Table 1.
substrate | contact angle measurement(degree)c,f | cell adhesion(cells/cm2)d,f | cell detachment e | |
---|---|---|---|---|
25 °C | 37 °C | |||
plain PS | 77.6 ± 1.9 | 69.6 ± 1.1 | (5.1 ± 4.3) × 10 3 | No |
densely-packed PNIPAM microgels on PS a | 39.6 ± 3.7 | 41.6 ± 3.9! | (6.6 ± 4.5) × 10 3 | Yes |
sparsely-distributed PNIPAM microgels on PS b | 60.3 ± 2.8 | 61.6 ± 1.4 | (20.7 ± 11.4) × 10 3* | Yes |
50 μm stripes/50 μm spacings | 45.5 ± 3.9 | 42.8± 4.0 | (29.2 ± 8.0) × 10 3* | Yes |
50 μm stripes/100 μm spacings | 38.8 ± 2.7 | 41.7 ± 3.0 | (12.9 ± 5.0) × 10 3* | Yes |
100 μm stripes/100 μm spacings | 43.7 ±1.1 | 39.7 ± 1.6 | (15.4 ± 3.2) ×10 3* | Yes!! |
PS substrate dip coated with PNIPAM microgels at the withdrawal rate of 90 μm/min.
PS substrate dip coated with PNIPAM microgels at the withdwaral rate of 50.9 mm/min.
Static water contact angle using the captive bubble method. Measurements were conducted at ambient temperature (24.5 °C) or 37 °C by heating the chamber with a heating strip.
Cells were seeded on samples at 12000 cells/cm2 and incubated at 37 °C for 24 hours. These substrates were imaged using DIC and cell adhesion per unit area was calculated from at least 10 different optical micrographs using 3 different substrates per condition.
Cell detachment was performed by washing the substrate with tissue culture media at 25 °C.
Data represents mean ± st dev.
p<0.05 vs plain PS.