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In this paper, we present cytotoxicity analysis (determination of lactate dehydrogenase — LDH activity performed in a designed and fabricated microfl uidic system. This method allowed for analysis of a supernatant collected from A549 (human lung cancer) and HT-29 (human colon cancer epithelial) cells, which were incubated for 24 h with selected compounds. LDH is an intracellular enzyme present in tissues, which is released into the supernatant caused by membrane damage or cell lyses. In our tests, LDH-Cytotoxicity Assay Kit (BioVision) was used. The toxic eff ect of drugs was measured in the developed microsystem made of PDMS (poly(dimethylsiloxane)). Analytical reaction took place in the special designed microchannel geometry. Then, the LDH activity was measured at 490 nm using spectrophotometer. In subsequent experiments, appropriate conditions for measurements using a microfl uidic system were chosen. It was found that the selected reagent is sensitive to temperature changes and light exposure. Reaction time in the microsystem was determined by changes of fl ow rates of reagents. Afterwards, for the various reaction time, the toxic eff ect of 5-fl uorouracil, celecoxib and 1,4-dioxane was performed. The obtained results were compared with the results carried out in 96-well plates. Based on these results, it was noted that the enzymatic reaction time in the microsystem is shorter than in 96-well plate. Moreover, the advantage of using microsystem is also the small amount of reagents.
Wydawca
Czasopismo
Rocznik
Tom
Strony
3--8
Opis fizyczny
Bibliogr. 20 poz., wykr., rys.
Twórcy
autor
- Department of Microbioanalytics, Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw
autor
autor
autor
Bibliografia
- [1] Kumar, S., and Prakash. “In vitro Models, Endpoints and Assessment Methods for the Measurement of Cytotoxicity”. Toxicol. Envir on. Health. Sci. 2 (2010): 87–93.
- [2] Weyermann, J., D. Lochmann, and A. Zimmer. “A practical note on the use of cytotoxicity assays”. Int. J. Pharmaceut 288 (2005): 369–376.
- [3] Eisenbrand, G., et al. “Methods of in vitro toxicology”. Food Chem Toxicol. 40 (2002): 193–236.
- [4] Racher, A.J., D. Looby, and J.B. Griffi ths. “Use of lactate dehydrogenase release to assess changes in culture viability”. Cytotechnology 3 (1990): 301–307.
- [5] Wolterbeek, H.T., and J.G.M. Meer. “Optimization, application, and interpretation of lactate dehydrogenase meaurements in microwell determination of cell number and toxicity”. Assay Drug Dev Technol 3 (2005): 675–682.
- [6] Haslam, G., D. Wyatt, and P.A. Kitos. “Estimating the number of viable animal cells in multi-well cultures based on their lactate dehydrogenase activities”. Cytotechnology 32 (2000): 63–75.
- [7] Niles, A.L., R.A. Moravec, and T.L. Riss. “In Vitro Viability and Cytotoxicity Testing and Same-Well Multi-Parametric Combinations for High Throughput Screening”. Current Chemical Genomics 3 (2009): 33–41.
- [8] Baudoin, R., et al. “Behavior of HepG2/C3A cell cultures in a microfluidic bioreactor”. Biochemical Engineering Journal 53 (2001): 172–181.
- [9] Lee, P.J., et al. “Microfl uidic System for Automated Cellbased Assays:. JALA Charlottesv Va 12 (2007): 363–367.
- [10] Midwoud, P.M., et al. “Microfluidic Biochip for the Perifusion of Precision-Cut Rat Liver Slices for Metabolism and Toxicology Studies”. Biotechnology and Bioengineering 105 (2010): 184–194.
- [11] Hattersley, S.M., J. Greenman, and S.J. Haswel. “Study of ethanol induced toxicity in liver explants using microfl uidic devices”. Biomed Microdevices 13 (2011): 1005--1014.
- [12] Hattersley, S.M., et al. “A Microfluidic System for Testing the Responses of Head and Neck Squamous Cell Carcinoma Tissue Biopsies to Treatment with Chemotherapy Drugs”. Annals of Biomedical Engineering 1 (2011): 1277--1288.
- [13] 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.
- [14] Jędrych, E., et al. “Evaluation of cytotoxic eff ects of 5-fl uorourcil on human carcinoma cells in microfl uidic system”. Sensors and Actuators B 160 (2011): 1544–1551.
- [15] Lim, Y.J., et al. “Celecoxib attenuates 5-fl uorouracil--induced apoptosis in HCT-15 and HT-29 human colon cancer cells”. World J Gastroenterol 13 (2007): 1947–1950.
- [16] Réti, A., et al. “Enhancement of 5-Fluorouracil Effi cacy on High COX-2 Expressing HCA-7 Cells by Low Dose Indomethacin and NS-398 but not on Low COX-2 Expressing HT-29 Cells”. Pathol. Oncol. Res. 15 (2009): 335–344.
- [17] Kan, H., et al. “Cyclooxygenase-independent downregulation of multidrug resistance–associated protein-1 expression by celecoxib in human lung cancer cells”. Mol Cancer Ther 4 (2005): 1358.
- [18] Hasinoff , B., D. Patel, and X. Wu. “The cytotoxicity of celecoxib towards cardiac myocytes is cyclooxygenase-2 independent”. Cardiovascular Toxicology 7 (2007) 19--27.
- [19] Blume, C., et al. “Cerivastatin inhibits proliferation of interleukin-1β-induced ratmesangialcells by enhanced formation of nitric oxide”. Europ. J. Pharmacol. 485 (1), 2004: 1–10.
- [20] Huhtala, A., et al. “The Eff ects of 5-Fluorouracil on Ocular Tissues In Vitro and In Vivo after Controlled Release from a Multifunctional Implant”. Invest. Ophthalmol. Vis. Sci. 50 (2009): 2216–2223.
Typ dokumentu
Bibliografia
Identyfikator YADDA
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