The surfaces of standard untreated polystyrene cell culture dishes have bee
n oxidatively modified for up to 8 min exposure time using an ultraviolet o
zone treater in order to promote cell adhesion. Surface oxygen chemisorptio
n and topographical modification has been characterized using monochromatic
X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM),
respectively. The oxidation process is shown to proceed at low exposure tim
es (<60 s) via the formation of C-OR groups, although some R2C=O and RO-C=O
groups are also formed. At longer treatments, RO-C=O groups become the dom
inant species, although the other groups are also present. The maximum leve
l of oxygen reached is 36 atomic 8. Some of the oxygen present at surfaces
treated at times of >60 s is in the form of loosely bound low molecular wei
ght oxidized material (LMWOM) which is produced by oxidative scission of th
e PS backbone. Water washing leads to a reduction in surface oxygen content
mainly by the removal of RO-C=O and R2C=O functional groups. The residual
stable oxygen levels, which can be introduced, are approximately 20-25 atom
ic %. Surface chemistry changes are accompanied by the formation of surface
spikes which are about 30 nm high and 300-400 nm wide. A correlation betwe
en treatment time/oxygen level and overall roughness is observed. The effec
t of washing upon the topography is to slightly increase the surface roughn
ess, although not to a significant degree. The attachment kinetics of adhes
ion for Chinese hamster ovary cells show that adhesion occurs much more rap
idly for oxidized surfaces than for untreated control materials. A direct c
orrelation between the levels of oxidation and the rate of cell adhesion is
demonstrated.