全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
Cells  2013 

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

DOI: 10.3390/cells2020349

Keywords: biomicrofluidics, lab-on-a-Chip, mammalian cells, metabolism, integrated bioreactor

Full-Text   Cite this paper   Add to My Lib

Abstract:

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.

References

[1]  Groussac, E.; Ortiz, M.; Fran?ois, J. Improved protocols for quantitative determination of metabolites from biological samples using high performance ionic-exchange chromatography with conductimetric and pulsed amperometric detection. Enzyme Microb. Technol. 2000, 26, 715–723.
[2]  Fell, D. Understanding the Control of Metabolism, 1st ed.; Portland Press: Portland, OR, USA, 1997.
[3]  Oldiges, M.; Lütz, S.; Pflug, S.; Schroer, K.; Stein, N.; Wiendahl, C. Metabolomics: Current state and evolving methodologies and tools. Appl. Microbiol. Biotechnol. 2007, 76, 495–511, doi:10.1007/s00253-007-1029-2.
[4]  Wurm, M.; Zeng, A.-P. Mechanical disruption of mammalian cells in a microfluidic system and its numerical analysis based on computational fluid dynamics. Lab Chip 2012, 12, 1071, doi:10.1039/c2lc20918g.
[5]  Tsutsui, H.; Ho, C.-M. Cell separation by non-inertial force fields in microfluidic systems. Mech. Res. Commun. 2009, 36, 92–103, doi:10.1016/j.mechrescom.2008.08.006.
[6]  Kuntaegowdanahalli, S.S.; Bhagat, A.A.S.; Kumar, G.; Papautsky, I. Inertial microfluidics for continuous particle separation in spiral microchannels. Lab Chip 2009, 9, 2973, doi:10.1039/b908271a.
[7]  Whitesides, G.M. The origins and the future of microfluidics. Nature 2006, 442, 368–373, doi:10.1038/nature05058.
[8]  Beebe, D.J.; Mensing, G.A.; Walker, G.M. Physics and applications of microfluidics in biology. Annu. Rev. Biomed. Eng. 2002, 4, 261–286.
[9]  Tabeling, P. Introduction to Microfluidics; Oxford University Press: Oxford, NY, USA, 2010.
[10]  El-Ali, J.; Sorger, P.K.; Jensen, K.F. Cells on chips. Nature 2006, 442, 403–411, doi:10.1038/nature05063.
[11]  Mao, S.; Gao, D.; Liu, W.; Wei, H.; Lin, J.-M. Imitation of drug metabolism in human liver and cytotoxicity assay using a microfluidic device coupled to mass spectrometric detection. Lab Chip 2012, 12, 219–226, doi:10.1039/c1lc20678h.
[12]  Chen, Q.; Wu, J.; Zhang, Y.; Lin, J.-M. Qualitative and quantitative analysis of tumor cell metabolism via stable isotope labeling assisted microfluidic chip electrospray ionization mass spectrometry. Anal. Chem. 2012, 84, 1695–1701, doi:10.1021/ac300003k.
[13]  Rajabi, N.; Bahnemann, J.; Tzeng, T.-N.; Zeng, A.-P.; Müller, J. Microfluidic device for the continuous preparation of eukaryotic cells for metabolic analysis. In Micro Electro Mechanical Systems (MEMS), Proceedings of the 2013 IEEE 26th International Conference on, Taipei, Taiwan, 20–24 January 2013; pp. 259–262.
[14]  Rajabi, N.; Bahnemann, J.; Wahrheit, J.; Heinzle, E.; Zeng, A.-P.; Müller, J. Inertia-based media exchange and quenching of cells for the continuous preparation of cells in a lab-on-a-chip. In proceedings of the 3rd European Conference on Microfluidics, Heidelberg, Germany, 4–5 December 2012.
[15]  Rajabi, N.; Hoffmann, M.; Bahnemann, J.; Zeng, A.-P.; Schlüter, M.; Müller, J. A Chaotic Advection Enhanced Microfluidic Split-and-Recombine Mixer for the Preparation of Chemical and Biological Probes. J. Chem. Eng. Japan 2012, 45, 703–707, doi:10.1252/jcej.12we071.
[16]  Stroock, A.D. Chaotic Mixer for Microchannels. Science 2002, 295, 647–651.
[17]  Di Carlo, D. Inertial microfluidics. Lab Chip 2009, 9, 3038, doi:10.1039/b912547g.
[18]  Mackall, J.; Meredith, M.; Lane, M. A mild procedure for the rapid release of cytoplasmic enzymes from cultured animal cells. Anal. Biochem. 1979, 95, 270–274, doi:10.1016/0003-2697(79)90216-1.
[19]  Niklas, J.; Melnyk, A.; Yuan, Y.; Heinzle, E. Selective permeabilization for the high-throughput measurement of compartmented enzyme activities in mammalian cells. Anal. Biochem. 2011, 416, 218–227.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413