Department of Mechanical Engineering, University of Utah, Salt Lake City, UT 84112, United States of America.
J Neural Eng. 2017 Dec;14(6):066011. doi: 10.1088/1741-2552/aa867d.
This paper describes the design of a novel drug delivery apparatus integrated with a poly lactic-co-glycolic acid (PLGA) based nerve guide conduit for controlled local delivery of nerve growth factor (NGF) and application in peripheral nerve gap injury.
An NGF dosage curve was acquired to determine the minimum in vitro concentration for optimal neurite outgrowth of dorsal root ganglion (DRG) cells; PLGA based drug delivery devices were then designed and tested in vitro and in vivo across 15 mm rat sciatic nerve gap injury model.
The drug delivery nerve guide was able to release NGF for 28 d at concentrations (0.1-10 ng ml) that were shown to enhance DRG neurite growth. Furthermore, the released NGF was bioactive and able to enhance DRG neurite growth. Following these tests, optimized NGF-releasing nerve conduits were implanted across 15 mm sciatic nerve gaps in a rat model, where they demonstrated significant myelination and muscle innervation in vivo as compared to empty nerve conduits (p < 0.05). This drug delivery nerve guide can release NGF for extended periods of time and enhance axon growth in vitro and in vivo and has the potential to improve nerve regeneration following a peripheral nerve injury.
This integrated drug delivering nerve guide simplifies the design process and provides increased versatility for releasing a variety of different growth factors. This innovative device has the potential for broad applicability and allows for easier customization to change the type of drugs and dosage of individual drugs without devising a completely new biomaterial-drug conjugate each time.
本文描述了一种新型给药装置的设计,该装置与聚乳酸-共-羟基乙酸(PLGA)基神经导管集成在一起,用于控制神经生长因子(NGF)的局部给药,并应用于周围神经间隙损伤。
获得 NGF 剂量曲线,以确定体外最佳背根神经节(DRG)细胞突起生长的最小浓度;然后设计并测试了基于 PLGA 的药物输送装置,在 15mm 大鼠坐骨神经间隙损伤模型中进行了体外和体内测试。
药物输送神经导管能够以浓度(0.1-10ng/ml)释放 NGF 28 天,该浓度被证明能够增强 DRG 轴突生长。此外,释放的 NGF 具有生物活性,能够增强 DRG 轴突生长。经过这些测试,优化的 NGF 释放神经导管被植入大鼠 15mm 坐骨神经间隙,与空神经导管相比,体内显示出明显的髓鞘形成和肌肉神经支配(p<0.05)。这种药物输送神经导管可以长时间释放 NGF,增强体外和体内轴突生长,并有潜力改善周围神经损伤后的神经再生。
这种集成的药物输送神经导管简化了设计过程,为释放各种不同的生长因子提供了更高的通用性。这种创新装置具有广泛的适用性,并允许更容易地定制改变药物的类型和每种药物的剂量,而无需每次都设计全新的生物材料-药物缀合物。