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3D打印的缺钙羟基磷灰石/胶原蛋白/骨形态发生蛋白2支架促进大鼠颅骨缺损的愈合

Enhanced healing of rat calvarial defects with 3D printed calcium-deficient hydroxyapatite/collagen/bone morphogenetic protein 2 scaffolds.

作者信息

Han Shi Huan, Lee JiUn, Lee Kyung Mee, Jin Yuan Zhe, Yun Hui-Suk, Kim GeunHyung, Lee Jae Hyup

机构信息

Department of Orthopedic Surgery, College of Medicine, Seoul National University, Seoul, 03080, South Korea; Department of Orthopedic Surgery, YanBian University Hospital, 133000, Yanji, Jilin Province, China.

Department of Biomechatronic Engineering, College of Biotechnology and Bioengineering, Sungkyunkwan University (SKKU), Suwon, South Korea.

出版信息

J Mech Behav Biomed Mater. 2020 Aug;108:103782. doi: 10.1016/j.jmbbm.2020.103782. Epub 2020 Apr 16.

DOI:10.1016/j.jmbbm.2020.103782
PMID:32469715
Abstract

In this paper, we mainly to evaluate the newly formed bone using the Calcium deficient hydroxyapatite (CDHA)/collagen-based bio-ceramic scaffold as Bone Morphogenetic Protein-2 (BMP-2) carrier in rat calvarial critical-sized bone defect. In the real-time PCR analysis, the CDHA/collagen scaffold loaded rhBMP-2 group showed significantly enhanced results of bone-related gene expression (p < 0.05). In the in vivo study, the micro-CT showed that the main bone formation parameters of percent bone volume and trabecular number of the two experiment groups (CDHA/Collagen (CDHA) group, BV/TV: 14.21 ± 3.20, Tb.N: 2.37 ± 0.50; CDHA/Collagen/rhBMP-2(BMP) group, BV/TV: 14.51 ± 3.12, Tb.N: 2.75 ± 0.65) were significantly higher than those of the control (Blank, BV/TV: 3.25 ± 1.25, Tb.N: 0.57 ± 0.20) group (p < 0.05). Although there was no significant difference between the two experimental groups, the BMP group results were slightly higher than those of the CDHA group (p > 0.05). Moreover, the histological results also supported the micro-CT results. The scaffold of CDHA/collagen seems to be a suitable bio-ceramic carrier loaded rhBMP-2, and appears to enhance new bone formation and bone regeneration in bone defect after implantation.

摘要

在本文中,我们主要评估了使用缺钙羟基磷灰石(CDHA)/胶原蛋白基生物陶瓷支架作为骨形态发生蛋白-2(BMP-2)载体修复大鼠颅骨临界尺寸骨缺损时新形成的骨组织。在实时聚合酶链反应分析中,负载重组人骨形态发生蛋白-2(rhBMP-2)的CDHA/胶原蛋白支架组显示骨相关基因表达结果显著增强(p < 0.05)。在体内研究中,显微计算机断层扫描(micro-CT)显示,两个实验组(CDHA/胶原蛋白(CDHA)组,骨体积百分比:14.21±3.20,骨小梁数量:2.37±0.50;CDHA/胶原蛋白/rhBMP-2(BMP)组,骨体积百分比:14.51±3.12,骨小梁数量:2.75±0.65)的主要骨形成参数显著高于对照组(空白组,骨体积百分比:3.25±1.25,骨小梁数量:0.57±0.20)(p < 0.05)。虽然两个实验组之间没有显著差异,但BMP组的结果略高于CDHA组(p > 0.05)。此外,组织学结果也支持了micro-CT结果。CDHA/胶原蛋白支架似乎是一种适合负载rhBMP-2的生物陶瓷载体,并且在植入后似乎能促进骨缺损处的新骨形成和骨再生。

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