A self-stiffening compliant intracortical microprobe

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Naser Sharafkhani, John M. Long, Scott D. Adams, Abbas Z. Kouzani
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Abstract

Utilising a flexible intracortical microprobe to record/stimulate neurons minimises the incompatibility between the implanted microprobe and the brain, reducing tissue damage due to the brain micromotion. Applying bio-dissolvable coating materials temporarily makes a flexible microprobe stiff to tolerate the penetration force during insertion. However, the inability to adjust the dissolving time after the microprobe contact with the cerebrospinal fluid may lead to inaccuracy in the microprobe positioning. Furthermore, since the dissolving process is irreversible, any subsequent positioning error cannot be corrected by re-stiffening the microprobe. The purpose of this study is to propose an intracortical microprobe that incorporates two compressible structures to make the microprobe both adaptive to the brain during operation and stiff during insertion. Applying a compressive force by an inserter compresses the two compressible structures completely, resulting in increasing the equivalent elastic modulus. Thus, instant switching between stiff and soft modes can be accomplished as many times as necessary to ensure high-accuracy positioning while causing minimal tissue damage. The equivalent elastic modulus of the microprobe during operation is ≈ 23 kPa, which is ≈ 42% less than the existing counterpart, resulting in ≈ 46% less maximum strain generated on the surrounding tissue under brain longitudinal motion. The self-stiffening microprobe and surrounding neural tissue are simulated during insertion and operation to confirm the efficiency of the design. Two-photon polymerisation technology is utilised to 3D print the proposed microprobe, which is experimentally validated and inserted into a lamb’s brain without buckling.

Abstract Image

自刚性顺应性皮质内微探针。
利用柔性皮质内微探针记录/刺激神经元,可最大限度地减少植入微探针与大脑之间的不相容性,从而减少因大脑微动造成的组织损伤。使用生物可溶解涂层材料可暂时使柔性微探针变得坚硬,以承受插入时的穿透力。然而,微探针接触脑脊液后无法调整溶解时间,可能导致微探针定位不准确。此外,由于溶解过程是不可逆的,任何后续的定位误差都无法通过重新加固微探针来纠正。本研究的目的是提出一种皮质内微探针,其中包含两个可压缩结构,使微探针在操作过程中既能适应大脑,又能在插入过程中保持坚硬。插入器施加的压缩力会完全压缩这两个可压缩结构,从而增加等效弹性模量。因此,硬模和软模之间的即时切换可以根据需要多次完成,以确保高精度定位,同时将组织损伤降到最低。工作时微探针的等效弹性模量≈ 23 kPa,比现有的同类产品低≈ 42%,从而使大脑纵向运动时对周围组织产生的最大应变降低≈ 46%。在插入和操作过程中,对自刚性微探针和周围神经组织进行了模拟,以确认设计的效率。利用双光子聚合技术三维打印出了拟议的微探针,经过实验验证,该探针插入羔羊大脑时不会发生弯曲。
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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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