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Process Development of Adenoviral Vector Production in Fixed Bed Bioreactor: From Bench to Commercial Scale

机译:固定床生物反应器中腺病毒载体生产的过程开发:从长凳到商业规模

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Large-scale vector manufacturing for phase III and beyond has proven to be challenging. Upscaling the process with suspension cells is increasingly feasible, but many viral production applications are still applicable only in adherent settings. Scaling up the adherent system has proven to be troublesome. The iCELLis((R)) disposable fixed-bed bioreactors offer a possible option for viral vector manufacturing in large quantities in an adherent environment. In this study, we have optimized adenovirus serotype 5 manufacturing using iCELLis Nano with a cultivation area up to 4m(2). HEK293 cell cultivation, infection, and harvest of the virus (by lysing the cells inside the bioreactor) proved possible, reaching total yield of up to 1.6x10(14) viral particles (vp)/batch. The iCELLis 500 is designed to satisfy demand for large-scale requirements. Inoculating a large quantity of cell mass into the iCELLis 500 was achieved by first expanding the cell mass in suspension. Upscaling the process into an iCELLis 500/100m(2) cultivation area cassette was practical and produced up to 6.1x10(15) vp. Flask productivity per cm(2) in iCELLis Nano and iCELLis 500 was in the same range. As a conclusion, we showed for the first time that iCELLis 500 equipment has provided an effective way to manufacture large batches of adenoviral vectors.
机译:III阶段和超越的大规模矢量制造已被证明是挑战性的。升级悬浮电池的过程越来越可行,但许多病毒生产应用仍然仅适用于粘附的设置。缩放贴壁系统已被证明是麻烦的。 Icellis((r))一次性固定床生物反应器为粘附环境中大量的病毒载体制造提供了可能的选择。在这项研究中,我们使用Icellis Nano优化了腺病毒血清型5制造,其栽培面积高达4M(2)。 HEK293细胞培养,感染和收获病毒(通过裂解生物反应器内的细胞),证明可能,达到最高1.6×10(14)病毒颗粒(VP)/批次的总产量。 Icellis 500旨在满足对大规模要求的需求。通过首先扩张悬浮液中的细胞物质,通过将大量的细胞质量分解到Icellis 500中来实现。将该过程升高到Icellis 500 / 100m(2)栽培区域盒式盒的实用性并产生高达6.1x10(15)vp。 Icellis Nano和Icellis 500中每厘米(2)的烧瓶生产率在相同的范围内。作为结论,我们首次展示了Icellis 500设备提供了制造大批腺病毒载体的有效方法。

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