Characterization of a patch-clamp microchannel array towards neuronal networks analysis

Massimo Alberti, Detlef Snakenborg, Joanna M. Lopacinska, Martin Dufva, Jörg Peter Kutter

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    The attempt to combine the planar patch clamping idea with the microelectrode array (MEA) concept has led to the fabrication of a patch clamp micro-channel array (PC mu CA). Such a system is thought to be a powerful framework for neuroscience research and drug screening, as a novel tool for simultaneous patch clamping of cultured cells or neurons in the same network. A disposable silicon/silicon dioxide (Si/SiO2) chip with a microhole array was integrated in a microfluidic system for cell handling, perfusion and electrical recording. Fluidic characterization showed that our PC mu CA can work as a precise local perfusion system for chemicals or drugs. Electrical characterization for microholes of 2 mu m and 3 mu m revealed an access resistance of 8.09 +/- 0.84 M Omega and 3.18 +/- 0.63 M Omega, respectively. The capacitance was 98.6 +/- 13.2 pF. The values are close to what can be expected from theory, but the capacitance is still too high for high resolution recording. The system was tested on HeLa cells: successful cell trapping with a sealing of 40 M Omega was recorded. Modification of the Si/SiO2 chip is needed in order to achieve a better sealing and long-term cell culturing in the PC mu CA remains to be tested.
    Original languageEnglish
    JournalMicrofluidics and Nanofluidics
    Volume9
    Issue number4-5
    Pages (from-to)963-972
    ISSN1613-4982
    DOIs
    Publication statusPublished - 2010

    Keywords

    • Microchannel array
    • Perfusion
    • Cell detection
    • Neurochip
    • Electrochemical impedance spectroscopy
    • Patch clamp on a chip

    Cite this

    Alberti, Massimo ; Snakenborg, Detlef ; Lopacinska, Joanna M. ; Dufva, Martin ; Kutter, Jörg Peter. / Characterization of a patch-clamp microchannel array towards neuronal networks analysis. In: Microfluidics and Nanofluidics. 2010 ; Vol. 9, No. 4-5. pp. 963-972.
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    abstract = "The attempt to combine the planar patch clamping idea with the microelectrode array (MEA) concept has led to the fabrication of a patch clamp micro-channel array (PC mu CA). Such a system is thought to be a powerful framework for neuroscience research and drug screening, as a novel tool for simultaneous patch clamping of cultured cells or neurons in the same network. A disposable silicon/silicon dioxide (Si/SiO2) chip with a microhole array was integrated in a microfluidic system for cell handling, perfusion and electrical recording. Fluidic characterization showed that our PC mu CA can work as a precise local perfusion system for chemicals or drugs. Electrical characterization for microholes of 2 mu m and 3 mu m revealed an access resistance of 8.09 +/- 0.84 M Omega and 3.18 +/- 0.63 M Omega, respectively. The capacitance was 98.6 +/- 13.2 pF. The values are close to what can be expected from theory, but the capacitance is still too high for high resolution recording. The system was tested on HeLa cells: successful cell trapping with a sealing of 40 M Omega was recorded. Modification of the Si/SiO2 chip is needed in order to achieve a better sealing and long-term cell culturing in the PC mu CA remains to be tested.",
    keywords = "Microchannel array, Perfusion, Cell detection, Neurochip, Electrochemical impedance spectroscopy, Patch clamp on a chip",
    author = "Massimo Alberti and Detlef Snakenborg and Lopacinska, {Joanna M.} and Martin Dufva and Kutter, {J{\"o}rg Peter}",
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    Characterization of a patch-clamp microchannel array towards neuronal networks analysis. / Alberti, Massimo; Snakenborg, Detlef; Lopacinska, Joanna M.; Dufva, Martin; Kutter, Jörg Peter.

    In: Microfluidics and Nanofluidics, Vol. 9, No. 4-5, 2010, p. 963-972.

    Research output: Contribution to journalJournal articleResearchpeer-review

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    T1 - Characterization of a patch-clamp microchannel array towards neuronal networks analysis

    AU - Alberti, Massimo

    AU - Snakenborg, Detlef

    AU - Lopacinska, Joanna M.

    AU - Dufva, Martin

    AU - Kutter, Jörg Peter

    PY - 2010

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    N2 - The attempt to combine the planar patch clamping idea with the microelectrode array (MEA) concept has led to the fabrication of a patch clamp micro-channel array (PC mu CA). Such a system is thought to be a powerful framework for neuroscience research and drug screening, as a novel tool for simultaneous patch clamping of cultured cells or neurons in the same network. A disposable silicon/silicon dioxide (Si/SiO2) chip with a microhole array was integrated in a microfluidic system for cell handling, perfusion and electrical recording. Fluidic characterization showed that our PC mu CA can work as a precise local perfusion system for chemicals or drugs. Electrical characterization for microholes of 2 mu m and 3 mu m revealed an access resistance of 8.09 +/- 0.84 M Omega and 3.18 +/- 0.63 M Omega, respectively. The capacitance was 98.6 +/- 13.2 pF. The values are close to what can be expected from theory, but the capacitance is still too high for high resolution recording. The system was tested on HeLa cells: successful cell trapping with a sealing of 40 M Omega was recorded. Modification of the Si/SiO2 chip is needed in order to achieve a better sealing and long-term cell culturing in the PC mu CA remains to be tested.

    AB - The attempt to combine the planar patch clamping idea with the microelectrode array (MEA) concept has led to the fabrication of a patch clamp micro-channel array (PC mu CA). Such a system is thought to be a powerful framework for neuroscience research and drug screening, as a novel tool for simultaneous patch clamping of cultured cells or neurons in the same network. A disposable silicon/silicon dioxide (Si/SiO2) chip with a microhole array was integrated in a microfluidic system for cell handling, perfusion and electrical recording. Fluidic characterization showed that our PC mu CA can work as a precise local perfusion system for chemicals or drugs. Electrical characterization for microholes of 2 mu m and 3 mu m revealed an access resistance of 8.09 +/- 0.84 M Omega and 3.18 +/- 0.63 M Omega, respectively. The capacitance was 98.6 +/- 13.2 pF. The values are close to what can be expected from theory, but the capacitance is still too high for high resolution recording. The system was tested on HeLa cells: successful cell trapping with a sealing of 40 M Omega was recorded. Modification of the Si/SiO2 chip is needed in order to achieve a better sealing and long-term cell culturing in the PC mu CA remains to be tested.

    KW - Microchannel array

    KW - Perfusion

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    KW - Electrochemical impedance spectroscopy

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