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载氟纳米羟基磷灰石多孔支架诱导牙髓干细胞成骨分化的研究。

On the osteogenic differentiation of dental pulp stem cells by a fabricated porous nano-hydroxyapatite substrate loaded with sodium fluoride.

机构信息

Department of Tissue Engineering and Applied Cell Sciences, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

出版信息

BMC Oral Health. 2024 Oct 14;24(1):1218. doi: 10.1186/s12903-024-04987-z.

Abstract

In the present study, nano-hydroxyapatite (n-HA) powder was extracted from carp bone waste to fabricate porous n-HA substrates by a molding and sintering process. Subsequently, the substrates were loaded with different amounts of sodium fluoride (NaF) through immersion in NaF suspensions for 10, 7.5, and 5 min. The NaF-loaded n-HA substrates were then examined for their structural and physical properties, chemical bonds, loading and release profile, pH changes, cytotoxicity, and osteogenic effect on dental pulp stem cells (DPSCs) at the level of RNA and protein expression. The results showed that the n-HA substrates were porous (> 40% porosity) and had rough surfaces. The NaF could be successfully loaded on the substrates, which was 6.43, 4.50, and 1.47 mg, respectively for n-HA substrates with immersion times of 10, 7.5, and 5 min in the NaF suspensions. It was observed that the NaF release rate was rather fast during the first 24 h in all groups (39.06%, 36.43%, and 39.57% for 10, 7.5, and 5 min, respectively), and decreased dramatically after that, indicating a slow detachment of NaF. Furthermore, the pH of the medium related to all materials was changed during the first 4 days of immersion (from 7.38 to pH of about 7.85, 7.84, 7.63, and 7.66 for C0, C5, C7.5, and C10, respectively). The pH of media associated with the C7.5, and C10 increased up to 4 days and remained relatively constant until day 14 (pH = 7.6). The results of the cytotoxicity assay rejected any toxicity of the fabricated NaF-loaded n-HA substrates on DPSCs, and the cells could adhere to their surfaces with enlarged morphology. The results showed no effect on the osteogenic differentiation at the protein level. Nevertheless, this effect was observed at the gene level.

摘要

在本研究中,从鲤鱼骨废料中提取纳米羟基磷灰石 (n-HA) 粉末,通过成型和烧结工艺制备多孔 n-HA 基质。随后,通过将基质浸入 NaF 悬浮液中 10、7.5 和 5 min,将不同量的氟化钠 (NaF) 负载到基质上。然后检查负载 NaF 的 n-HA 基质的结构和物理性质、化学键、负载和释放曲线、pH 值变化、细胞毒性以及对牙髓干细胞 (DPSCs) 的成骨作用在 RNA 和蛋白质表达水平。结果表明,n-HA 基质是多孔的(>40%的孔隙率)且表面粗糙。NaF 可以成功负载到基质上,分别为 10、7.5 和 5 min 浸泡在 NaF 悬浮液中的 n-HA 基质负载量为 6.43、4.50 和 1.47 mg。观察到在所有组中,NaF 释放率在最初的 24 小时内非常快(分别为 39.06%、36.43%和 39.57%),之后急剧下降,表明 NaF 的缓慢脱落。此外,与所有材料相关的介质的 pH 在浸泡的前 4 天内发生了变化(从 7.38 到 pH 约 7.85、7.84、7.63 和 7.66,分别为 C0、C5、C7.5 和 C10)。与 C7.5 和 C10 相关的介质的 pH 升高至 4 天,并在第 14 天之前保持相对稳定(pH = 7.6)。细胞毒性试验的结果排除了所制备的负载 NaF 的 n-HA 基质对 DPSCs 的任何毒性,并且细胞可以通过放大的形态附着在其表面上。结果表明在蛋白质水平上对成骨分化没有影响。然而,在基因水平上观察到了这种效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fd/11476061/52ac2948b84d/12903_2024_4987_Fig1_HTML.jpg

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