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悬浮培养中流体力学对动物细胞损伤的物理建模。

Physical modeling of animal cell damage by hydrodynamic forces in suspension cultures.

机构信息

Department of Chemical Engineering, University of Alberta, Edmonton, Alberta, Canada T6G 2G6.

出版信息

Biotechnol Bioeng. 1992 Dec 5;40(10):1277-81. doi: 10.1002/bit.260401018.

Abstract

Physical damage of animal cells in suspension culture, due to stirring and sparging, is coupled with complex metabolic responses. Nylon microcapsules, therefore, were used as a physical model to study the mechanisms of damage in a stirred bioreactor and in a bubble column. Microcapsule breaskage folowed first-order kinetices in all experiments Entrainment of bubbles into the liquid phase in the stirred bioreactor gave more microcapsule breakage. In the bubble column, the bubble bursting zone at gas-liquid interface was primarily responsible for microcapsule breakage. The forces on the microcapsules were equivalent to an external pressure of approximately 4 x 10(4) N. m(-2), based on the critical microcapsule diameter for survival of 190 microm. A stable foam layer, however, was found to be effective in protecting microcapsules from damage. The microcapsule transport to the gas-liquid interface and entrainment into the foam phase was consistent with flotation by air bubbles. This result implies that additives and operation of bioreactors should be selected to minimize flotation of cells.

摘要

悬浮培养的动物细胞由于搅拌和通气而受到的物理损伤与复杂的代谢反应有关。因此,尼龙微胶囊被用作物理模型来研究搅拌生物反应器和鼓泡塔中的损伤机制。在所有实验中,微胶囊的破裂都遵循一级动力学。搅拌生物反应器中气泡被带入液相会导致更多的微胶囊破裂。在鼓泡塔中,气-液界面的气泡破裂区是微胶囊破裂的主要原因。基于临界微胶囊直径为 190 微米时的生存压力,微胶囊上的力相当于约 4×10(4)N·m(-2)的外部压力。然而,发现稳定的泡沫层可有效防止微胶囊受损。微胶囊向气-液界面的输送和夹带进入泡沫相与气泡浮选一致。这一结果表明,应选择添加剂和生物反应器的操作条件,将细胞的浮选降至最低。

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