Rapid Communications
FIG. 5. SEM of ring pattern: (a) top surface; (b) edge; (c) top surface near edge; (d) pattern edge.
the “low density dots” template [pattern Fig. 2(b)] shows
culture substrata. For example, we recently investigated
the influence of substrate surface structure on epithelial
cell adhesion and spreading using the described tech-
nique.17 We were able to show that cellular responses to
surface topography depend both on cell phenotype and
microtexture of the surface in the absence of extracellular
matrix proteins. In other reports, a high-resolution printer
was shown capable of generating 20 m patterns with
good quality.11,18,19 Such resolution18 is sufficient for
many applications in biotechnology and tissue engineer-
ing where the ability to fabricate confined areas of mi-
cron scale surface roughness is desired. On the other
hand, the major advantages of the method are its very
low cost, versatility, ease of use, rapid turnaround time,
and pattern resolution and roughness suitable for the pro-
duction of substrates for cell growth and bioassays.
a surface topography that consists of a lattice structure
with a average height of 7 m, width of 380 m, a pat-
tern surface roughness of 2.5 m, and a transparency
surface roughness of 10 nm. These templates produced in
the replicas an array of microwells [Fig. 6(b)] separated
by 290 m borders of unpatterned PDMS with nanoscale
surface roughness similar to the transparency films. The
“high density dot” templates [Fig. 2(c)] and replicas
were very similar except that slightly deeper micro-
wells were produced (8 m) with mean bottom surface
roughness of 2 m and top (unpatterned surface) rough-
ness of 5 nm.
In conclusion, we demonstrated a practical method for
rapid production of replica molding templates using laser
printer transparencies as templates for soft lithography.
This method requires no specialized microlithographic
equipment or cleanroom facilities. The PDMS replicas
directly cast on the laser printed templates accurately
reproduce the laser printer resolution and pattern surface
topography. The major disadvantages of the present
method are a poor resolution and a lack of control over
the depth of the patterns. However, this is a useful tech-
nique to generate microstructures with a resolution ap-
propriate for use in bioanalytical devices or as cell
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FIG. 6. Bright-field micrograph of the PDMS replica taken from the
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J. Mater. Res., Vol. 17, No. 7, Jul 2002
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