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用于聚对二甲苯鞘神经探针的基质胶涂层

Matrigel coatings for Parylene sheath neural probes.

作者信息

Lee Curtis D, Hara Seth A, Yu Lawrence, Kuo Jonathan T W, Kim Brian J, Hoang Tuan, Pikov Victor, Meng Ellis

机构信息

Department of Biomedical Engineering, University of Southern California, Los Angeles, California, 90089-1111.

Neural Engineering Program, Huntington Medical Research Institutes, Pasadena, California, 91105-3104.

出版信息

J Biomed Mater Res B Appl Biomater. 2016 Feb;104(2):357-68. doi: 10.1002/jbm.b.33390. Epub 2015 Mar 23.

Abstract

The biologically derived hydrogel Matrigel (MG) was used to coat a Parylene-based sheath intracortical electrode to act as a mechanical and biological buffer as well as a matrix for delivering bioactive molecules to modulate the cellular response and improve recording quality. MG was loaded with dexamethasone to reduce the immune response together with nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) to maintain neuronal density and encourage neuronal ingrowth toward electrodes within the sheath. Coating the Parylene sheath electrode with the loaded MG significantly improved the signal-to-noise ratio for neural events recorded from the motor cortex in rat for more than 3 months. Electron microscopy showed even coverage of both the Parylene substrate and the platinum recording electrodes. Electrochemical impedance spectroscopy (EIS) of coated electrodes in 1× phosphate-buffered saline demonstrated low impedance required for recording neural signals. This result was confirmed by in vivo EIS data, showing significantly decreased impedance during the first week of recording. Dexamethasone, NGF, and BDNF loaded into MG were released within 1 day in 1× phosphate-buffered saline. Although previous studies showed that MG loaded with either the immunosuppressant or the neurotrophic factor cocktail provided modest improvement in recording quality in a 1-month in vivo study, the combination of these bioactive molecules did not improve the signal quality over coating probes with only MG in a 3-month in vivo study. The MG coating may further improve recording quality by optimizing the in vivo release profile for the bioactive molecules.

摘要

生物衍生水凝胶基质胶(MG)被用于涂覆聚对二甲苯基鞘内皮层电极,以充当机械和生物缓冲层以及用于递送生物活性分子的基质,从而调节细胞反应并提高记录质量。MG中加载了地塞米松以降低免疫反应,同时加载了神经生长因子(NGF)和脑源性神经营养因子(BDNF)以维持神经元密度并促进神经元向鞘内电极生长。用加载了MG的材料涂覆聚对二甲苯鞘电极显著提高了从大鼠运动皮层记录的神经事件的信噪比,持续超过3个月。电子显微镜显示聚对二甲苯基底和铂记录电极均被均匀覆盖。涂覆电极在1×磷酸盐缓冲盐水中的电化学阻抗谱(EIS)表明记录神经信号所需的阻抗较低。体内EIS数据证实了这一结果,显示在记录的第一周内阻抗显著降低。加载到MG中的地塞米松、NGF和BDNF在1×磷酸盐缓冲盐水中1天内释放。尽管先前的研究表明,在为期1个月的体内研究中,加载免疫抑制剂或神经营养因子混合物的MG在记录质量方面有适度改善,但在为期3个月的体内研究中,这些生物活性分子的组合并没有比仅用MG涂覆探针提高信号质量。MG涂层可能通过优化生物活性分子的体内释放曲线进一步提高记录质量。

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