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Novel designs and technologies for cell engineering

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Microfluidic devices, such as lab-on-a-chip systems, are highly advantageous for cell engineering and cell based assays. It is a particularly useful approach for development of the in vitro cellular systems mimicking the in vivo environment. In this paper, a novel lab-on-a-chip device for three-dimensional human cell culture and anticancer drug testing is presented. Cells were cultured as Multicellular Tumor Spheroids (MCTS) — the best cancer tumor model developed so far. Diff erent designs were tested and novel technique of microfabrication in poly(dimethylsiloxane) was developed. MCTS were cultured in a system of polymeric microwells, with the network of microfluidic channels for culture medium flow. Design included optimal shear stress and proper nutrients supply for cultured cells. Final design provided MCTS culture for four weeks with the homeostasis-like state achievement, which is characteristic for the in vivo situation.
Rocznik
Strony
54--60
Opis fizyczny
Bibliogr. 39 poz., rys.
Twórcy
  • Department of Microbioanalytics, Institute of Biotechnology, Warsaw University of Technology
autor
autor
autor
Bibliografia
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  • [5] Guillouzo, A., and C. Guguen-Guillouzo. “Evolving concepts in liver tissue modelling and implications for in vitro toxicology.” Expert Opinion on Drug Metabolism and Toxicology 4 (2008): 1279–1294.
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  • [10] Borenstein, J., et al. “Microfabrication Technology for Vascularized Tissue Engineering.” Biomedical Microdevices 4 (2002): 167–175.
  • [11] Cunningham, K., and A. Gotlieb “The role of shear stress in the pathogenesis of atherosclerosis.” Laboratory Investigation 85 (2005): 9–23.
  • [12] Blackman, B., G. Garcia-Cardena, and M. Gimbrone. “A New In Vitro Model to Evaluate Diff erential Responses of Endothelial Cells to Simulated Arterial Shear Stress Waveforms” Journal of Biomechanical Engineering 124 (2002): 397–407.
  • [13] Keane, J., D. Ryan, and P. Gray. “Effect of Shear Stress on Expression of a Recombinant Protein by Chinese Hamster Ovary Cells.” Biotechnology and Bioengineering 81 (2003): 211–220.
  • [14] Seo, S., et al. “Enhanced liver functions of hepatocytes cocultured with NIH 3T3 in the alginate/galactosylated chitosan scaff old.” Biomaterials 27 (2006): 1487–1495.
  • [15] Ziółkowska, K., R. Kwapiszewski, and Z. Brzózka. “Microfluidic devices as tools for mimicking the in vivo environment.” New Journal of Chemistry 35 (2011): 979--990.
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  • [17] Andersson, H., and A. Van Den Berg. “Microfabrication and microfl uidics for tissue engineering: state of the art and future opportunities.” Lab on a Chip 4 (2004): 98–103.
  • [18] Bhadriraju, K., and C. Chen “Engineering cellular microenvironments to improve cell-based drug testing.” Drug Discovery Today 7 (2002): 612–620.
  • [19] Park, T., and M. Shuler. “Integration of Cell Culture and Microfabrication Technology.” Biotechnology Progress 19 (2003): 243–253.
  • [20] Shim, J., et al. “Micro- and Nanotechnologies for Studying Cellular Function.” Current topics in medicinal chemistry 3 (2003): 687–703.
  • [21] Leclerc, E., Y. Sakai, and T. Fujii. “Cell Culture in 3-Dimensional Microfluidic Structure of PDMS (polydimethylsiloxane).” Biotechnology Progress 20 (2004): 750–755.
  • [22] Walker, G., H. Zeringue, and D. Beebe. “Microenvironment design considerations for cellular scale studies”. Lab on a Chip 4 (2004): 91–97.
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  • [24] Poland, J., et al. “Comparison of protein expression profiles between monolayer and spheroid cell culture of HT-29 cells revealed fragmentation of CK18 in three--dimensional cell culture.” Electrophoresis 23 (2002):1174–1184.
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  • [27] Ziółkowska, K., et al. “Lab-on-a-chip for cell engineering: towards cellular models mimicking in vivo.” Challenges of Modern Technology 1.2 (2011): 79–82.
  • [28] Torisawa, Y., et al. “A multicellular spheroid array to realize spheroid formation, culture, and viability assay on a chip.” Biomaterials 28 (2007): 559–566.
  • [29] Ziółkowska, K., et al. “PDMS/Glass microfl uidic cell culture system for cytotoxicity tests and cells passage.” Sensors and Actuators B 145 (2010): 533–542.
  • [30] Velve-Casquillas, G., et al. “Microfluidic tools for cell biological research.” Nano Today 5 (2010): 28–47.
  • [31] McDonald, J., and G. Whitesides. “Poly(dimethylsiloxane) as a Material for Fabricating Microfluidic Devices.” Accounts of Chemical Research 35 (2002): 491–499.
  • [32] Regehr, K., et al. “Biological implications of polydimethylsiloxane-based cell culture.” Lab on a Chip 9 (2009):2132–2139.
  • [33] McDonald, J., et al. “Fabrication of microfluidic systems in poly(dimethylsiloxane).” Electrophoresis 21 (2000): 27--40.
  • [34] Becker, H., and C. Gärtner. “Polymer microfabrication technologies for microfl uidic systems.” Analytical and Bioanalytical Chemistry 390 (2008): 89–111.
  • [35] Wong, I., and C. Ho. “Surface molecular property modifications for poly(dimethylsiloxane) (PDMS) based microfluidic devices.” Microfl uidics and Nanofl uidics 7 (2009): 291–306.
  • [36] Briones, M., et al. “Practical Method for Rapid Microchannel Fabrication in Polydimethylsiloxane by Replica Molding without Using Silicon Photoresist.” Journal of Chemical Engineering of Japan 39 (2006): 1108–1114.
  • [37] Koerner, T., et al. “Epoxy resins as stamps for hot embossing of microstructures and microfl uidic channels.” Sensors and Actuators B 107 (2005): 632–639.
  • [38] Gitlin, L., P. Schulze, and D. Belder. “Rapid replication of master structures by double casting with PDMS.” Lab on a Chip 9 (2009): 3000–3002.
  • [39] Eddington, D., J. Puccinelli, and D. Beebe. “Thermal aging and reduced hydrophobic recovery of polydimethylsiloxane.” Sensors and Actuators B 114 (2006): 170–172.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b8df68b5-16d8-4c7c-acc5-4f0c949af75b
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