一种含有羟基磷灰石、壳聚糖、黄原胶和氧化石墨烯的骨替代生物材料,辅以间充质干细胞条件培养基,实现骨再生。

Daniel N Rocha, David Gm López, José Rm Ferreira, Marcelo Hp Silva, Isabela Aaap Filgueiras, Bruno F Alves, Bruno M Almeida, Tatiana Kotaka, Leonardo F Buss, Marcelo L Teixeira, Éric D Mariano, Mariáh H Cationi, Isadora Bosco, Marvin Nascimento, Raul Canal, José G Neves, Antonio C Aloise, Elizabeth F Martinez, Lexie S Holliday, André A Pelegrine
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引用次数: 0

摘要

本研究分析了最近开发的一种由壳聚糖-黄原羟基磷灰石-氧化石墨烯(CXHAG)制成的骨替代生物材料。对 CXHAG 颗粒进行了体外结构和形态表征,并在体内与间充质干细胞成骨条件培养基或不与间充质干细胞成骨条件培养基混合进行了测试。目的:本研究旨在确定 CXHAG 新型生物材料在补充间充质干细胞条件培养基后能否用于骨再生。材料与方法:在体外研究中,细胞与 20 毫克的 CXHAG 颗粒培养 24 小时,并进行 MTT 试验以检测细胞毒性。在体内研究中,对 25 只大鼠进行了临界大小的腓骨缺损。一只大鼠的缺损未被填充(对照组-CG),42 天后安乐死。十二只大鼠接受了 CXHAG 颗粒(1-G1 组),另外十二只接受了补充了条件培养基的 CXHAG 颗粒(2-G2 组)。所有 G1/G2 移植物都覆盖有一层 CXHAG 膜。G1/G2 动物在 14 天(T1)或 42 天(T2)后安乐死。对标本进行处理和组织学评估。结果CXHAG 颗粒的扫描电镜分析显示,颗粒大小为 300-400μm,表面粗糙不规则。它们在体外对牙髓干细胞没有细胞毒性。CG 标本显示出松散的未成熟结缔组织,缺损中心没有骨形成。G1 和 G2 在两个时间点都出现了残余生物材料颗粒,但只有 G2 在缺损中心有骨形成。结论:当条件培养基与新型骨替代生物材料结合使用时,对大鼠腓骨临界大小缺损的骨再生有积极作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bone regeneration by a bone substitute biomaterial containing hydroxyapatite, chitosan, xanthan and graphene oxide supplemented with conditioned medium from mesenchymal stem cells.

This study analyzed a recently developed bone substitute biomaterial made of chitosan-xanthanhydroxyapatite-graphene oxide (CXHAG). The CXHAG particles underwent in vitro structural and morphological characterization, and in vivo testing with or without osteogenic conditioned medium from mesenchymal stem cells. Aim: The aim of this study was to determine whether the CXHAG novel biomaterial, supplemented with conditioned medium from mesenchymal stem cells, could be useful for bone regeneration. Materials and Method: For the in vitro study, cells were incubated with 20mg of CXHAG granules for 24 hours and a MTT assay was performed to tests for cytotoxicity. For the in vivo study, critical size calvarial bone defects were created in twenty-five rats. One animal had the defect unfilled (Control Group-CG) and was euthanized after 42 days. Twelve rats received the CXHAG particles (Group 1-G1) and the other twelve received the CXHAG particles supplemented with the conditioned medium (Group 2-G2). All G1/G2 grafts were covered with a CXHAG membrane. G1/G2 animals were euthanized after 14 days (T1) or 42 days (T2). The specimens were processed and histologically evaluated. Results: SEM analysis of the CXHAG particles showed granules of 300-400μm, with a rough irregular surface. They were not cytotoxic to dental pulp stem cells in vitro. The CG specimen showed loose immature connective tissue and no bone formation at the center of the defect. G1 and G2 presented remnant biomaterial particles at both time points, but only G2 had bone formation at the enter of the defect. Conclusions: The conditioned medium had a positive effect on bone regeneration in rat calvarial critical size defects when associated with the novel bone substitute biomaterial.

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