MODELING DRUG DELIVERY IN GRAVITY-DRIVEN MICROFLUIDIC SYSTEM

被引:0
作者
Maki, Antti-Juhana [1 ]
Kreutzer, Joose [1 ]
Kallio, Pasi [1 ]
机构
[1] Tampere Univ Technol, Dept Automat Sci & Engn, FIN-33101 Tampere, Finland
来源
PROCEEDINGS OF THE ASME 12TH INTERNATIONAL CONFERENCE ON NANOCHANNELS, MICROCHANNELS, AND MINICHANNELS, 2014 | 2014年
关键词
CULTURE; CELLS;
D O I
暂无
中图分类号
TH [机械、仪表工业];
学科分类号
0802 ;
摘要
Human cells cultivated in a microfluidic system provide an interesting alternative for animal experiments in drug screening. For these tests, a pumpless system based on hydrostatic pressure could be used for drug delivery. The objective of this paper is to provide a method to analyze drug distribution in a gravity-driven microfluidic system to reduce the design cycle of these systems. The approach is based on an analytical model combined with a finite element method (FEM). The paper presents simulation of gravity-driven drug delivery in a polydimethylsiloxane (PDMS)-based microfluidic cell culture system. In the study, a simple but commonly used system including two reservoirs, inlet and outlet, connected through a microchannel, is modeled. In the proposed method, time-dependent working pressure based on hydrostatic and capillary pressures is first approximated analytically. Secondly, using the calculated pressure, a velocity profile of single-phase fluid flow is solved across the system using the FEM. Finally, a distribution of a selected drug compound over the system is simulated and analyzed. Based on the results, the initial geometry is improved for better performance. The paper demonstrates how the modified system provides faster and more uniform drug concentration profile on the cells compared to the initial structure.
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页数:8
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共 15 条
  • [1] The future of drug discovery and development: Shifting emphasis towards personalized medicine
    Amir-Aslani, Arsia
    Mangematin, Vincent
    [J]. TECHNOLOGICAL FORECASTING AND SOCIAL CHANGE, 2010, 77 (02) : 203 - 217
  • [2] Berthier J, 2010, ARTECH HSE INTEGR MI, P1
  • [3] The price of innovation: new estimates of drug development costs
    DiMasi, JA
    Hansen, RW
    Grabowski, HG
    [J]. JOURNAL OF HEALTH ECONOMICS, 2003, 22 (02) : 151 - 185
  • [4] Integrated microfluidic array plate (iMAP) for cellular and molecular analysis
    Dimov, Ivan K.
    Kijanka, Gregor
    Park, Younggeun
    Ducree, Jens
    Kang, Taewook
    Lee, Luke P.
    [J]. LAB ON A CHIP, 2011, 11 (16) : 2701 - 2710
  • [5] Apoptosis induced by different doses of caffeine on chinese hamster ovary cells
    Fernández, MJ
    López, A
    Santa-Maria, A
    [J]. JOURNAL OF APPLIED TOXICOLOGY, 2003, 23 (04) : 221 - 224
  • [6] The pressure drop along rectangular microchannels containing bubbles
    Fuerstman, Michael J.
    Lai, Ann
    Thurlow, Meghan E.
    Shevkoplyas, Sergey S.
    Stone, Howard A.
    Whitesides, George M.
    [J]. LAB ON A CHIP, 2007, 7 (11) : 1479 - 1489
  • [7] Transport and shear in a microfluidic membrane bilayer device for cell culture
    Inamdar, Niraj K.
    Griffith, Linda G.
    Borenstein, Jeffrey T.
    [J]. BIOMICROFLUIDICS, 2011, 5 (02):
  • [8] A practical guide to microfluidic perfusion culture of adherent mammalian cells
    Kim, Lily
    Toh, Yi-Chin
    Voldman, Joel
    Yu, Hanry
    [J]. LAB ON A CHIP, 2007, 7 (06) : 681 - 694
  • [9] Structured PDMS Chambers for Enhanced Human Neuronal Cell Activity on MEA Platforms
    Kreutzer, Joose
    Yla-Outinen, Laura
    Karna, Paula
    Kaarela, Tiina
    Mikkonen, Jarno
    Skottman, Heli
    Narkilahti, Susanna
    Kallio, Pasi
    [J]. JOURNAL OF BIONIC ENGINEERING, 2012, 9 (01) : 1 - 10
  • [10] Maki A., 2014, INT J HEAT MAS UNPUB