含锂的 45S5 生物玻璃衍生玻璃陶瓷具有抗氧化活性,可诱导 1 型糖尿病大鼠临床前模型中新骨的形成。

Fátima Gomez Gramajo, María A Rivoira, Valeria Rodríguez, Gabriela Vargas, Rosa Vera Mesones, María P Zago, Aldo R Boccaccini, Alejandro Gorustovich
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摘要

糖尿病(DM)与影响骨骼系统的并发症有关,如骨修复改变、骨质疏松症和骨折风险增加。在这种情况下,使用能够促进成骨分化、同时限制糖尿病引起的氧化应激的生物材料,为确保糖尿病骨组织的修复提供了一个新的视角。由于锂(Li)最近被确认为一种具有成骨和抗氧化特性的生物活性离子,因此从生物活性玻璃陶瓷材料中局部可控释放锂离子是治疗糖尿病骨损伤的一种很有前景的治疗方法。因此,本研究的目的是在 1 型 DM(DM1)的实验模型中,评估 45S5 型生物活性玻璃(Bioglass)衍生出的玻璃陶瓷微粒的潜在成骨和抗氧化作用,这种玻璃陶瓷微粒含有(重量百分比)45% SiO2、24.5% Na2O、24.5% CaO 和 6%P2O5,其中 Na2O 部分被 5%的 Li2O(45S5.5Li)替代。研究结果首次证明,45S5 和 45S5.5Li 玻璃陶瓷微粒都具有抗氧化活性,无论是在生理条件下还是在实验性 DM1 大鼠体内,它们都能刺激活体骨形成。从这个意义上说,它们有可能作为无机成骨剂应用于不同的骨组织再生医学策略中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lithium-containing 45S5 Bioglass-derived glass-ceramics have antioxidant activity and induce new bone formation in a rat preclinical model of type 1 diabetes mellitus.

Diabetes mellitus (DM) has been associated with complications that affect the skeletal system, such as alterations in bone repair, osteoporosis, and an increased risk of fractures. In this context, the use of biomaterials able to promote osteogenic differentiation and, at the same time, limit the oxidative stress induced by DM offers a novel perspective to ensure the repair of diabetic bone tissue. Since lithium (Li) has been recently identified as a biologically active ion with osteogenic and antioxidant properties, the localized and controlled release of Li ions from bioactive glass-ceramic materials represents a promising therapeutic alternative for the treatment of bone lesions in DM. Thus, the aim of this study was to evaluate the potential osteogenic and antioxidant effects of glass-ceramic microparticles derived from a 45S5-type bioactive glass (Bioglass) containing (% by weight) 45% SiO2, 24.5% Na2O, 24.5% CaO, and 6% P2O5, in which Na2O was partially substituted by 5% of Li2O (45S5.5Li), in an experimental model of type 1 DM (DM1). The results obtained demonstrate, for the first time, that both 45S5 and 45S5.5Li glass-ceramic microparticles possess antioxidant activity and stimulate bone formationin vivoboth under physiological conditions and under experimental DM1 in rats. In this sense, they would have potential application as inorganic osteogenic agents in different strategies of bone tissue regenerative medicine.

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