Structural connectivity and bioactivity in sol–gel silicate glass design

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL Acta Biomaterialia Pub Date : 2024-10-15 DOI:10.1016/j.actbio.2024.08.030
Chisokwuo Akunna, Marta Cerruti
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引用次数: 0

Abstract

Bioactive glasses (BGs) bond with bone by forming hydroxy carbonate apatite (HCA) upon reaction in physiological fluid, a phenomenon known as bioactivity. BGs structural network connectivity determines their bioactivity. Sol–gel BGs are synthesized through the hydrolysis and condensation of metal alkoxide precursors in the presence of a catalyst, in aqueous environments. Several sol–gel synthesis parameters directly impact BG network connectivity: pH (i.e. acid or basic catalysis), water to alkoxide ratio (Rw), alkoxide type and presence of dopant ions. However, the relationship between bioactivity and these parameters remains surprisingly unexplored.
This study highlights the relationship between synthesis pH, Rw, network connectivity and bioactivity in silica-based sol-gel BGs and BGs doped with titanium (Ti) ions (TiBGs), the latter selected for their known ability to enhance network connectivity. BGs and TiBGs are synthesized with various Rw values under acidic and basic conditions, and their bioactivity is assessed in simulated body fluid for 7 days.
Increasing Rw decreases network connectivity and increases bioactivity of BGs with high network connectivity, as observed for base-catalyzed BGs and for both acid and base catalyzed TiBGs, but not in BGs with lower connectivity as evidenced in acid-catalyzed BGs. Basic catalysis of TiBGs prevents crystalline TiO2 domain formation, which was instead consistently observed in TiBGs synthesized under acidic catalysis.
These findings help the design of BGs for applications where ion release needs to be enhanced even in the presence of dopants that slow down HCA formation, and of BGs with specific properties, e.g. TiO2-containing BGs with potential bactericidal activity.

Statement of significance

Bioactive glasses (BGs) bond with bone by dissolving and forming hydroxycarbonate apatite (HCA) on their surface, offering applications in medicine and dentistry. BG's network connectivity influences its dissolution rate, and hence HCA formation. While solution-gelation (sol-gel) is commonly used for BG production, the effect of sol gel synthesis parameters on HCA formation remains unexplored. We studied the relationship between synthesis parameters (water-to-alkoxide ratio (Rw), catalyst, and dopant ions, particularly titanium), BG network connectivity, and HCA formation. We find that increasing Rw with any catalyst enhances HCA formation, particularly in glasses with high network connectivity. This understanding allows tailoring BG synthesis for different applications, e.g. those requiring doping with ions that increase network connectivity and fills a crucial gap in BG literature.

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溶胶凝胶硅酸盐玻璃设计中的结构连接性和生物活性
生物活性玻璃(BGs)通过在生理液体中反应形成羟基碳酸盐磷灰石(HCA)而与骨骼结合,这种现象被称为生物活性。生物活性玻璃的结构网络连通性决定了其生物活性。溶胶-凝胶 BG 是在水环境中,在催化剂的作用下,通过水解和缩合金属氧化物前体合成的。有几个溶胶-凝胶合成参数会直接影响 BG 网络的连通性:pH 值(即酸性或碱性催化)、水与氧化烷比率 (Rw)、氧化烷类型和掺杂离子的存在。然而,生物活性与这些参数之间的关系却出人意料地尚未得到探讨。本研究强调了硅基溶胶凝胶 BGs 和掺杂钛(Ti)离子(TiBGs)的 BGs 的合成 pH 值、Rw 值、网络连通性和生物活性之间的关系。在酸性和碱性条件下合成了不同Rw值的BGs和TiBGs,并在模拟体液中对其生物活性进行了为期7天的评估。正如在碱催化的 BGs 以及酸和碱催化的 TiBGs 中观察到的那样,Rw 的增加会降低网络连通性并增加网络连通性高的 BGs 的生物活性,但在酸催化的 BGs 中却没有观察到网络连通性较低的 BGs 的生物活性。对 TiBGs 进行碱催化可阻止结晶 TiO2 结构域的形成,而在酸催化下合成的 TiBGs 中却能持续观察到这种结构域的形成。这些发现有助于设计应用于即使存在减缓 HCA 形成的掺杂剂也需要增强离子释放的 BGs,以及具有特殊性质的 BGs,例如具有潜在杀菌活性的含 TiO2 BGs。意义说明:生物活性玻璃(BGs)通过溶解并在其表面形成羟基碳酸盐磷灰石(HCA)与骨骼结合,可应用于医学和牙科领域。生物活性玻璃的网络连通性会影响其溶解速度,进而影响 HCA 的形成。虽然溶液凝胶法(溶胶-凝胶法)通常用于生产 BG,但溶胶凝胶合成参数对 HCA 形成的影响仍有待探索。我们研究了合成参数(水与氧化碱之比 (Rw)、催化剂和掺杂离子,尤其是钛)、BG 网络连通性和 HCA 形成之间的关系。我们发现,在使用任何催化剂的情况下,Rw 的增加都会促进 HCA 的形成,尤其是在具有高网络连通性的玻璃中。有了这一认识,我们就可以针对不同的应用领域(如需要掺杂能提高网络连通性的离子的应用领域)定制玻璃纤维合成方法,并填补了玻璃纤维文献中的一项重要空白。
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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
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