Shell-core structured nanofibers mediate staged anti-inflammatory and pro-neurogenic activities to repair peripheral nerve

IF 1.8 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Materials Research Express Pub Date : 2024-08-20 DOI:10.1088/2053-1591/ad6afd
Zhichuan Lin, Rui Zhong, Yong Xu, Yan Wu, Chen Ru
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Abstract

The inflammatory reaction significantly impedes the neurogenic process during the restoration of peripheral nerve injury (PNI). Therefore, establishing a non-inflammatory environment is crucial for effective nerve regeneration. This study proposes the use of shell-core structured nanofibers with sequential anti-inflammatory and pro-neurogenic activities to repair PNI. Icariin (ICA), known for its anti-inflammatory effects, was blended with poly(lactic-co-glycolic acid) (PLGA) to form the shell layer’s spinning solution. Concurrently, glial cell-derived neurotrophic factor (GDNF) was combined with graphene oxide (GO) to create the core layer’s spinning solution. These solutions were then subjected to co-axial electrospinning, resulting in shell-core structured GDNF@GO-ICA@PLGA nanofibers. Additionally, a control group of unordered GDNF/GO/ICA/PLGA nanofibers was prepared using conventional electrospinning. The resulting GDNF@GO-ICA@PLGA nanofibers exhibited distinct fibrous structures with a clear shell-core architecture and demonstrated mechanical properties similar to the control group. Notably, the shell-core structured GDNF@GO-ICA@PLGA nanofibers displayed unique staged release kinetics: over 90% ICA was released priorly within the first 0 to 13 days, followed by GDNF release from days 9 to 31. Furthermore, the GDNF@GO-ICA@PLGA nanofibers showed excellent biocompatibility with Schwann cells. In vitro results highlighted the potent anti-inflammatory capabilities of ICA released from the shell layer, while GDNF released from the core layer effectively induced neurogenic differentiation of Schwann cells. The GDNF@GO-ICA@PLGA nanofibers were then processed into a nerve conduit and applied to a 10 mm rat sciatic PNI model. The staged release of ICA and GDNF facilitated by the GDNF@GO-ICA@PLGA nanofibers created a non-inflammatory environment before initiating nerve regeneration, leading to improved PNI restoration. This study underscores the importance of shell-core structured nanofibers in sequentially mediating anti-inflammation and neurogenesis, offering a novel approach for addressing PNI.
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壳核结构纳米纤维介导阶段性抗炎和促神经源活性,修复外周神经
在周围神经损伤(PNI)的恢复过程中,炎症反应会严重阻碍神经源过程。因此,建立非炎症环境对于有效的神经再生至关重要。本研究提出使用具有抗炎和促进神经源活性的壳核结构纳米纤维来修复 PNI。伊卡瑞因(ICA)以其抗炎作用而闻名,它与聚(乳酸-共聚-乙醇酸)(PLGA)混合形成外壳层的纺丝溶液。同时,胶质细胞源性神经营养因子(GDNF)与氧化石墨烯(GO)混合,形成核心层的纺丝溶液。然后对这些溶液进行共轴电纺丝,最终得到壳核结构的 GDNF@GO-ICA@PLGA 纳米纤维。此外,还使用传统电纺丝法制备了一组无序的 GDNF/GO/ICA/PLGA 纳米纤维对照组。所制备的 GDNF@GO-ICA@PLGA 纳米纤维表现出明显的纤维结构,具有清晰的壳核结构,其机械性能与对照组相似。值得注意的是,壳核结构的 GDNF@GO-ICA@PLGA 纳米纤维显示出独特的分阶段释放动力学:90% 以上的 ICA 在最初的 0 至 13 天内释放,随后 GDNF 在第 9 至 31 天释放。此外,GDNF@GO-ICA@PLGA 纳米纤维与许旺细胞具有良好的生物相容性。体外实验结果表明,从外壳层释放的ICA具有强大的抗炎能力,而从芯层释放的GDNF则能有效诱导许旺细胞的神经源分化。然后将 GDNF@GO-ICA@PLGA 纳米纤维加工成神经导管,并应用于 10 毫米大鼠坐骨神经损伤模型。GDNF@GO-ICA@PLGA纳米纤维促进了ICA和GDNF的分阶段释放,在启动神经再生之前创造了一个非炎症性环境,从而改善了PNI的恢复。这项研究强调了壳核结构纳米纤维在依次介导抗炎和神经再生方面的重要性,为解决 PNI 问题提供了一种新方法。
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来源期刊
Materials Research Express
Materials Research Express MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
4.50
自引率
4.30%
发文量
640
审稿时长
12 weeks
期刊介绍: A broad, rapid peer-review journal publishing new experimental and theoretical research on the design, fabrication, properties and applications of all classes of materials.
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