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本文引用的文献

1
Biomimetic apatite-coated alginate/chitosan microparticles as osteogenic protein carriers.仿生磷灰石涂层海藻酸盐/壳聚糖微粒作为成骨蛋白载体
Biomaterials. 2009 Oct;30(30):6094-101. doi: 10.1016/j.biomaterials.2009.07.046. Epub 2009 Aug 11.
2
Porous beta tricalcium phosphate scaffolds used as a BMP-2 delivery system for bone tissue engineering.多孔 β-磷酸三钙支架作为骨组织工程中的 BMP-2 递送系统。
J Biomed Mater Res A. 2010 Mar 1;92(3):1105-14. doi: 10.1002/jbm.a.32467.
3
A porcine collagen-derived matrix as a carrier for recombinant human bone morphogenetic protein-2 enhances spinal fusion in rats.一种源自猪胶原蛋白的基质作为重组人骨形态发生蛋白-2的载体可增强大鼠的脊柱融合。
Spine J. 2009 Jan-Feb;9(1):22-30. doi: 10.1016/j.spinee.2008.08.009. Epub 2008 Sep 19.
4
In vitro stability of lyophilized and reconstituted recombinant activated factor VII formulated for storage at room temperature.冻干并复溶后的重组活化凝血因子 VII 在室温储存条件下的体外稳定性。
Clin Ther. 2008 Jul;30(7):1309-15. doi: 10.1016/s0149-2918(08)80055-0.
5
A comprehensive review of the safety profile of bone morphogenetic protein in spine surgery.骨形态发生蛋白在脊柱手术中安全性概况的全面综述。
Neurosurgery. 2008 May;62(5 Suppl 2):ONS423-31; discussion ONS431. doi: 10.1227/01.neu.0000326030.24220.d8.
6
Stem cells from human fat as cellular delivery vehicles in an athymic rat posterolateral spine fusion model.在无胸腺大鼠后外侧脊柱融合模型中,将人脂肪干细胞作为细胞递送载体。
J Bone Joint Surg Am. 2008 May;90(5):1043-52. doi: 10.2106/JBJS.G.00292.
7
Comparison of human mesenchymal stem cells derived from adipose tissue and bone marrow for ex vivo gene therapy in rat spinal fusion model.大鼠脊柱融合模型中用于体外基因治疗的脂肪组织和骨髓来源的人间充质干细胞的比较
Spine (Phila Pa 1976). 2008 Apr 15;33(8):863-9. doi: 10.1097/BRS.0b013e31816b45c3.
8
Neurologic impairment from ectopic bone in the lumbar canal: a potential complication of off-label PLIF/TLIF use of bone morphogenetic protein-2 (BMP-2).腰椎管内异位骨导致的神经功能损害:骨形态发生蛋白-2(BMP-2)在非标签PLIF/TLIF手术中使用的潜在并发症。
Spine J. 2008 Nov-Dec;8(6):1011-8. doi: 10.1016/j.spinee.2007.06.014. Epub 2007 Nov 26.
9
Beta-TCP bone graft substitutes in a bilateral rabbit tibial defect model.双侧兔胫骨缺损模型中的β-磷酸三钙骨移植替代物
Biomaterials. 2008 Jan;29(3):266-71. doi: 10.1016/j.biomaterials.2007.09.035.
10
A study of the role of nell-1 gene modified goat bone marrow stromal cells in promoting new bone formation.Nell-1基因修饰的山羊骨髓基质细胞在促进新骨形成中作用的研究
Mol Ther. 2007 Oct;15(10):1872-80. doi: 10.1038/sj.mt.6300270. Epub 2007 Jul 24.

冻干 Nell-1 在大鼠脊柱融合模型中的递送。

Delivery of lyophilized Nell-1 in a rat spinal fusion model.

机构信息

Dental and Craniofacial Research Institute, University of California , Los Angeles, Los Angeles, California, USA.

出版信息

Tissue Eng Part A. 2010 Sep;16(9):2861-70. doi: 10.1089/ten.tea.2009.0550.

DOI:10.1089/ten.tea.2009.0550
PMID:20528102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2928135/
Abstract

Nell-1 (Nel-like molecule-1; Nel: protein strongly expressed in neural tissue containing epidermal growth factor-like domain) is a promising osteoblast-specific growth factor for osteoinductive therapies that may circumvent adverse effects, such as nonspecific function and ectopic bone formation, associated with more established osteogenic growth factors such as bone morphogenetic proteins. Beta-tricalcium phosphate (beta-TCP), an osteoconductive, biodegradable ceramic biomaterial, has been used successfully to deliver osteoinducers for bone regeneration. The aim of this study was to develop a carrier system for efficiently delivering biologically active Nell-1 protein. After a 40% initial burst release, beta-TCP particles retained the majority of adsorbed Nell-1 protein in vitro. To test this system in vivo, L4/L5 spinal fusion was performed in three groups of rats (n = 8 each): (1) 5 microg Nell-1 in beta-TCP/demineralized bone matrix putty (DBX); (2) 2.5 microg Nell-1 in beta-TCP/DBX; (3) beta-TCP/DBX only. Fusion was assessed by radiography, palpation, microcomputed tomography, and histological analysis. After 4 weeks, 75% of Nell-1-treated animals exhibited fusion, with a significant increase in new bone volume, whereas only 25% of Nell-free control animals exhibited fusion. Our findings suggest that beta-TCP/DBX can increase both the biochemical stability and biological efficiency of Nell-1 protein.

摘要

Nell-1(神经组织中富含表皮生长因子样结构域的类似分子-1;Nel:蛋白)是一种很有前途的成骨细胞特异性生长因子,可用于骨诱导治疗,以避免与更成熟的成骨生长因子(如骨形态发生蛋白)相关的不良反应,如非特异性功能和异位骨形成。β-磷酸三钙(β-TCP)是一种具有骨传导性和可生物降解的陶瓷生物材料,已成功用于递送骨再生的成骨诱导剂。本研究的目的是开发一种载体系统,以有效递呈具有生物活性的 Nell-1 蛋白。β-TCP 颗粒在体外经过 40%的初始突释后,保留了大部分吸附的 Nell-1 蛋白。为了在体内测试该系统,在三组大鼠(每组 8 只)的 L4/L5 脊柱融合模型中进行了实验:(1)β-TCP/脱矿骨基质糊剂(DBX)中的 5μg Nell-1;(2)β-TCP/DBX 中的 2.5μg Nell-1;(3)仅用β-TCP/DBX。通过 X 线、触诊、微计算机断层扫描和组织学分析评估融合情况。4 周后,75%接受 Nell-1 治疗的动物出现融合,新骨体积显著增加,而Nell-1 缺失的对照组动物中仅有 25%出现融合。我们的研究结果表明,β-TCP/DBX 可以提高 Nell-1 蛋白的生化稳定性和生物学效率。