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Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment

机译:生物聚合物 - 纳米管神经引导导管用于外周神经再生的药物递送:体内结构和功能评估

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Peripheral nerve injuries account for roughly 3% of all trauma patients with over 900,000 repair procedures annually in the US. Of all extremity peripheral nerve injuries, 51% require nerve repair with a transected gap. The current gold-standard treatment for peripheral nerve injuries, autograft repair, has several shortcomings. Engineered constructs are currently only suitable for short gaps or small diameter nerves. Here, we investigate novel nerve guidance conduits with aligned microchannel porosity that deliver sustained-release of neurogenic 4-aminopyridine (4-AP) for peripheral nerve regeneration in a critical-size (15?mm) rat sciatic nerve transection model. The results of functional walking track analysis, morphometric evaluations of myelin development, and histological assessments of various markers confirmed the equivalency of our drug-conduit with autograft controls. Repaired nerves showed formation of thick myelin, presence of S100 and neurofilament markers, and promising functional recovery. The conduit's aligned microchannel architecture may play a vital role in physically guiding axons for distal target reinnervation, while the sustained release of 4-AP may increase nerve conduction, and in turn synaptic neurotransmitter release and upregulation of critical Schwann cell neurotrophic factors. Overall, our nerve construct design facilitates efficient and efficacious peripheral nerve regeneration via a drug delivery system that is feasible for clinical applications.
机译:周围神经损伤占所有创伤患者的大约3%,在美国每年每年每年都有900,000次修复程序。在所有极端周围神经损伤中,51%需要具有透过间隙的神经修复。目前对周围神经损伤的金标准治疗,自体移植修复,具有几个缺点。工程构建体目前仅适用于短的间隙或小直径神经。在这里,我们研究了一种新的神经引导导管,所述微通道孔隙率与对齐的微通道孔隙率,其在临界大小(15μm)大鼠坐骨神经转向模型中为周围神经再生提供神经源性4-氨基吡啶(4-AP)的持续释放。功能行走轨道分析的结果,髓鞘发育的形态学评价以及各种标志物的组织学评估证实了我们对自体移植管制的药管的等效性。修复的神经显示厚髓鞘的形成,S100和神经膜标记的存在,并且有希望的功能恢复。导管的对齐的微通道架构可能在物理引导轴突中发挥重要作用,用于远端目标重新衰减,而4-AP的持续释放可能会增加神经传导,并且反过来突触神经递质释放和临界施曼细胞神经营养因子的上调。总体而言,我们的神经构建设计通过可用于临床应用的药物递送系统促进有效和有效的周围神经再生。

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