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Injectable biopolymer gel compositions for neural tissue repair.

机译:用于神经组织修复的可注射生物聚合物凝胶组合物。

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摘要

Injuries to the brain, spinal cord or other central nervous system (CNS) tissues trigger a cascade of biochemical events that result in an environment that is unfavorable for axonal regeneration and re-establishment of functional connections. Advances in understanding of the cellular and molecular mechanisms underlying spinal cord injury (SCI) over the past twenty years have resulted in the development of a number of therapeutic approaches to treating this critical problem. Biomaterial constructs represent an important and perhaps essential component of spinal cord repair strategies; however the functional and restorative potential of these approaches has not yet been realized.;This research focused on the development, synthesis and properties of biopolymer gel compositions for neural tissue repair. The primary goal was to prepare injectable gels which could function to bridge the lesion, prevent development or progression of a cystic cavity and provide a favorable terrain for axonal regeneration by delivering cells or other growth-promoting factors to the injured spinal cord. Homogeneous alginate (ALG), alginate-carboxymethylcellulose (ALG-CMC) and alginate-hyaluronic acid (ALG-HA) gels suitable for soft tissue engineering applications were synthesized via ionic crosslinking. Gradual gelation was achieved by slow liberation of calcium ions from calcium carbonate by reaction with D-glucono-delta-lactone (GDL). In situ-forming ALG, ALG-CMC and ALG-HA gels have not previously been studied as biopolymer matrices for SCI repair.;All compositions were injectable through a 22-gauge needle prior to crosslinking. Gelation timing was evaluated as a function of biopolymer composition, calcium content, and temperature, and ranged from one to three hours for the conditions studied. Swelling and stability of gels were evaluated in vitro, and oscillatory tests were used to examine rheological properties. The potential for ALG, ALG-CMC and ALG-HA gels as transplantation matrices was investigated by incorporating Schwann cells in gel compositions in vitro.;A pilot animal study was conducted to demonstrate proof of concept in vivo using a clinically relevant SCI model in adult rats. Study animals received midline cervical contusion injuries at C3/C4 using an Infinite Horizon impactor and were treated with an ALG-CMC gel one week later. Histology revealed that the compositions integrated well with host spinal cord tissue and did not initiate a significant inflammatory response. Treated animals also showed minimal evidence of cystic cavitation. Results suggest that injectable alginate-based compositions have significant potential for minimally-invasive treatment of SCI and should undergo further investigation and optimization for neural tissue repair.
机译:对脑,脊髓或其他中枢神经系统(CNS)组织的伤害会触发一系列的生化事件,从而导致不利于轴突再生和功能连接重建的环境。在过去的20年中,对了解脊髓损伤(SCI)的细胞和分子机制的了解的进步导致了许多治疗该关键问题的治疗方法的发展。生物材料构建体代表了脊髓修复策略的重要甚至必不可少的组成部分。然而,这些方法的功能和修复潜力尚未实现。这项研究的重点是用于神经组织修复的生物聚合物凝胶组合物的开发,合成和性质。主要目标是制备可注射的凝胶,其可通过将细胞或其他促进生长的因子递送至受伤的脊髓而起到弥合病变,防止囊性腔发展或进展并为轴突再生提供有利地形的作用。通过离子交联合成了适用于软组织工程应用的均相海藻酸盐(ALG),海藻酸盐-羧甲基纤维素(ALG-CMC)和海藻酸盐-透明质酸(ALG-HA)凝胶。通过与D-葡萄糖酸-δ-内酯(GDL)反应从碳酸钙中缓慢释放钙离子来实现逐步胶凝。原位形成的ALG以前尚未研究过ALG-CMC和ALG-HA凝胶作为SCI修复的生物聚合物基质。所有组合物在交联之前都可通过22号针头注射。评估胶凝时间是生物聚合物组成,钙含量和温度的函数,在所研究的条件下,胶凝时间为1-3小时。在体外评估凝胶的溶胀和稳定性,并使用振荡测试来检查流变特性。通过在体外将Schwann细胞掺入凝胶组合物中来研究ALG,ALG-CMC和ALG-HA凝胶作为移植基质的潜力。;进行了一项先导动物研究,以使用临床相关SCI模型在成人体内进行概念验证大鼠。研究动物使用Infinite Horizo​​n冲击器在C3 / C4处遭受中线颈椎挫伤,并在一周后接受ALG-CMC凝胶治疗。组织学显示该组合物与宿主脊髓组织很好地整合,并且没有引发明显的炎症反应。经治疗的动物也没有出现囊性空化的迹象。结果表明,基于藻酸盐的可注射组合物具有微创治疗SCI的巨大潜力,应进一步研究和优化神经组织修复。

著录项

  • 作者

    Barnes, Samesha Rosanne.;

  • 作者单位

    University of Florida.;

  • 授予单位 University of Florida.;
  • 学科 Engineering Materials Science.;Engineering Biomedical.;Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 123 p.
  • 总页数 123
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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