用于神经胶质瘢痕治疗的抗炎聚合物电极:将概念想法带入未来的结果。

Frontiers in neuroengineering Pub Date : 2014-05-13 eCollection Date: 2014-01-01 DOI:10.3389/fneng.2014.00009
Maria Asplund, Christian Boehler, Thomas Stieglitz
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引用次数: 24

摘要

导电聚合物薄膜为植入微电极的功能化提供了一种方便的途径,同时又不影响其作为优异记录单元的性能。一层微米厚的涂层,沉积在一个普通的金属电极表面,可以洗脱用于治疗神经胶质瘢痕的抗炎药物,以及用于支持周围神经元的生长因子。聚合物的电活化驱动物质的释放,理想地提供了一种可靠的方法来控制释放的数量和时间。驱动信号的形式是恒定电位(CP),缓慢氧化还原扫描或快速脉冲都表示在文献中。很少有研究表明实际记录和刺激微电子设备在体内释放这种物质。有必要弥合基于体外释放的研究与预期应用之间的差距,这将意味着释放到活的和高度脆弱的组织中。在生物环境中,信号受到可用电子设备和生物安全性的限制。驾驶信号不能对组织有害,也不能以不受控制的方式激活组织。这篇综述旨在揭示如何选择合适的驱动参数的聚合物电极在体内设置。它汇集了有关神经元激活阈值和损伤阈值的信息,并将其与已知的有效驱动导电聚合物薄膜释放的内容联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results.

Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results.

Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results.

Anti-inflammatory polymer electrodes for glial scar treatment: bringing the conceptual idea to future results.

Conducting polymer films offer a convenient route for the functionalization of implantable microelectrodes without compromising their performance as excellent recording units. A micron thick coating, deposited on the surface of a regular metallic electrode, can elute anti-inflammatory drugs for the treatment of glial scarring as well as growth factors for the support of surrounding neurons. Electro-activation of the polymer drives the release of the substance and should ideally provide a reliable method for controlling quantity and timing of release. Driving signals in the form of a constant potential (CP), a slow redox sweep or a fast pulse are all represented in literature. Few studies present such release in vivo from actual recording and stimulating microelectronic devices. It is essential to bridge the gap between studies based on release in vitro, and the intended application, which would mean release into living and highly delicate tissue. In the biological setting, signals are limited both by available electronics and by the biological safety. Driving signals must not be harmful to tissue and also not activate the tissue in an uncontrolled manner. This review aims at shedding more light on how to select appropriate driving parameters for the polymer electrodes for the in vivo setting. It brings together information regarding activation thresholds for neurons, as well as injury thresholds, and puts this into context with what is known about efficient driving of release from conducting polymer films.

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