Barbieri Thesis - BioMedical Materials program (BMM)
Barbieri Thesis - BioMedical Materials program (BMM)
Barbieri Thesis - BioMedical Materials program (BMM)
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Chapter 5 – Alkali surface treatment effects<br />
This conclusion is strengthened by their similar in vitro degradation, mineralization<br />
trends and serum protein adsorption (§5.3.3., §5.3.4. and §5.3.5.), indicating that no<br />
other factors than surface roughness were involved in inducing the different cellular<br />
performances.<br />
In this study, the failure of the in vitro model to predict the in vivo performance of<br />
composites indicates that, in biomaterials science, extrapolating in vitro biological<br />
results (e.g. cell culture or protein adsorption) into in vivo performances is a complex<br />
issue. In vitro models reduce the intrinsic variability present in living bodies simplifying<br />
the system. For example, as mentioned in §5.2.8., in this study we decided to culture<br />
cells onto discs to avoid cell seeding and nutritional inhomogeneities usually<br />
associated to three–dimensional systems such as (porous) granules. Further, when a<br />
material is placed in cell culture, it enters in contact with a closed system having<br />
culture medium and its composition (i.e. proteins, nutrients) carefully chosen where<br />
pH, carbon dioxide concentration and temperature are strictly stabilized. Besides this,<br />
cells are chosen and no other undesired lines or organisms are present to interfere<br />
with the used ones. On the contrary, if the same material is placed in the body, many<br />
factors that are not included in an in vitro culture system play roles on the overall<br />
performance of the material. For example, inflammation and foreign body reaction<br />
attract other forms of cells such as monocytes and macrophages which then release<br />
cytokines further recruiting other kinds of cell. [217, 256, 257] During this reaction, the<br />
material may degrade due to phagocytosis [375] and may change its properties affecting<br />
on its own performance. Further, body fluids have more heterogeneous composition<br />
than culture medium rendering the in vivo interaction between cells and materials<br />
surface more complex than in vitro.<br />
However, in this study we demonstrated that alkali treating the surface of the<br />
composite with sodium hydroxide solutions generated differently disordered nano–<br />
rough surfaces. In particular, the stronger treatment led to topographically disordered<br />
surfaces with higher roughness (Figures 3 and 4, Table 5). The enhanced surface<br />
nano–structure is likely caused by the hydrolysis of the polymer matrix [366] and by the<br />
consequent larger exposure of apatite on the surface (as shown by thicker apatite<br />
layers surrounding M1 and M2, Figure 2). The water contact angle of the composites<br />
diminished with the strength of the surface treatment indicating an increase of their<br />
polar character. This may be partially caused by the formation and exposure of polar<br />
groups due to the polymer hydrolysis provoked by the alkaline treatment, [366] and<br />
partly by the exposure of larger amount of hydrophilic apatite.<br />
The composites degraded over three months as indicated by their mass loss (Table<br />
6), which resulted similar with each other. However, higher concentrations of calcium<br />
and phosphate ions in SPS containing M1 and M2 as compared to M0 were observed<br />
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