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薄膜多电极软质袖带用于选择性神经调节。

Thin Film Multi-Electrode Softening Cuffs for Selective Neuromodulation.

机构信息

Department of Bioengineering, University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX, 75080, USA.

Department of Material Science and Engineering, University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX, 75080, USA.

出版信息

Sci Rep. 2018 Nov 6;8(1):16390. doi: 10.1038/s41598-018-34566-6.

DOI:10.1038/s41598-018-34566-6
PMID:30401906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6219541/
Abstract

Silicone nerve cuff electrodes are commonly implanted on relatively large and accessible somatic nerves as peripheral neural interfaces. While these cuff electrodes are soft (1-50 MPa), their self-closing mechanism requires of thick walls (200-600 µm), which in turn contribute to fibrotic tissue growth around and inside the device, compromising the neural interface. We report the use of thiol-ene/acrylate shape memory polymer (SMP) for the fabrication of thin film multi-electrode softening cuffs (MSC). We fabricated multi-size MSC with eight titanium nitride (TiN) electrodes ranging from 1.35 to 13.95 × 10 cm (1-3 kΩ) and eight smaller gold (Au) electrodes (3.3 × 10 cm; 750 kΩ), that soften at physiological conditions to a modulus of 550 MPa. While the SMP material is not as soft as silicone, the flexural forces of the SMP cuff are about 70-700 times lower in the MSC devices due to the 30 μm thick film compared to the 600 μm thick walls of the silicone cuffs. We demonstrated the efficacy of the MSC to record neural signals from rat sciatic and pelvic nerves (1000 µm and 200 µm diameter, respectively), and the selective fascicular stimulation by current steering. When implanted side-by-side and histologically compared 30 days thereafter, the MSC devices showed significantly less inflammation, indicated by a 70-80% reduction in ED1 positive macrophages, and 54-56% less fibrotic vimentin immunoreactivity. Together, the data supports the use of MSC as compliant and adaptable technology for the interfacing of somatic and autonomic peripheral nerves.

摘要

硅酮神经袖套电极通常被植入相对较大且易于接近的躯体神经作为周围神经接口。虽然这些袖套电极柔软(1-50MPa),但其自闭合机制需要厚壁(200-600μm),这反过来又导致纤维组织在设备周围和内部生长,从而影响神经接口。我们报告了使用硫醇-烯/丙烯酸酯形状记忆聚合物(SMP)来制造薄膜多电极软化袖套(MSC)。我们制造了多尺寸的 MSC,带有 8 个氮化钛(TiN)电极,尺寸范围从 1.35 到 13.95×10cm(1-3kΩ)和 8 个较小的金(Au)电极(3.3×10cm;750kΩ),在生理条件下软化到 550MPa 的模量。虽然 SMP 材料不如硅酮柔软,但由于 SMP 袖套的薄膜厚度为 30μm,而硅酮袖套的壁厚为 600μm,因此 MSC 装置中的弯曲力大约低 70-700 倍。我们证明了 MSC 从大鼠坐骨神经和盆神经(直径分别为 1000μm 和 200μm)记录神经信号的有效性,以及通过电流转向进行选择性束刺激。当并排植入并在 30 天后进行组织学比较时,MSC 装置显示出炎症明显减少,ED1 阳性巨噬细胞减少 70-80%,纤维连接蛋白免疫反应性减少 54-56%。总的来说,这些数据支持 MSC 作为一种顺应性和适应性技术,用于躯体和自主周围神经的接口。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/6629f4e12e0d/41598_2018_34566_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/4a549e646c4d/41598_2018_34566_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/551aa3cbb882/41598_2018_34566_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/a62e24d0200f/41598_2018_34566_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/c33350d84126/41598_2018_34566_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/4d733d078ba2/41598_2018_34566_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/e324b85b8877/41598_2018_34566_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/c99276592c42/41598_2018_34566_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/6629f4e12e0d/41598_2018_34566_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/4a549e646c4d/41598_2018_34566_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/551aa3cbb882/41598_2018_34566_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/a62e24d0200f/41598_2018_34566_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/c33350d84126/41598_2018_34566_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/4d733d078ba2/41598_2018_34566_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/e324b85b8877/41598_2018_34566_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/c99276592c42/41598_2018_34566_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8b/6219541/6629f4e12e0d/41598_2018_34566_Fig8_HTML.jpg

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