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Structural characterisation of hypoxia-mimicking bioactive glasses
Jodie M Smith1, Richard A Martin, Gabriel J Cuello
1School of Physical Sciences, University of Kent, Ingram Building, Canterbury, CT2 7NH, UK.
Journal of Materials Chemistry. B
|April 9, 2020
Summary
Nickel and cobalt in bioactive glasses stimulate blood vessel formation by releasing ions. These elements integrate into the glass structure without altering bioactivity, crucial for tissue engineering.
Area of Science:
- Biomaterials Science
- Materials Chemistry
- Tissue Engineering
Background:
- Nickel and cobalt ions stimulate hypoxia-inducible factor-1 (HIF-1α).
- HIF-1α activation promotes blood vessel formation, essential for tissue engineering.
- Bioactive glasses can serve as controlled delivery systems for therapeutic ions.
Purpose of the Study:
- To investigate the structural role of nickel (Ni) and cobalt (Co) in doped bioactive glasses.
- To understand how Ni and Co incorporation affects the glass structure and its properties.
- To correlate structural findings with potential bioactivity and ion release.
Main Methods:
- Neutron diffraction with isotopic and isomorphic substitution was employed.
- Structural analysis focused on the coordination environments of Ni and Co ions.
- Comparison of structural parameters with archetypal 45S5 Bioglass®.
Main Results:
- Nickel and cobalt ions occupy mixed structural sites: two-thirds in a five-fold coordination (network-modifying) and one-third in a tetrahedral coordination (network-forming).
- No significant differences were observed in primary structural correlations (e.g., Si-O, Ca-O) compared to 45S5 Bioglass®.
- The incorporation of Ni or Co does not adversely affect the fundamental glass structure.
Conclusions:
- Nickel and cobalt integrate into bioactive glasses in specific coordination geometries.
- The structural integrity of the bioactive glass is maintained upon Ni and Co doping.
- These findings suggest that Ni- and Co-doped bioactive glasses retain their bioactivity and dissolution properties for controlled ion delivery in tissue engineering.
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