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含羟基磷灰石、壳聚糖、黄原胶和氧化石墨烯的骨替代生物材料通过间充质干细胞条件培养基促进骨再生。

Bone regeneration by a bone substitute biomaterial containing hydroxyapatite, chitosan, xanthan and graphene oxide supplemented with conditioned medium from mesenchymal stem cells.

机构信息

Department of Bioengineering, R-Crio Criogenia S.A., Campinas, Brazil.

Department of Materials Engineering-SE/8, Military Institute of Engineering, Rio de Janeiro, Brazil.

出版信息

Acta Odontol Latinoam. 2024 Sep 30;37(2):151-161. doi: 10.54589/aol.37/2/151.

DOI:10.54589/aol.37/2/151
PMID:39484748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11590008/
Abstract

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.

摘要

本研究分析了一种最近开发的壳聚糖-黄原胶-羟基磷灰石-氧化石墨烯(CXHAG)复合骨替代生物材料。对 CXHAG 颗粒进行了体外结构和形态学特征分析,并在有无间充质干细胞成骨条件培养基的情况下进行了体内测试。目的:本研究旨在确定新型生物材料 CXHAG 补充间充质干细胞条件培养基是否可用于骨再生。材料和方法:在体外研究中,将细胞与 20mg 的 CXHAG 颗粒共培养 24 小时,然后进行 MTT 测定以测试细胞毒性。在体内研究中,在 25 只大鼠的颅骨临界尺寸骨缺损中进行了实验。一只动物的缺损未填充(对照组-CG),并在 42 天后安乐死。12 只大鼠接受 CXHAG 颗粒(第 1 组-G1),另 12 只大鼠接受补充有条件培养基的 CXHAG 颗粒(第 2 组-G2)。所有 G1/G2 移植物均覆盖 CXHAG 膜。G1/G2 动物在 14 天(T1)或 42 天(T2)时安乐死。对标本进行处理和组织学评估。结果:SEM 分析显示 CXHAG 颗粒为 300-400μm 的颗粒,表面粗糙不规则。它们在体外对牙髓干细胞无细胞毒性。CG 标本显示中心缺损处松散的未成熟结缔组织和无骨形成。G1 和 G2 在两个时间点均存在残留生物材料颗粒,但只有 G2 在缺损中心有骨形成。结论:当新型骨替代生物材料与成骨条件培养基联合使用时,对大鼠颅骨临界尺寸缺损中的骨再生具有积极作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/96597c66b337/1852-4834-37-2-151-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/0e520826c33a/1852-4834-37-2-151-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/44c01e89eff9/1852-4834-37-2-151-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/49f920a1aa55/1852-4834-37-2-151-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/dfac7933f1ac/1852-4834-37-2-151-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/8d4ef23b3fe0/1852-4834-37-2-151-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/96597c66b337/1852-4834-37-2-151-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/0e520826c33a/1852-4834-37-2-151-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/44c01e89eff9/1852-4834-37-2-151-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/49f920a1aa55/1852-4834-37-2-151-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/dfac7933f1ac/1852-4834-37-2-151-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/8d4ef23b3fe0/1852-4834-37-2-151-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3968/11590008/96597c66b337/1852-4834-37-2-151-g007.jpg

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