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聚(ε-癸内酯)/银纳米线复合材料作为导电神经接口生物材料的分析

Analysis of a poly(ε-decalactone)/silver nanowire composite as an electrically conducting neural interface biomaterial.

作者信息

Krukiewicz Katarzyna, Fernandez Jorge, Skorupa Małgorzata, Więcławska Daria, Poudel Anup, Sarasua Jose-Ramon, Quinlan Leo R, Biggs Manus J P

机构信息

Centre for Research in Medical Devices (CURAM), Galway Biosciences Research Building, 118 Corrib Village, Newcastle, Galway, Ireland.

Department of Physical Chemistry and Technology of Polymers, Silesian University of Technology, M.Strzody 9, 44-100 Gliwice, Poland.

出版信息

BMC Biomed Eng. 2019 Apr 15;1:9. doi: 10.1186/s42490-019-0010-3. eCollection 2019.

DOI:10.1186/s42490-019-0010-3
PMID:32903306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7422568/
Abstract

BACKGROUND

Advancement in polymer technologies, facilitated predominantly through chemical engineering approaches or through the identification and utilization of novel renewable resources, has been a steady focus of biomaterials research for the past 50 years. Aliphatic polyesters have been exploited in numerous biomedical applications including the formulation of soft-tissue sutures, bone fixation devices, cardiovascular stents etc. Biomimetic 'soft' polymer formulations are of interest in the design of biological interfaces and specifically, in the development of implantable neuroelectrode systems intended to interface with neural tissues. Critically, soft polymer formulations have been shown to address the challenges associated with the disregulation of mechanotransductive processes and micro-motion induced inflammation at the electrode/tissue interface. In this study, a polyester-based poly(ε-decalactone)/silver nanowire (EDL:Ag) composite was investigated as a novel electrically active biomaterial with neural applications.Neural interfaces were formulated through spin coating of a polymer/nanowire formulation onto the surface of a Pt electrode to form a biocompatible EDL matrix supported by a percolated network of silver nanowires. As-formed EDL:Ag composites were characterized by means of infrared spectroscopy, scanning electron microscopy and electrochemical methods, with their cytocompatibility assessed using primary cultures of a mixed neural population obtained from the ventral mesencephalon of Sprague-Dawley rat embryos.

RESULTS

Electrochemical characterization of various EDL:Ag composites indicated EDL:Ag 10:1 as the most favourable formulation, exhibiting high charge storage capacity (8.7 ± 1.0 mC/cm), charge injection capacity (84.3 ± 1.4 μC/cm) and low impedance at 1 kHz (194 ± 28 Ω), outperforming both pristine EDL and bare Pt electrodes. The in vitro biological evaluation showed that EDL:Ag supported significant neuron viability in culture and to promote neurite outgrowth, which had the average length of 2300 ± 6 μm following 14 days in culture, 60% longer than pristine EDL and 120% longer than bare Pt control substrates.

CONCLUSIONS

EDL:Ag nanocomposites are shown to serve as robust neural interface materials, possessing favourable electrochemical characteristics together with high neural cytocompatibility.

摘要

背景

在过去50年里,主要通过化学工程方法或通过识别和利用新型可再生资源推动的聚合物技术进步,一直是生物材料研究的持续重点。脂肪族聚酯已被用于众多生物医学应用,包括软组织缝合线、骨固定装置、心血管支架等的配方。仿生“软”聚合物配方在生物界面设计中具有重要意义,特别是在开发旨在与神经组织连接的可植入神经电极系统方面。至关重要的是,已证明软聚合物配方能够应对与电极/组织界面处机械转导过程失调和微动诱导炎症相关的挑战。在本研究中,研究了一种基于聚酯的聚(ε-癸内酯)/银纳米线(EDL:Ag)复合材料作为一种具有神经应用的新型电活性生物材料。通过将聚合物/纳米线配方旋涂到铂电极表面来制备神经界面,以形成由银纳米线的渗流网络支撑的生物相容性EDL基质。通过红外光谱、扫描电子显微镜和电化学方法对形成的EDL:Ag复合材料进行表征,并使用从Sprague-Dawley大鼠胚胎腹侧中脑获得的混合神经群体的原代培养物评估其细胞相容性。

结果

各种EDL:Ag复合材料的电化学表征表明,EDL:Ag 10:1是最有利的配方,具有高电荷存储容量(8.7±1.0 mC/cm)、电荷注入容量(84.3±1.4 μC/cm)以及在1 kHz时的低阻抗(194±28Ω),优于原始EDL和裸铂电极。体外生物学评估表明,EDL:Ag在培养中支持显著的神经元活力并促进神经突生长,培养14天后平均长度为2300±6μm,比原始EDL长60%,比裸铂对照底物长120%。

结论

EDL:Ag纳米复合材料被证明是强大的神经界面材料,具有良好的电化学特性以及高神经细胞相容性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/4442f4a383d8/42490_2019_10_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/4442f4a383d8/42490_2019_10_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/67f06fbdef7c/42490_2019_10_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/779109b8c3c2/42490_2019_10_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/49bb8ced4278/42490_2019_10_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a60/7422568/fbbd64b23f97/42490_2019_10_Fig6_HTML.jpg
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