Centre for Nanotechnology and Advanced Biomaterials, ABCDE Innovation Centre, School of Chemical and Biotechnology, SASTRA Deemed University, Thanjavur 613 401, India.
ACS Appl Bio Mater. 2024 Oct 21;7(10):6706-6719. doi: 10.1021/acsabm.4c00872. Epub 2024 Sep 30.
Reuniting denuded nerve ends after a long segmental peripheral nerve defect is challenging due to delayed axonal regeneration and incomplete, nonspecific reinnervation, as conventional hollow nerve guides fail to ensure proper fascicular complementation and obstruct axonal guidance across the defects. This study focuses on fabricating multifilament conduits using a plant-derived anionic polysaccharide, pectin, where the abundant availability of carboxylate (COO-) functional groups in pectin facilitates instantaneous sol-gel transition upon interaction with divalent cations. Despite their advantages, pectin hydrogels encounter structural instability under physiological conditions. Hence, pectin is conjugated with light-sensitive methacrylate residues (49.8% methacrylation) to overcome these issues, enabling the fabrication of dual cross-linked multifilament nerve conduits through an ionic interaction-driven, template-free 3D wet writing process, followed by photo-cross-linking at 525 nm. The anatomical equivalence including peri-, epi-, and endoneurium structures of the customized multifilament conduits was confirmed through scanning electron micrographs and micro-CT analysis of rat and goat sciatic nerve tissues. Furthermore, the fabricated multifilament nerve conduits demonstrated cytocompatibility and promoted the expression of neuron-specific intermediate filament protein (NF-200) in PC12 cells and neurite outgrowth of 16.90 ± 1.82 μm on day 14. Micro-CT imaging of an anastomosed native goat sciatic nerve with an 8-filament conduit demonstrated precise fascicular complementation in an ex vivo interpositional goat model. This approach not only eliminates the need for a suture-intensive ligation process but also highlights the customizability of multifilament conduits to meet patient- and injury-specific needs.
在长节段周围神经缺损后重新连接裸露的神经末端具有挑战性,这是由于轴突再生延迟和不完全、非特异性的再支配,因为传统的空心神经导管不能确保适当的束状补充,并阻碍轴突穿过缺损的导向。本研究专注于使用植物源性阴离子多糖果胶来制造多丝导管,其中果胶中丰富的羧酸盐 (COO-) 官能团在与二价阳离子相互作用时促进瞬时溶胶-凝胶转变。尽管果胶水凝胶具有优势,但在生理条件下它们会遇到结构不稳定的问题。因此,将果胶与光敏感的甲基丙烯酰基残基(49.8%甲基丙烯酰化)偶联以克服这些问题,通过离子相互作用驱动、无模板的 3D 湿写工艺制造双交联多丝神经导管,然后在 525nm 处进行光交联。通过扫描电子显微镜和大鼠和山羊坐骨神经组织的微 CT 分析,确认了定制多丝导管的解剖等效性,包括周围、神经外膜和神经内膜结构。此外,所制造的多丝神经导管表现出细胞相容性,并在 PC12 细胞中促进神经元特异性中间丝蛋白 (NF-200) 的表达和 14 天 16.90 ± 1.82μm 的神经突生长。吻合的天然山羊坐骨神经与 8 丝导管的微 CT 成像显示,在外置山羊模型中精确地补充了束状结构。这种方法不仅消除了对缝线密集结扎过程的需求,还突出了多丝导管的可定制性,以满足患者和损伤的特定需求。