Surface modification of neural recording electrodes with conducting polymer/biomolecule blends.

The interface between micromachined neural microelectrodes and neural tissue plays an important role in chronic in vivo recording. Electrochemical polymerization was used to optimize the surface of the metal electrode sites. Electrically conductive polymers (polypyrrole) combined with biomolecules having cell adhesion functionality were deposited with great precision onto microelectrode sites of neural probes. The biomolecules used were a silk-like polymer having fibronectin fragments (SLPF) and nonapeptide CDPGYIGSR. The existence of protein polymers and peptides in the coatings was confirmed by reflective microfocusing Fourier transform infrared spectroscopy (FTIR). The morphology of the coating was rough and fuzzy, providing a high density of bioactive sites for interaction with neural cells. This high interfacial area also helped to lower the impedance of the electrode site and, consequently, to improve the signal transport. Impedance spectroscopy showed a lowered magnitude and phase of impedance around the biologically relevant frequency of 1 kHz. Cyclic voltammetry demonstrated the intrinsic redox reaction of the doped polypyrrole and the increased charge capacity of the coated electrodes. Rat glial cells and human neuroblastoma cells were seeded and cultured on neural probes with coated and uncoated electrodes. Glial cells appeared to attach better to polypyrrole/SLPF-coated electrodes than to uncoated gold electrodes. Neuroblastoma cells grew preferentially on and around the polypyrrole/CDPGYIGSR-coated electrode sites while the polypyrrole/CH(3)COO(-)-coated sites on the same probe did not show a preferential attraction to the cells. These results indicate that we can adjust the chemical composition, morphology, electronic transport, and bioactivity of polymer coatings on electrode surfaces on a multichannel micromachined neural probe by controlling electrochemical deposition conditions.

Evoked vertex and inferior colliculus responses to electrical stimulation of the cochlear nucleus.

Evoked potentials were recorded from the vertex and the inferior colliculus in guinea pigs in response to electrical stimulation of the cochlear nucleus complex. The stimuli consisted of 80-microseconds biphasic pulses, ranging from 20 to 5,000 microA. The effect of electrode location (nerve root area, surface, and in-depth dorsal cochlear nucleus) on the evoked response was assessed by measuring amplitudes, latencies, and thresholds as a function of stimulating current levels. Stimulation of the nerve root area resulted in the shortest latencies, the largest amplitudes, and the lowest thresholds, whereas the surface of the dorsal cochlear nucleus was the least effective stimulating site.

Surgical implantation and biocompatibility of central nervous system auditory prostheses.

As part of a program to determine the feasibility of a CNS auditory prosthesis, the tissue reaction to electrodes chronically implanted in the cochlear nucleus (CN) of the guinea pig was examined. Varied open operative approaches and microelectrode designs were utilized. Silicon substrate thin film and platinum-iridium wire electrodes, tethered and untethered, were placed successfully in different divisions of the CN. Implantation through a posterior suboccipital approach was most successful. Histologic examinations demonstrated a glial cell proliferation confined to the area of the electrode track that never exceeded 15 microns in width. No neuronal loss or significant effect on cell morphology was seen, and reactive cells were absent. Electrode migration was apparent in a minority of animal preparations. Although potential problems were identified, our findings lend support to the feasibility of implanting a neuroprosthesis in the CN and have helped to establish methods for future studies of chronic intranuclear stimulation.

Effect of electrical pulse shape on AVCN unit responses to cochlear stimulation.

Electrical stimulation of the cochlea with a multiple-electrode array is best accomplished using pulsatile instead of continuous stimulation. The optimum shapes of electrical pulses for this purpose are still uncertain due to a lack of knowledge about their stimulation efficiency and requirements of the encoding strategy. We presented an extensive set of charge-balanced, rectangular pulse shapes to the guinea pig cochlea. Durations per phase for these constant-current pulses ranged from 20 microseconds to 900 microseconds with initially positive and initially negative polarities. Spike counts from single units in the anteroventral cochlear nucleus differed significantly for different pulse shapes, as did their initial latencies. Implications for stimulation efficiency and encoding strategies are discussed.