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宽表面积孔微滤膜在基于 TFF 的灌注细胞培养和连续生物加工的流体制备色谱集成中显著改善了筛分配制的衰减。

Wide-surface pore microfiltration membrane drastically improves sieving decay in TFF-based perfusion cell culture and streamline chromatography integration for continuous bioprocessing.

机构信息

Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey.

出版信息

Biotechnol Bioeng. 2020 Nov;117(11):3336-3344. doi: 10.1002/bit.27504. Epub 2020 Jul 30.

DOI:10.1002/bit.27504
PMID:32667680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7689868/
Abstract

Although several compelling benefits for bioprocess intensification have been reported, the need for a streamlined integration of perfusion cultures with capture chromatography still remains unmet. Here, a robust solution is established by conducting tangential flow filtration-based perfusion with a wide-surface pore microfiltration membrane. The resulting integrated continuous bioprocess demonstrated negligible retention of antibody, DNA, and host cell proteins in the bioreactor with average sieving coefficients of 98 ± 1%, 124 ± 28%, and 109 ± 27%, respectively. Further discussion regarding the potential membrane fouling mechanisms is also provided by comparing two membranes with different surface pore structures and the same hollow fiber length, total membrane area, and chemistry. A cake-growth profile is reported for the narrower surface pore, 0.65-µm nominal retention perfusion membrane with final antibody sieving coefficients ≤70%. Whereas the sieving coefficient remained ≥85% during 40 culture days for the wide-surface pore, 0.2-µm nominal retention rating membrane. The wide-surface pore structure, confirmed by scanning electron microscopy imaging, minimizes the formation of biomass deposits on the membrane surface and drastically improves product sieving. This study not only offers a robust alternative for integrated continuous bioprocess by eliminating additional filtration steps while overcoming sieving decay, but also provides insight into membranes' fouling mechanism.

摘要

尽管已有多项引人注目的生物工艺强化优势被报道,但仍需要简化灌流培养与捕获色谱的集成。在这里,通过使用具有宽表面积孔的微滤膜进行切向流过滤式灌流,建立了一种稳健的解决方案。所得到的集成式连续生物工艺在生物反应器中对抗体、DNA 和宿主细胞蛋白的保留率可忽略不计,平均筛分系数分别为 98±1%、124±28%和 109±27%。通过比较两种具有不同表面孔结构但具有相同中空纤维长度、总膜面积和化学性质的膜,进一步讨论了潜在的膜污染机制。对于较窄的表面孔,0.65-µm 名义保留灌流膜,报道了一个滤饼生长曲线,其最终抗体筛分系数≤70%。而对于宽表面积孔、0.2-µm 名义保留等级膜,筛分系数在 40 天的培养过程中保持≥85%。通过扫描电子显微镜成像证实的宽表面积孔结构最大限度地减少了在膜表面上生物质沉积物的形成,并极大地提高了产物的筛分。本研究不仅通过消除额外的过滤步骤并克服筛分衰减提供了一种稳健的集成连续生物工艺替代方案,还深入了解了膜的污染机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/d90b18e7d3a7/BIT-117-3336-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/c609d7f2d942/BIT-117-3336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/657e10f52ccf/BIT-117-3336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/ecc876f28cb6/BIT-117-3336-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/4898f14fac56/BIT-117-3336-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/7262c3d5f45c/BIT-117-3336-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/d90b18e7d3a7/BIT-117-3336-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/c609d7f2d942/BIT-117-3336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/657e10f52ccf/BIT-117-3336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/ecc876f28cb6/BIT-117-3336-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/4898f14fac56/BIT-117-3336-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/7262c3d5f45c/BIT-117-3336-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9d/7689868/d90b18e7d3a7/BIT-117-3336-g006.jpg

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本文引用的文献

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DNA RETENTION ON DEPTH FILTERS.DNA在深层过滤器上的保留
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Shift to high-intensity, low-volume perfusion cell culture enabling a continuous, integrated bioprocess.
端到端合作,变革生物制药研发与生产。
Biotechnol Bioeng. 2021 Sep;118(9):3302-3312. doi: 10.1002/bit.27688. Epub 2021 Feb 2.
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The Current Scientific and Regulatory Landscape in Advancing Integrated Continuous Biopharmaceutical Manufacturing.推进一体化连续生物制药制造的当前科学和监管格局。
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Progression of continuous downstream processing of monoclonal antibodies: Current trends and challenges.单克隆抗体连续下游处理的进展:当前趋势和挑战。
Biotechnol Bioeng. 2018 Dec;115(12):2893-2907. doi: 10.1002/bit.26812. Epub 2018 Oct 18.
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Larger Pore Size Hollow Fiber Membranes as a Solution to the Product Retention Issue in Filtration-Based Perfusion Bioreactors.大孔径中空纤维膜解决基于过滤的灌流生物反应器中的产物滞留问题。
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Mechanistic modeling of the loss of protein sieving due to internal and external fouling of microfilters.微滤器内部和外部污垢导致蛋白质筛分损失的机理建模。
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