Johnson Christopher D L, D'Amato Anthony R, Gilbert Ryan J
Cells Tissues Organs. 2016;202(1-2):116-135. doi: 10.1159/000446621. Epub 2016 Oct 5.
There is currently no cure for individuals with spinal cord injury (SCI). While many promising approaches are being tested in clinical trials, the complexity of SCI limits several of these approaches from aiding complete functional recovery. Several different categories of biomaterials are investigated for their ability to guide axonal regeneration, to deliver proteins or small molecules locally, or to improve the viability of transplanted stem cells. The purpose of this study is to provide a brief overview of SCI, present the different categories of biomaterial scaffolds that direct and guide axonal regeneration, and then focus specifically on electrospun fiber guidance scaffolds. Much like other polymer guidance approaches, electrospun fibers can retain and deliver therapeutic drugs. The experimental section presents new data showing the incorporation of two therapeutic drugs into electrospun poly-L-lactic acid fibers. Two different concentrations of either riluzole or neurotrophin-3 were loaded into the electrospun fibers to examine the effect of drug concentration on the physical characteristics of the fibers (fiber alignment and fiber diameter). Overall, the drugs were successfully incorporated into the fibers and the release was related to the loading concentration. The fiber diameter decreased with the inclusion of the drug, and the decreased diameter was correlated with a decrease in fiber alignment. Subsequently, the study includes considerations for successful incorporation of a therapeutic drug without changing the physical properties of the fibers.
目前,脊髓损伤(SCI)患者尚无治愈方法。虽然许多有前景的方法正在临床试验中进行测试,但SCI的复杂性限制了其中一些方法实现完全功能恢复。人们研究了几种不同类型的生物材料,以了解它们在引导轴突再生、局部递送蛋白质或小分子,或提高移植干细胞活力方面的能力。本研究的目的是简要概述SCI,介绍指导和引导轴突再生的不同类型生物材料支架,然后特别关注电纺纤维引导支架。与其他聚合物引导方法非常相似,电纺纤维可以保留和递送治疗药物。实验部分展示了将两种治疗药物掺入电纺聚-L-乳酸纤维的新数据。将两种不同浓度的利鲁唑或神经营养因子-3加载到电纺纤维中,以研究药物浓度对纤维物理特性(纤维排列和纤维直径)的影响。总体而言,药物成功掺入纤维中,且释放与加载浓度相关。随着药物的加入,纤维直径减小,直径减小与纤维排列的减少相关。随后,该研究包括在不改变纤维物理性质的情况下成功掺入治疗药物的考虑因素。