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本文引用的文献

1
Annular repair using high-density collagen gel: a rat-tail in vivo model.采用高密度胶原凝胶进行环状修复:大鼠体内模型。
Spine (Phila Pa 1976). 2014 Feb 1;39(3):198-206. doi: 10.1097/BRS.0000000000000103.
2
Mechanical consequences of annular tears and subsequent intervertebral disc degeneration.椎间盘环撕裂及随后椎间盘退变的力学后果。
Clin Biomech (Bristol). 1994 Jul;9(4):211-9. doi: 10.1016/0268-0033(94)90001-9.
3
Challenges and strategies in the repair of ruptured annulus fibrosus.纤维环破裂修复的挑战与策略。
Eur Cell Mater. 2013 Jan 2;25:1-21. doi: 10.22203/ecm.v025a01.
4
Biomechanical performance of rigid compared to dynamic anterior cervical plating: analysis of adjacent upper and lower level compressive forces.与动态前路颈椎板相比,刚性的生物力学性能:分析相邻上下水平的压缩力。
J Clin Neurosci. 2012 Dec;19(12):1706-10. doi: 10.1016/j.jocn.2012.03.026. Epub 2012 Oct 17.
5
Characterization of riboflavin-modified dentin collagen matrix.核黄素修饰牙本质胶原基质的特性研究。
J Dent Res. 2012 Nov;91(11):1049-54. doi: 10.1177/0022034512459053. Epub 2012 Aug 22.
6
Migration of intervertebral disc cells into dense collagen scaffolds intended for functional replacement.椎间盘细胞向用于功能替代的致密胶原支架中的迁移。
J Mater Sci Mater Med. 2012 Mar;23(3):813-21. doi: 10.1007/s10856-011-4545-7. Epub 2012 Jan 5.
7
Penetrating annulus fibrosus injuries affect dynamic compressive behaviors of the intervertebral disc via altered fluid flow: an analytical interpretation.穿透性纤维环损伤通过改变液体流动影响椎间盘的动态压缩行为:一种分析性解释。
J Biomech Eng. 2011 Aug;133(8):084502. doi: 10.1115/1.4004915.
8
Tissue-engineered intervertebral discs produce new matrix, maintain disc height, and restore biomechanical function to the rodent spine.组织工程化的椎间盘可产生新的基质,维持椎间盘高度,并恢复啮齿动物脊柱的生物力学功能。
Proc Natl Acad Sci U S A. 2011 Aug 9;108(32):13106-11. doi: 10.1073/pnas.1107094108. Epub 2011 Aug 1.
9
Genipin-crosslinked fibrin hydrogels as a potential adhesive to augment intervertebral disc annulus repair.基因素交联纤维蛋白水凝胶作为一种潜在的黏合剂,用于增强椎间盘纤维环修复。
Eur Cell Mater. 2011 Apr 18;21:373-83. doi: 10.22203/ecm.v021a28.
10
Construction of tissue-engineered composite intervertebral disc and preliminary morphological and biochemical evaluation.构建组织工程化复合椎间盘中初步的形态学和生物化学评估
Biochem Biophys Res Commun. 2011 Apr 8;407(2):327-32. doi: 10.1016/j.bbrc.2011.03.015. Epub 2011 Mar 5.

用于纤维环修复的可注射高密度胶原蛋白凝胶:大鼠尾部体外模型

Injectable, high-density collagen gels for annulus fibrosus repair: An in vitro rat tail model.

作者信息

Borde Brandon, Grunert Peter, Härtl Roger, Bonassar Lawrence J

机构信息

Department of Biomedical Engineering, Cornell University, Ithaca, New York.

Department of Neurological Surgery, Weill Cornell Medical College, New York, New York.

出版信息

J Biomed Mater Res A. 2015 Aug;103(8):2571-81. doi: 10.1002/jbm.a.35388. Epub 2014 Dec 29.

DOI:10.1002/jbm.a.35388
PMID:25504661
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4465422/
Abstract

A herniated intervertebral disc often causes back pain when disc tissue is displaced through a damaged annulus fibrosus. Currently, the only methods available for annulus fibrosus repair involve mechanical closure of defect, which does little to address biological healing in the damaged tissue. Collagen hydrogels are injectable and have been used to repair annulus defects in vivo. In this study, high-density collagen hydrogels at 5, 10, and 15 mg/mL were used to repair defects made to intact rat caudal intervertebral discs in vitro. A group of gels at 15 mg/mL were also cross-linked with riboflavin at 0.03 mM, 0.07 mM, or 0.10 mM. These cross-linked, high-density collagen gels maintained their presence in the defect under loading and contributed positively to the mechanical response of damaged discs. Discs exhibited increases to 95% of undamaged effective equilibrium and instantaneous moduli as well as up to fourfold decreases in effective hydraulic permeability from the damaged discs. These data suggest that high-density collagen gels may be effective at restoring mechanical function of injured discs as well as potential vehicles for the delivery of biological agents such as cells or growth factors that may aid in the repair of the annulus fibrosus.

摘要

当椎间盘组织通过受损的纤维环移位时,椎间盘突出通常会导致背痛。目前,唯一可用于修复纤维环的方法是机械性闭合缺损,这对受损组织的生物愈合几乎没有作用。胶原蛋白水凝胶可注射,已被用于体内修复纤维环缺损。在本研究中,使用浓度为5、10和15mg/mL的高密度胶原蛋白水凝胶在体外修复完整大鼠尾椎椎间盘制造的缺损。一组浓度为15mg/mL的水凝胶还用0.03mM、0.07mM或0.10mM的核黄素进行交联。这些交联的高密度胶原蛋白凝胶在加载情况下能在缺损处保持存在,并对受损椎间盘的力学反应有积极贡献。椎间盘的有效平衡模量和瞬时模量增加到未受损时的95%,有效水力渗透率比受损椎间盘降低了四倍之多。这些数据表明,高密度胶原蛋白凝胶可能有效地恢复受损椎间盘的力学功能,并且可能是递送生物制剂(如细胞或生长因子)的潜在载体,这些生物制剂可能有助于纤维环的修复。