Cardiovascular diseases
are a pre-eminent global cause
of mortality
in the modern world. Typically, surgical intervention with implantable
medical devices such as cardiovascular stents is
deployed to reinstate unobstructed blood flow. Unfortunately, existing
stent materials frequently induce restenosis and thrombosis, necessitating
the development of superior biomaterials. These biomaterials should
inhibit platelet adhesion (mitigating stent-induced thrombosis) and
smooth muscle cell proliferation (minimizing restenosis) while enhancing
endothelial cell proliferation at the same time. To optimize the surface
properties of Ti
6
Al
4
V medical implants, we investigated
two surface treatment procedures: gaseous plasma treatment and hydrothermal
treatment. We analyzed these modified surfaces through scanning electron
microscopy (SEM), water contact angle analysis (WCA), X-ray photoelectron
spectroscopy (XPS), and X-ray diffraction (XRD) analysis. Additionally,
we assessed in vitro biological responses, including platelet adhesion
and activation, as well as endothelial and smooth muscle cell proliferation.
Herein, we report the influence of pre/post oxygen plasma treatment
on titanium oxide layer formation via a hydrothermal technique. Our
results indicate that alterations in the titanium oxide layer and
surface nanotopography significantly influence cell interactions.
This work offers promising insights into designing multifunctional
biomaterial surfaces that selectively promote specific cell types’
proliferation—which is a crucial advancement in next-generation
vascular implants.