Zhou Jiarui, Vijayavenkataraman Sanjairaj
The Vijay Lab, Division of Engineering, New York University Abu Dhabi, Abu Dhabi 129188, United Arab Emirates.
Department of Mechanical and Aerospace Engineering, Tandon School of Engineering, New York University, Brooklyn, NY 11201, USA.
Pharmaceutics. 2022 Jan 19;14(2):230. doi: 10.3390/pharmaceutics14020230.
Nerve guidance conduits (NGCs) are tubular scaffolds that act as a bridge between the proximal and distal ends of the native nerve to facilitate the nerve regeneration. The application of NGCs is mostly limited to nerve defects less than 3 mm due to the lack of sufficient cells in the lumen. The development of drug-release-system-embedded NGCs has the potential to improve the nerve regeneration performance by providing long-term release of growth factors. However, most of the past works only focused on one type of drug release system, limiting the variation in drug release system types and features. Therefore, in this study, computer-aided design (CAD) models were constructed and Computational Fluid Dynamics (CFD) simulations were carried out to investigate the effect of growth factor transporting efficiency on different drug release systems. To overcome the challenges posed by the current NGCs in treating long nerve gap injuries (>4 cm), a novel 'relay' NGC design is first proposed in this paper and has the potential to improve the nerve regeneration performance to next level. The intermediate cavities introduced along the length of the multi-channel NGCs act as a relay to further enhance the cell concentrations or growth factor delivery as well as the regeneration performance. Four different drug release systems, namely, a single-layer microsphere system, a double-layer microsphere system, bulk hydrogel, and hydrogel film, were chosen for the simulation. The results show that the double-layer microsphere system achieves the highest growth factor volume fraction among all the drug release systems. For the single-layer microsphere system, growth factor concentration can be significantly improved by increasing the microsphere quantities and decreasing the diameter and adjacent distance of microspheres. Bulk hydrogel systems hold the lowest growth factor release performance, and the growth factor concentration monotonically increased with the increase of film thickness in the hydrogel film system. Owing to the easy fabrication of hydrogel film and the even distribution of growth factors, the hydrogel film system can be regarded as a strong candidate in drug-eluting NGCs. The use of computational simulations can be regarded as a guideline for the design and application of drug release systems, as well as a promising tool for further nerve tissue engineering study.
神经引导导管(NGCs)是一种管状支架,可作为天然神经近端和远端之间的桥梁,以促进神经再生。由于管腔内缺乏足够的细胞,NGCs的应用大多局限于小于3毫米的神经缺损。嵌入药物释放系统的NGCs的开发有可能通过长期释放生长因子来改善神经再生性能。然而,过去的大多数研究仅关注一种类型的药物释放系统,限制了药物释放系统类型和特性的变化。因此,在本研究中,构建了计算机辅助设计(CAD)模型并进行了计算流体动力学(CFD)模拟,以研究生长因子传输效率对不同药物释放系统的影响。为了克服当前NGCs在治疗长神经间隙损伤(>4厘米)时所面临的挑战,本文首次提出了一种新型的“中继”NGCs设计,它有可能将神经再生性能提升到一个新的水平。沿多通道NGCs长度引入的中间腔作为中继,进一步提高细胞浓度或生长因子递送以及再生性能。选择了四种不同的药物释放系统进行模拟,即单层微球系统、双层微球系统、块状水凝胶和水凝胶膜。结果表明,双层微球系统在所有药物释放系统中实现了最高的生长因子体积分数。对于单层微球系统,通过增加微球数量、减小微球直径和相邻距离,可以显著提高生长因子浓度。块状水凝胶系统的生长因子释放性能最低,而在水凝胶膜系统中,生长因子浓度随着膜厚度的增加而单调增加。由于水凝胶膜易于制备且生长因子分布均匀,水凝胶膜系统可被视为药物洗脱NGCs的有力候选者。计算模拟的使用可被视为药物释放系统设计和应用的指南,以及进一步神经组织工程研究的有前途的工具。