Article ID Journal Published Year Pages File Type
3748 Biochemical Engineering Journal 2011 6 Pages PDF
Abstract

Mass transport phenomena in cell culture can be formulated by using classical reaction-diffusion equations; however, in practice, it is difficult to solve these equations analytically. Here, we used computer simulation to solve these equations, and compared the time-dependent concentration profile of substances in conventional static culture with that in perfusion culture. The simulated glucose consumption in static culture agreed with that of actual culture conditions used in a general cell culture experiment. The simulation of perfusion culture revealed that the geometry of the chamber and its operating parameters are critical to obtaining a sufficient supply of substances. We also found that the previously reported perfusion chambers are well designed and operate under adequate conditions. Our kinetic model of time-dependent concentration profiles for general substances based on mass transport phenomena could, therefore, be used for the optimal design of a microfluidic perfusion culture chip.

► Mathematical modeling was used to assess substance supply in cell cultures. ► Simulation of static culture conditions resembles actual culture conditions. ► Simulation was used to evaluate previously reported perfusion chambers. ► The mathematical model could be use to design a microfluidic cell culture chip.

Related Topics
Physical Sciences and Engineering Chemical Engineering Bioengineering
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