Biomedical Engineering Reference
In-Depth Information
7.4.1 Surface Properties
Wetability
Surface hydrophilicity/hydrophobicity of the biomaterials can be one of the
important parameters to regulate a series of cellular functions, including attach-
ment, migration, cytoskeletal organization, and differentiation [
181
]. Although it is
known that hydrophobic surface characteristics favor protein adsorption from the
aqueous surrounding solution, a hydrophilic surface is also necessary to initiate
cell attachment [
117
]. Therefore, controlling the optimum level of hydrophilicity/
hydrophobicity of the material surface could induce positive cell responses.
Technical methods to increase the hydrophilicity of hydrophobic synthetic poly-
meric biomaterials include grafting hydrophilic polymer through copolymerization
[
182
], plasma treatment to increase the number of oxygen-containing groups such
as -OH and -C=O [
183
,
184
], and photooxidation to introduce peroxide groups
onto the material surface with the aid of UV treatment [
117
]. For instance,
increasing hydrophilicity in copolymeric hydrogels by increasing the hydrophilic
PEG content relative to the hydrophobic PCL content resulted in higher prolif-
eration of primary rabbit chondrocytes [
182
]. In addition, more hydrophilic gels
(e.g., 14 wt% PEG and 6 wt% PCL) could be optimum to induce chondrogenic
differentiation, as determined by stimulated gene expression levels of type II
collagen, aggrecan, SOX9, and COMP. Plasma-treated electrospun PCL nanofibers
also
showed
higher
chondrocyte
adhesion
and
proliferation
than
untreated
hydrophobic PCL surfaces [
184
].
Roughness and Topography
Modulation of the hydrophilicity of the material surface can usually be related to
changes in topography and roughness [
181
,
184
-
186
]. Cell adhesion of both
human MSCs and porcine chondrocytes mediated by integrin b was influenced
by different topologies and surface roughness of PLGA-, PLA-, and PCL-coated
plates [
187
]. In addition to initial cell adhesion, topographical changes of the
material surface also affected chondrocyte aggregation (i.e., mesenchymal con-
densation) [
188
] and the osteoblastic signaling pathway [
186
]. Another study
using a composite bone scaffold also demonstrated the related changes in
increasing hydrophilicity and roughness by incorporation of hydroxyapatite
nanoparticles into a hydrophobic poly(propylene fumarate) scaffold [
185
]. In this
study, a mineral particle content of 20 wt% resulted in higher hydrophilicity and
roughness, and the changes in the physicochemical properties of the composite
material influenced osteogenic signal expression of rat bone marrow stromal
cells.
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