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3D Parylene sheath neural probe for chronic recordings

机译:3D聚对二甲苯鞘神经探针,用于慢性记录

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摘要

Objective. Reliable chronic recordings from implanted neural probes remain a significant challenge; current silicon-based and microwire technologies experience a wide range of biotic and abiotic failure modes contributing to loss of signal quality. Approach. A multi-prong alternative strategy with potential to overcome these hurdles is introduced that combines a novel three dimensional (3D), polymer-based probe structure with coatings. Specifically, the Parylene C sheath-based neural probe is coated with neurotrophic and anti-inflammatory factors loaded onto a Matrigel carrier to encourage the ingrowth of neuronal processes for improved recording quality, reduce the immune response, and promote improved probe integration into brain tissue for reliable, long-term implementation compared to its rigid counterparts. Main results. The 3D sheath structure of the probe was formed by thermal molding of a surface micromachined Parylene C microchannel, with electrode sites lining the interior and exterior regions of the lumen. Electrochemical characterization of the probes via cyclic voltammetry and electrochemical impedance spectroscopy was performed and indicated suitable electrode properties for neural recordings (1 kHz electrical impedance of ~200 kΩ in vitro). A novel introducer tool for the insertion of the compliant polymer probe into neural tissue was developed and validated both in vitro using agarose gel and in vivo in the rat cerebral cortex. In vivo electrical functionality of the Parylene C-based 3D probes and their suitability for recording the neuronal activity over a 28-day period was demonstrated by maintaining the 1 kHz electrical impedance within a functional range (<400 kΩ) and achieving a reasonably high signal-to-noise ratio for detection of resolvable multi-unit neuronal activity on most recording sites in the probe. Immunohistochemical analysis of the implant site indicated strong correlations between the quality of recorded activity and the neuronal/astrocytic density around the probe. Significance. The provided electrophysiological and immunohistochemical data provide strong support to the viability of the developed probe technology. Furthermore, the obtained data provide insights into further optimization of the probe design, including tip geometry, use of neurotrophic and anti-inflammatory drugs in the Matrigel coating, and placement of the recording sites.
机译:目的。从植入的神经探针获得可靠的慢性记录仍然是一个重大挑战。当前的硅基和微线技术经历了多种生物和非生物故障模式,这些信号模式导致信号质量下降。方法。介绍了一种有潜力克服这些障碍的多管脚替代策略,该策略将新颖的三维(3D),基于聚合物的探针结构与涂层相结合。具体而言,基于Parylene C鞘的神经探针在神经胶质载体上涂有神经营养和抗炎因子,以促进神经元过程向内生长,从而改善记录质量,降低免疫反应并促进探针整合到脑组织中,与严格的同类产品相比,该产品可靠,长期的实施。主要结果。探针的3D鞘结构是通过表面微机械加工的Parylene C微通道的热成型而形成的,电极位置排列在管腔的内部和外部区域。通过循环伏安法和电化学阻抗谱对探针进行了电化学表征,并为神经记录指出了合适的电极特性(体外1kHz的电阻抗为200kΩ)。开发了一种用于将顺应性聚合物探针插入神经组织的新型引入工具,并在体外使用琼脂糖凝胶和在大鼠大脑皮层体内进行了验证。通过将1 kHz电阻抗保持在功能范围内(<400kΩ)并获得相当高的信号,证明了基于Parylene C的3D探针的体内电功能及其在28天时间内记录神经元活动的适用性噪声比,用于检测探针中大多数记录位点上可分辨的多单位神经元活性。植入部位的免疫组织化学分析表明,记录的活动质量与探针周围的神经元/星形细胞密度之间存在很强的相关性。意义。提供的电生理和免疫组化数据为已开发的探针技术的可行性提供了有力的支持。此外,获得的数据为进一步优化探针设计提供了见识,包括针尖几何形状,在Matrigel涂层中使用神经营养和抗炎药以及记录部位的位置。

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  • 来源
    《Journal of neural engineering》 |2013年第4期|045002.1-045002.16|共16页
  • 作者单位

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Independent Consultant, Los Angeles, CA 90017, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA;

    Huntington Medical Research Institutes, 734 Fairmount Avenue, Pasadena, CA 91105-3104, USA;

    Department of Biomedical Engineering, University of Southern California, 1042 Downey Way, DRB-140, Los Angeles, CA 90089-1111, USA,Ming Hsieh Department of Electrical Engineering, University of Southern California, 3740 McClintock Ave, EEB-100, Los Angeles, CA 90089-2560, USA;

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