A New Integrated Lab-on-a-Chip System for Fast Dynamic Study of Mammalian Cells under Physiological Conditions in Bioreactor

For the quantitative analysis of cellular metabolism and its dynamics it is essential to achieve rapid sampling, fast quenching of metabolism and the removal of extracellular metabolites. Common manual sample preparation methods and protocols for cells are time-consuming and often lead to the loss of physiological conditions. In this work, we present a microchip-bioreactor setup which provides an integrated and rapid sample preparation of mammalian cells. The lab-on-a-chip system consists of five connected units that allow sample treatment, mixing and incubation of the cells, followed by cell separation and simultaneous exchange of media within seconds. This microsystem is directly integrated into a bioreactor for mammalian cell cultivation. By applying overpressure (2 bar) onto the bioreactor, this setup allows pulsation free, defined, fast, and continuous sampling. Experiments evince that Chinese Hamster Ovary cells (CHO-K1) can be separated from the culture broth and transferred into a new medium efficiently. Furthermore, this setup permits the treatment of cells for a defined time (9 s or 18 s) which can be utilized for pulse experiments, quenching of cell metabolism, and/or another defined chemical treatment. Proof of concept experiments were performed using glutamine containing medium for pulse experiments. Continuous sampling of cells showed a high reproducibility over a period of 18 h.

[1]  D. Fell Understanding the Control of Metabolism , 1996 .

[2]  J. Muller,et al.  Microfluidic device for the continuous preparation of eukaryotic cells for metabolic analysis , 2013, 2013 IEEE 26th International Conference on Micro Electro Mechanical Systems (MEMS).

[3]  I. Mezić,et al.  Chaotic Mixer for Microchannels , 2002, Science.

[4]  An-Ping Zeng,et al.  Mechanical disruption of mammalian cells in a microfluidic system and its numerical analysis based on computational fluid dynamics. , 2012, Lab on a chip.

[5]  Elmar Heinzle,et al.  Selective permeabilization for the high-throughput measurement of compartmented enzyme activities in mammalian cells. , 2011, Analytical biochemistry.

[6]  A. Bhagat,et al.  Inertial microfluidics for continuous particle separation in spiral microchannels. , 2009, Lab on a chip.

[7]  W. Tian,et al.  Introduction to Microfluidics , 2008 .

[8]  K. Jensen,et al.  Cells on chips , 2006, Nature.

[9]  Qiushui Chen,et al.  Qualitative and quantitative analysis of tumor cell metabolism via stable isotope labeling assisted microfluidic chip electrospray ionization mass spectrometry. , 2012, Analytical chemistry.

[10]  D. Di Carlo Inertial microfluidics. , 2009, Lab on a chip.

[11]  Marco Oldiges,et al.  Metabolomics: current state and evolving methodologies and tools , 2007, Applied Microbiology and Biotechnology.

[12]  M. Abdelgawad,et al.  Introduction to Microfluidics , 2006 .

[13]  Chih-Ming Ho,et al.  Cell Separation by Non-Inertial Force Fields in Microfluidic Systems. , 2009, Mechanics research communications.

[14]  M. Lane,et al.  A mild procedure for the rapid release of cytoplasmic enzymes from cultured animal cells. , 1979, Analytical biochemistry.

[15]  François,et al.  Improved protocols for quantitative determination of metabolites from biological samples using high performance ionic-exchange chromatography with conductimetric and pulsed amperometric detection. , 2000, Enzyme and microbial technology.

[16]  Jin-Ming Lin,et al.  Imitation of drug metabolism in human liver and cytotoxicity assay using a microfluidic device coupled to mass spectrometric detection. , 2012, Lab on a chip.

[17]  A. Zeng,et al.  A Chaotic Advection Enhanced Microfluidic Split-and-Recombine Mixer for the Preparation of Chemical and Biological Probes , 2012 .

[18]  D. Beebe,et al.  Physics and applications of microfluidics in biology. , 2002, Annual review of biomedical engineering.

[19]  G. Whitesides The origins and the future of microfluidics , 2006, Nature.