کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6452138 1416998 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research PaperShear contributions to cell culture performance and product recovery in ATF and TFF perfusion systems
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله
Research PaperShear contributions to cell culture performance and product recovery in ATF and TFF perfusion systems
چکیده انگلیسی


- Poor product sieving in peristaltic pump TFF systems can be partly attributed to higher cell death rates.
- Peristaltic pumps used in TFF systems were the single major contributor to shear stress and cell lysis.
- Matching cell death rates eliminated sieving differences between TFF and ATF systems.
- A low shear pump for TFF perfusion was introduced as a feasible alternative to the ATF.

Achievement of a robust and scalable cell retention device remains a challenge in perfusion systems. Of the two filtration systems commonly used, tangential flow filtration (TFF) systems often have an inferior product sieving profile compared to alternating tangential flow filtration (ATF) systems, which is typically attributed to the ATF's unique alternating flow. Here, we demonstrate that observed performance differences between the two systems are a function of cell lysis and not the alternating flow as previously thought. The peristaltic pump used in typical TFF perfusion systems is shown to be the single major contributor to shear stress and cell lysis. Replacing the peristaltic pump with a low shear centrifugal pump brought cell growth, cell lysis, particle concentration, and product sieving in a TFF perfusion system to levels comparable with that of an ATF. These results provide a correlation where poor product sieving can be partially explained by high shear in cell retention systems and demonstrate that low shear TFF systems are a feasible alternative to ATF systems.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Biotechnology - Volume 246, 20 March 2017, Pages 52-60
نویسندگان
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