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研究富含白蛋白的富血小板纤维蛋白(Alb-PRF)的生物学功效:细胞因子动力学和成骨细胞行为研究。

Investigating the Biological Efficacy of Albumin-Enriched Platelet-Rich Fibrin (Alb-PRF): A Study on Cytokine Dynamics and Osteoblast Behavior.

机构信息

Clinical Research Unit, Antonio Pedro Hospital, Fluminense Federal University, Niteroi 24033-900, Brazil.

Graduate Program in Science and Biotechnology, Fluminense Federal University, Niteroi 24210-201, Brazil.

出版信息

Int J Mol Sci. 2024 Oct 27;25(21):11531. doi: 10.3390/ijms252111531.

DOI:10.3390/ijms252111531
PMID:39519084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11547010/
Abstract

The development of effective biomaterials for tissue regeneration has led to the exploration of blood derivatives such as leucocyte- and platelet-rich fibrin (L-PRF). A novel variant, Albumin-Enriched Platelet-Rich Fibrin (Alb-PRF), has been introduced to improve structural stability and bioactivity, making it a promising candidate for bone regeneration. This study aimed to evaluate Alb-PRF's capacity for cytokine and growth factor release, along with its effects on the proliferation, differentiation, and mineralization of human osteoblasts in vitro. Alb-PRF membranes were analyzed using histological, scanning electron microscopy, and fluorescence microscopy techniques. Cytokine and growth factor release was quantified over seven days, and osteoinductive potential was evaluated with MG-63 osteoblast-like cells. Structural analysis showed Alb-PRF as a biphasic, highly cellularized material that releases lower levels of inflammatory cytokines and higher concentrations of platelet-derived growth factor (PDGF) and vascular endothelial growth factor (VEGF) compared to L-PRF. Alb-PRF exhibited higher early alkaline phosphatase activity and in vitro mineralization ( < 0.05) and significantly increased the OPG/RANKL mRNA ratio ( < 0.05). These results indicate that Alb-PRF has promising potential as a scaffold for bone repair, warranting further in vivo and clinical assessments to confirm its suitability for clinical applications.

摘要

用于组织再生的有效生物材料的发展促使人们探索血液衍生物,如富含白细胞和血小板的纤维蛋白(L-PRF)。一种新型的变体,即富含白蛋白的血小板纤维蛋白(Alb-PRF),已被引入以提高结构稳定性和生物活性,使其成为骨再生的有前途的候选物。本研究旨在评估 Alb-PRF 释放细胞因子和生长因子的能力,以及其对体外人成骨细胞增殖、分化和矿化的影响。使用组织学、扫描电子显微镜和荧光显微镜技术分析 Alb-PRF 膜。在七天内定量测定细胞因子和生长因子的释放,并使用 MG-63 成骨样细胞评估成骨诱导潜力。结构分析表明,Alb-PRF 是一种双相的、高度细胞化的材料,与 L-PRF 相比,它释放较低水平的炎症细胞因子,较高浓度的血小板衍生生长因子(PDGF)和血管内皮生长因子(VEGF)。Alb-PRF 表现出更高的早期碱性磷酸酶活性和体外矿化(<0.05),并显著增加 OPG/RANKL mRNA 比值(<0.05)。这些结果表明,Alb-PRF 具有作为骨修复支架的巨大潜力,值得进一步进行体内和临床评估,以确认其在临床应用中的适用性。

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