Active MEMS Neural Clamps
Active MEMS Neural Clamps
批准号:
6868269
负责人:
Ranu Jung
金额:
$18.06万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2007-03-31
关键词:
Ranabioengineering /biomedical engineeringbiomedical equipment developmentbody temperatureclinical biomedical equipmentelectrodeselectrophysiologylaboratory ratlumbar plexusmedical implant scienceminiature biomedical equipmentneuromuscular stimulatorphrenic nervephysical propertysiliconspinal nervesvoltage /patch clamp
中文摘要
描述(由申请人提供):有源MEMS神经夹在过去的十年中,重大的技术和科学进步导致了运动控制神经假体设备的发展。此类设备控制系统进一步发展的一个重要方面是能够长期获得稳定的时空分布神经活动记录。类似地,需要能够提供神经组织的时空分布刺激的神经接口。在这个项目中,我们专注于开发一种新的方法来记录周围神经系统的分布式神经活动,特别是哺乳动物的脊髓根。目标是建模,设计,制造,测试和表征基于微机电系统(MEMS)的神经电极,这些电极主动夹持在脊柱根部上。该夹持机构将提供可逆的安全附接机构,以确保神经信号的可靠记录。夹紧将由植入部位的体温驱动。在植入过程中,通过局部灌注冷却的盐溶液,可以暂时逆转夹持以重新定位。在有限元建模方法的指导下,制造将使用与集成电路制造兼容的硅晶片批处理技术,以便能够在未来开发用于滤波、放大和信号处理的片上电子器件。硅晶片制造还使得未来能够开发低成本器件。通过批量处理,我们可以在单个晶圆上改变电极和器件特性,以优化性能。最初将使用两栖动物神经评价同一器械上的几种电极配置,然后使用固定的啮齿动物神经,最终通过记录大鼠颈脊神经根和膈神经的自主呼吸活动进行实时评价。将评价将电极放置在多个腰骶脊神经根上的能力。这些结果将指导电极的重新设计。该新颖设计允许重新定位多个空间分布的可植入电极的能力。这种电极将提高我们对清醒受试者的神经功能进行科学研究的能力,并开发用于康复的先进神经假体产品。
英文摘要
DESCRIPTION (provided by applicant): ACTIVE MEMS NEURAL CLAMPS In the past decade, significant technological and scientific advances have led to the development of neuroprosthetic devices for motor control. An important aspect in the further advancement of the control systems for such devices will be the ability to obtain stable spatiotemporally distributed recording of neural activity chronically. Similarly, neural interfaces that can provide spatiotemporally distributed stimulation of neural tissue are required. In this project, we are focusing on the development of a novel approach of recording distributed neural activity from the peripheral nervous system, in particular the mammalian spinal roots. The goal is to model, design, fabricate, test and characterize Microelectromechanical System (MEMS) based neural electrodes that actively clamp onto the spinal roots. This clamping mechanism will provide a reversible secure attachment mechanism to ensure reliable recording of the neural signals. The clamping will be driven by the body temperature at site of the implant. The clamping can be temporarily reversed for repositioning during the implant procedure by local perfusion of cooled saline solutions. The fabrication, guided by a finite element modeling approach, will use silicon wafer batch processing techniques that are compatible with integrated circuit manufacturing in order to enable future development of on-chip electronics for filtering, amplification and signal processing. The silicon wafer fabrication also enables future development of low-cost devices. With batch processing, we can vary the electrode and device characteristics on a single wafer to optimize performance. Several electrode configurations on the same device will be evaluated initially using amphibian nerve, then with fixed rodent nerve, and ultimately in real-time by recording autonomous respiratory activity from rat cervical spinal roots and the phrenic nerve. Ability to place the electrodes on multiple lumbosacral spinal roots will be evaluated. These results will guide the redesign of the electrodes. The novel design allows capability for repositioning of multiple spatially distributed implantable electrodes. Such electrodes will advance our capabilities of scientific investigation of neural function in awake subjects and in the development of advanced neuroprosthetic products for rehabilitation.
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会议论文
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