地低。因此,我们研究了这种低FVIII活性产量的原因。结果表明,FVIII的失活以及其在收获袋上的表面吸附并非ATF灌注培养中产量低的主要原因。使用孔径为0.5μm而非0.2μm的中空纤维过滤器并没有提高FVIII活性产量。此外,中空纤维过滤器对FVIII分子的截留是ATF灌注培养中FVIII活性产量低的主要因素。我们证明,通过控制中空纤维过滤膜的跨膜压力(TMP),FVIII产量可显著提高。综上所述,这些结果表明,TMP控制可能是提高ATF灌注培养中FVIII产量的有效方法。

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