PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Powiadomienia systemowe
  • Sesja wygasła!
  • Sesja wygasła!
  • Sesja wygasła!
Tytuł artykułu

Potentiometric detection of the metabolic activity of human tumor cells

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Monitoring of cellular viability is a key part of toxicological assays in vitro. On-line monitoring of metabolic activity would be particularly useful for evaluation of responses to potential therapeutic compounds. Current assays are mostly based on fluorescent dyes and optical detection methods. These methods offer high sensitivity and specificity, however are not suitable for long-term on-line observations. Electrochemical methods can be an alternative for current protocols. Electrochemical detection is low cost and label-free, therefore suitable for long-term cell culture monitoring. In this work investigations on human cancer cells viability will be presented. Cells were cultured as two-dimensional monolayer or three-dimensional spheroids. Different cell culture media were examined. Potentiometric detection was used for continuous monitoring of cell culture as well as end-point investigations. Different growth phases were identified using applied method. Finally, response to an anticancer drug was successfully observed.
Rocznik
Strony
41--46
Opis fizyczny
Bibliogr. 30 poz., rys., wykr.
Twórcy
  • Department of Microbioanalytics, Institute of Biotechnology, Warsaw University of Technology
autor
autor
autor
autor
Bibliografia
  • [1] “World Cancer report 2008”, IARC (WHO), 2008.
  • [2] 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.
  • [3] Yamada, K., and E. Cukierman. “Modeling tissue morphogenesis and Cancer in 3D.” Cell 130 (2007): 601–610.
  • [4] Lin, R., and H. Chang. “Recent advances in three-dimensional multicellular spheroid culture for biomedical research.” Biotechnology Journal 3 (2008): 1172–1184.
  • [5] Sutherland, R. “Cell and Environmet Interactions in Tumor Microregions: The Multicell Spheroid Model.” Science 240 (1988): 177–184.
  • [6] Kim, J. “Three-dimensional tissue culture models in cancer biology”. Seminars in Cancer Biology 15 (2005): 365–377.
  • [7] Fischbach, C., et al. “Engineering tumors with 3D scaffolds.” Nature Methods 4 (2007): 855–860.
  • [8] Pampaloni, F., E. Stelzer, and A. Masoti. “Three-Dimensional Tissue Models for Drug Discovery and Toxicology.” Recent Patents on Biotechnology 3 (2009): 103–117.
  • [9] 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.
  • [10] Kelm, J., et al. “Method for Generation of Homogenous Multicellular Tumor Spheroid Applicable to a Wide Variety of Cell Types.” Biotechnology and Bioengineering 83 (2003): 173–180.
  • [11] Torisawa, Y., et al. “A multicellular spheroid array to realize spheroid formation, culture, and viability assay on a chip.” Biomaterials 28 (2007): 559–566.
  • [12] Friedrich, J., R. Ebner, and L. Kunz-Schughart. “Experimental anti-tumor therapy in 3-D: Spheroids—old hat or new challenge?”. International Journal of Radiation Biology 83 (2007): 849–871.
  • [13] Pampaloni, F., and E. Stelzer. “Three-Dimensional Cell Cultures in Toxicology”. Biotechnology and Genetic Engineering Reviews 26 (2009): 129–150.
  • [14] Griffith, L., and M. Swartz. “Capturing complex 3D tissue physiology in vitro.” Nature Reviews Molecular Cell Biology 7 (2006): 211–224.
  • [15] The Ethics of Research Involving Animals. 2005.
  • [16] EU directive no 2001/83/EC (2001).
  • [17] Rangarajan, A., et al. “Species- and cell type-specific requirements for cellular transformation”. Cancer Cell 6 (2004): 171–183.
  • [18] Sivaraman, A., et al. “A Microscale In Vitro Physiological Model of the Liver: PredicitiveScreens for Drug Metabolism and Enzyme Induction”. Current Drug Metabolism 6 (2005): 569–591.
  • [19] Ziółkowska, K., et al. “Long-term three-dimensional cell culture and anticancer drug activity evaluation in a microfluidic chip”. Biosensors and Bioelectronics 40 (2013): 68–74.
  • [20] Ziółkowska, K., et al. „Development of a three-dimensional microfluidic system for long term tumor spheroid culture”. Sensors and Actuators B 173 (2012): 908–913.
  • [21] Ziółkowska, K., et al. “Novel designs and technologies for cell engineering”. Challenges of Modern Technology 2 (2011): 54–60.
  • [22] Ziółkowska, K., et al. “PDMS/Glass microfluidic cell culture system for cytotoxicity tests and cells passage.” Sensors and Actuators B 145 (2010): 533–542.
  • [23] Walker, G., M. Ozers, and D. Beebe. “Insect Cell Culture in Microfluidic Channels”. Biomedical Microdevices 4 (2002):161–166.
  • [24] Hsiao, A., et al. “Microfluidic system for formation of PC-3 prostate cancer co-culture spheroids”. Biomaterials 30 (2009): 3020–3027.
  • [25] Alberts, B., et al. Essential cell biology: an introduction to the molecular biology of the cell. New York–London: Garland Publishing, Inc., 1997.
  • [26] Freshner, R. Culture of Animal Cells: A Manual of Basic Technique. 5th Edition. Hoboken, New Jersey: John Wiley and Sons, Inc., 2005.
  • [27] Balagadde, F., et al. “Long-term Monitoring of Bacteria Undergoing Programmed Population Control in a Microchemostat”. Science 309 (2005): 137–140.
  • [28] Chudy, M., et al. “Miniaturized tools and devices for bioanalytical applications: an overview.” Analytical and Bioanalytical Chemistry 395 (2009): 647–668.
  • [29] Berridge, M., et al. “The biochemical and cellular basis of cell proliferation assays that use tetrazolium salts”. Biochemica 4 (1996): 14–19.
  • [30] Ziółkowska, K., et al. “Multiwell plate reader-compatible microfluidic system for long-term multicellular spheroid culture and monitoring”. Proceedings of the 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences “MicroTAS 2012”. 2012: 407–409.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-07816bf4-67f9-47e8-b27c-3df5dbb73e62
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.