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Polystyrene surface was used as a reference.
Some types of cells, such as human umbilical vein endothelial cells (ECV304), proliferated with a viability rate similar to those on the polystyrene surface (Fig. 7c).
After 24 hours of all the seedings, the attached cells spread on both the hydrogel and the polystyrene surface in a morphologically comparable manner (Fig. 7a).
Overall, improved catalysis was observed for cellulase upon immobilization, especially to polystyrene surface.
Following tropoelastin attachment, cells spread preferentially on the PIII-treated sections of the polystyrene surface.
Smooth muscle cells grown on DegraPol® showed the same morphology as when grown on control polystyrene surface.
(a) The morphology of mouse myoblast cells (C2C12) growing on the polystyrene surface of the culture dishes (upper panel) and the sericin hydrogel (lower panel) at the different time points after seeding.
Once seeded on the sericin hydrogel, the cells started attaching to the hydrogel surface with the adhesion efficiency similar to the cells placed onto the polystyrene surface of culture dishes (Fig. 7a and b).
The images in scanning electron microscope showed that SWNHs on polystyrene surface are individual particles.
The blue colour bars represent the control (tissue culture treated polystyrene surface).
SEM micrographs of the untreated polystyrene surface are shown in Fig. 2a, b.
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