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Techniques for patterning and guidance of primary culture neurons on micro-electrode arrays

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TLDR
Two different micro-patterning methods for use in the growth guidance of dissociated primary culture neuron cells are compared: open chemically patterned growth substrates and enclosed micro-fluidic channels.
Abstract
In this work, two different micro-patterning methods for use in the growth guidance of dissociated primary culture neuron cells are compared: open chemically patterned growth substrates and enclosed micro-fluidic channels. Open, chemically patterned growth substrates are prepared by photolithographically patterning perfluoropolymer barrier structures on glass substrates. Neural pathways are created when poly- l -lysine is selectively adsorbed on the glass to form a cytophilic growth matrix. Adsorption of albumin proteins on the perfluoropolymer regions renders the surface cytophobic. In a second method, a three-dimensional micro-fluidic system, fabricated from PDMS is tested as a way to guide neural growth through total confinement and for cell placement. Both of these methods are tested for alignment and compatibility on a commercially available micro-electrode array (MED64). Biological culture and imaging techniques are considered.

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Citations
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Methods for Fabrication of Nanoscale Topography for Tissue Engineering Scaffolds

TL;DR: A number of techniques are currently being used to create nanoscale topographies for cell scaffolding, which fall into two main categories: techniques that create ordered topographies and those that create unordered topographies.
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PDMS 2D optical lens integrated with microfluidic channels: principle and characterization.

TL;DR: It is shown that the beam properties of the light coming out from the fiber can be modified depending on the lens curvature radius, and this excitation improvement corresponding to a stronger response from the dye leads to around three times higher sensitivity of the on-chip detection method for fluorescent spectroscopy.
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Biology on a chip: microfabrication for studying the behavior of cultured cells.

TL;DR: Here, microtechnology is conceptually well suited for the development of fast, low-cost in vitro systems that allow for high-throughput culturing and analysis of cells under large numbers of conditions.
Journal ArticleDOI

Constraining the connectivity of neuronal networks cultured on microelectrode arrays with microfluidic techniques: a step towards neuron-based functional chips.

TL;DR: Three-dimensional microfluidic systems in poly(dimethylsiloxane) (PDMS) were fabricated and used in conjunction with both custom-made and commercially available planar microelectrode arrays (pMEAs) to address the problem of in vitro culture of small neuronal networks with pre-defined topological features.
References
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Journal ArticleDOI

Controlled outgrowth of dissociated neurons on patterned substrates

TL;DR: A set of procedures for patterning the outgrowth of cells cultured on 2-dimensional substrates showed that glia are patterned along with the associated granule cells, and Interestingly, the GFAP-positive glia that proliferated on surfaces bound with amine derivatives attained primarily a tile-shaped, fibroblast-like morphology, while those proliferating on glass coated with poly(D-lysine) developed primarily a spindle- shaped, process-bearing morphology.
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The neurochip: a new multielectrode device for stimulating and recording from cultured neurons.

TL;DR: It is demonstrated that this device is capable of maintaining cell survival, and that the electrodes can both record and stimulate electrical activity in individual cells with no crosstalk between channels.
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A new planar multielectrode array for extracellular recording application to hippocampal acute slice

TL;DR: A new planar multielectrode array (the MED probe) and its electronics which perform electrophysiological studies on acute hippocampal slices and a spatial distribution of long-term potentiation was studied using the MED system.
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Silicon-Neuron Junction: Capacitive Stimulation of an Individual Neuron on a Silicon Chip.

TL;DR: The integration of electronic circuitry and neuronal networks requires a bidirectional electrical communication between silicon elements and nerve cells and the successful assembly of a neuron-to-silicon junction is reported with direct signal transfer from an individual neuron to a microscopic metal-free fieldeffect transistor.
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Microelectrode Array Recordings of Patterned Hippocampal Neurons for Four Weeks

TL;DR: Recordable, extracellular electrical activity began as early as 6 days in vitro and continued for the duration of the culture, consistent with results from unpatterned culture technologies.
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