Fully flexible implantable neural probes for electrophysiology recording and controlled neurochemical modulation

被引:4
|
作者
Malekoshoaraie, Mohammad Hassan [1 ]
Wu, Bingchen [2 ,3 ,4 ,5 ]
Krahe, Daniela D. [2 ]
Ahmed, Zabir [1 ]
Pupa, Stephen [1 ]
Jain, Vishal [1 ]
Cui, Xinyan Tracy [2 ,3 ,4 ,5 ]
Chamanzar, Maysamreza [1 ,6 ]
机构
[1] Carnegie Mellon Univ, Elect & Comp Engn, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Bioengn, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Ctr Neural Basis Cognit, Pittburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Pittburgh, PA 15213 USA
[5] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
[6] Carnegie Mellon Univ, Carnegie Mellon Neurosci Inst, Pittsburgh, PA 15213 USA
来源
MICROSYSTEMS & NANOENGINEERING | 2024年 / 10卷 / 01期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
CONVECTION-ENHANCED DELIVERY; CONTROLLED-RELEASE; DRUG-DELIVERY; NEURONS; MICROELECTRODES; ASTROCYTES; DEXAMETHASONE; POLYPYRROLE; RESPONSES; SYSTEM;
D O I
10.1038/s41378-024-00685-6
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Targeted delivery of neurochemicals and biomolecules for neuromodulation of brain activity is a powerful technique that, in addition to electrical recording and stimulation, enables a more thorough investigation of neural circuit dynamics. We have designed a novel, flexible, implantable neural probe capable of controlled, localized chemical stimulation and electrophysiology recording. The neural probe was implemented using planar micromachining processes on Parylene C, a mechanically flexible, biocompatible substrate. The probe shank features two large microelectrodes (chemical sites) for drug loading and sixteen small microelectrodes for electrophysiology recording to monitor neuronal response to drug release. To reduce the impedance while keeping the size of the microelectrodes small, poly(3,4-ethylenedioxythiophene) (PEDOT) was electrochemically coated on recording microelectrodes. In addition, PEDOT doped with mesoporous sulfonated silica nanoparticles (SNPs) was used on chemical sites to achieve controlled, electrically-actuated drug loading and releasing. Different neurotransmitters, including glutamate (Glu) and gamma-aminobutyric acid (GABA), were incorporated into the SNPs and electrically triggered to release repeatedly. An in vitro experiment was conducted to quantify the stimulated release profile by applying a sinusoidal voltage (0.5 V, 2 Hz). The flexible neural probe was implanted in the barrel cortex of the wild-type Sprague Dawley rats. As expected, due to their excitatory and inhibitory effects, Glu and GABA release caused a significant increase and decrease in neural activity, respectively, which was recorded by the recording microelectrodes. This novel flexible neural probe technology, combining on-demand chemical release and high-resolution electrophysiology recording, is an important addition to the neuroscience toolset used to dissect neural circuitry and investigate neural network connectivity.
引用
收藏
页数:17
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