电流体动力制备具有抗菌和增强成骨能力的三层聚己内酯硬脑膜替代物

Yanwen Su , Zhi Li , Hui Zhu , Jiankang He , Boyuan Wei , Dichen Li
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引用次数: 3

摘要

在硬脑膜修复领域,采用模拟天然硬脑膜多层微结构和多种功能的人工替代物来进行有效的神经外科手术至关重要。然而,现有的人工硬脑膜替代品由于结构和力学性能不匹配,以及缺乏抗菌活性或成骨能力,通常会导致并发症。在这项研究中,采用电流体动力(EHD)喷射技术,包括静电纺丝和熔体基EHD打印工艺,制备了三层硬脑膜替代品。采用静电纺丝法制备了高度排列的聚己内酯(PCL)纳米纤维,其内层可模拟天然硬脑膜上排列的胶原纤维。然后通过静电纺丝沉积随机PCL-GS纳米纤维形成中间层。它们的目的是提高制造支架的机械性能。采用熔融EHD法制备不同角度掺杂纳米羟基磷灰石(nHA)的PCL微纤维外层,增强了硬脑膜替代物的成骨能力,促进了硬脑膜替代物与颅骨的融合。三层载药仿生硬脑膜替代物的抗拉强度为22.42±0.89 MPa,断裂伸长率为36.43%±2.00%。GS的加入使其具有抗感染的特性,但不影响其细胞相容性。此外,nHA的掺入促进了三层支架上MC3T3-E1细胞的成骨分化。本研究为多层硬脑膜替代物的制备提供了一种具有抗菌和增强成骨能力性能的有希望的策略,可能为硬脑膜组织修复提供一种新的候选材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrohydrodynamic Fabrication of Triple-layered Polycaprolactone Dura Mater Substitute with Antibacterial and Enhanced Osteogenic Capability

In the field of dura mater repair, it is essential to employ artificial substitutes mimicking the multilayered microarchitecture and multiple functions of native dura mater for effective neurosurgery. However, existing artificial dura mater substitutes commonly cause complications because of mismatched structural and mechanical properties as well as the lack of antibacterial activity or osteogenic capability. In this study, a triple-layered dura mater substitute was fabricated by electrohydrodynamic (EHD) jetting techniques, including electrospinning and melt-based EHD printing processes. Highly aligned polycaprolactone (PCL) nanofibers loaded with gentamicin sulfate (GS) were prepared by electrospinning to form the inner layer, which can mimic the aligned collagen fibers of the native dura mater. Random PCL-GS nanofibers were then deposited by electrospinning to form the middle layer. They were intended to enhance the mechanical properties of the fabricated scaffolds. The outer layer involving PCL microfibers doped with nano-hydroxyapatite (nHA) at various angles was printed by the melting-based EHD method, which can enhance osteogenic capability and promote the fusion between the dura mater substitute and the skull. The tensile strength of the triple-layered drug-loaded biomimetic dura mater substitute was 22.42 ± 0.89 MPa, and the elongation at break was 36.43% ± 2.00%. The addition of GS endowed the substitutes with an anti-infection property without influencing their cytocompatibility. Furthermore, the incorporation of nHA promoted the osteogenic differentiation of MC3T3-E1 cells seeded on the triple-layered scaffolds. This work offers a promising strategy to manufacture multilayered dura mater substitutes with the desired antibacterial and enhanced osteogenic capability performance, possibly providing a novel candidate for dural tissue repair.

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