加入骨基质颗粒的光交联水凝胶,促进牙本质组织工程的发展。

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Isabela Sanches Pompeo da Silva, Ester Alves Ferreira Bordini, Erika Soares Bronze-Uhle, Vitor de Stuani, Matheus Castro Costa, Letícia Alves Martins de Carvalho, Fernanda Balestrero Cassiano, Lucas José de Azevedo Silva, Ana Flávia Sanches Borges, Diana Gabriela Soares
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引用次数: 0

摘要

本研究的目的是使用明胶甲基丙烯酰(GelMA)水凝胶,结合脱细胞骨基质(BMdc)和去蛋白牛骨基质(BMdp),制作可注射的光交联生物材料。这些材料可用作牙本质再生的生物活性支架。首先选定 GelMA 水凝胶的制造参数,然后以 1%(w/v)的比例加入 BMdc 和 BMdp。纳米羟基磷灰石(nHA)也作为对照。傅立叶变换红外分析表明,矿物相与 GelMA 复合,BMdc 与明胶的酰胺基发生化学键合。在加入 BMdc 后,多孔结构得以保留,骨颗粒与孔隙融为一体。相反,矿物相位于孔隙开口内,影响了孔隙度。即使在 I 型胶原酶介导的酶促条件下,矿物相也不会改变 GelMA 的降解性,从而允许水凝胶注入并增加机械强度。随后,人类牙髓细胞(HDPCs)被播种到水凝胶上。无论 GelMA 的成分如何,细胞都能保持活力和增殖。所有矿物相都能显著提高碱性磷酸酶活性和矿化基质沉积。然而,GelMA-BMdc 表现出更高的细胞表达值,明显超过所有其他配方。总之,我们的研究结果表明,GelMA-BMdc 产生了一种多孔且稳定的水凝胶,在与 HDPCs 接触时能够促进牙本质分化和矿物质沉积,从而显示出牙本质再生的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photo-crosslinkable hydrogel incorporated with bone matrix particles for advancements in dentin tissue engineering

The objective of this study was to create injectable photo-crosslinkable biomaterials, using gelatin methacryloyl (GelMA) hydrogel, combined with a decellularized bone matrix (BMdc) and a deproteinized (BMdp) bovine bone matrix. These were intended to serve as bioactive scaffolds for dentin regeneration. The parameters for GelMA hydrogel fabrication were initially selected, followed by the incorporation of BMdc and BMdp at a 1% (w/v) ratio. Nano-hydroxyapatite (nHA) was also included as a control. A physicochemical characterization was conducted, with FTIR analysis indicating that the mineral phase was complexed with GelMA, and BMdc was chemically bonded to the amide groups of gelatin. The porous structure was preserved post-BMdc incorporation, with bone particles incorporated alongside the pores. Conversely, the mineral phase was situated inside the pore opening, affecting the degree of porosity. The mineral phase did not modify the degradability of GelMA, even under conditions of type I collagenase-mediated enzymatic challenge, allowing hydrogel injection and increased mechanical strength. Subsequently, human dental pulp cells (HDPCs) were seeded onto the hydrogels. The cells remained viable and proliferative, irrespective of the GelMA composition. All mineral phases resulted in a significant increase in alkaline phosphatase activity and mineralized matrix deposition. However, GelMA-BMdc exhibited higher cell expression values, significantly surpassing those of all other formulations. In conclusion, our results showed that GelMA-BMdc produced a porous and stable hydrogel, capable of enhancing odontoblastic differentiation and mineral deposition when in contact with HDPCs, thereby showing potential for dentin regeneration.

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来源期刊
Journal of biomedical materials research. Part A
Journal of biomedical materials research. Part A 工程技术-材料科学:生物材料
CiteScore
10.40
自引率
2.00%
发文量
135
审稿时长
3.6 months
期刊介绍: The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device. The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.
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