Loading…
Displacement Talbot lithography nanopatterned microsieve array for directional neuronal network formation in brain-on-chip
Commercial microelectrode arrays (MEAs) for in vitro neuroelectrophysiology studies rely on conventional two dimensional (2D) neuronal cultures that are seeded on the planar surface of such MEAs and thus form a random neuronal network. The cells attaching on these types of surfaces grow in 2D and lo...
Saved in:
Published in: | Journal of vacuum science and technology. B, Nanotechnology & microelectronics Nanotechnology & microelectronics, 2016-11, Vol.34 (6) |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Commercial microelectrode arrays (MEAs) for in vitro
neuroelectrophysiology studies rely on conventional two dimensional (2D) neuronal cultures
that are seeded on the planar surface of such MEAs and thus form a random neuronal network. The
cells
attaching on these types of surfaces grow in 2D and lose their native morphology, which
may also influence their neuroelectrical behavior. Besides, a random neuronal network formed on this
planar surface in vitro also lacks comparison to the in
vivo state of brain tissue. In order to improve the present MEA platform with
the above mentioned concerns, in this paper, the authors introduce a three dimensional
platform for neuronal cell culturing, where a linear nanoscaffold is patterned on a
microsieve array by displacement Talbot lithography (DTL) and reactive ion etching. Good
pattern
uniformity is achieved by the DTL method on the topographically prepatterned nonflat
surface of the microsieve array. Primary cortical cells cultured on the
nanopatterned microsieve array show an organized network due to the contact
guidance provided by the nanoscaffold, presenting 47% of the total outgrowths aligning
with the nanogrooves in the observed view of field. Hence, the authors state that this
nanopatterned microsieve array can be further integrated into microsieve-based
microelectrode arrays to realize an advanced Brain-on-Chip model that allows us to
investigate the neurophysiology of cultured neuronal networks with specifically organized
architectures. |
---|---|
ISSN: | 2166-2746 2166-2754 |
DOI: | 10.1116/1.4961591 |