Ceramic-based microelectrode arrays: Recording surface characteristics and topographical analysis

Pooja M. Talauliker, David A. Price, Jason J. Burmeister, Silpa Nagari, Jorge E. Quintero, Francois Pomerleau, Peter Huettl, J. Todd Hastings, Greg A. Gerhardt

Producción científica: Articlerevisión exhaustiva

16 Citas (Scopus)

Resumen

Amperometric measurements using microelectrode arrays (MEAs) provide spatially and temporally resolved measures of neuromolecules in the central nervous system of rats, mice and non-human primates. Multi-site MEAs can be mass fabricated on ceramic (Al2O3) substrate using photolithographic methods, imparting a high level of precision and reproducibility in a rigid but durable recording device. Although the functional capabilities of MEAs have been previously documented for both anesthetized and freely moving paradigms, the performance enabling intrinsic physical properties of the MEA device have not heretofore been presented. In these studies, spectral analysis confirmed that the MEA recording sites were primarily composed of elemental platinum (Pt°). In keeping with the precision of the photolithographic process, scanning electron microscopy revealed that the Pt recording sites have unique microwell geometries post-fabrication. Atomic force microscopy demonstrated that the recording surfaces have nanoscale irregularities in the form of elevations and depressions, which contribute to increased current per unit area that exceeds previously reported microelectrode designs. The ceramic substrate on the back face of the MEA was characterized by low nanoscale texture and the ceramic sides consisted of an extended network of ridges and cavities. Thus, individual recording sites have a unique Pt° composition and surface profile that has not been previously observed for Pt-based microelectrodes. These features likely impact the physical chemistry of the device, which may influence adhesion of biological molecules and tissue as well as electrochemical recording performance post-implantation. This study is a necessary step towards understanding and extending the performance abilities of MEAs in vivo.

Idioma originalEnglish
Páginas (desde-hasta)222-229
Número de páginas8
PublicaciónJournal of Neuroscience Methods
Volumen198
N.º2
DOI
EstadoPublished - jun 15 2011

Nota bibliográfica

Funding Information:
We thank Larry Rice and George Turpin (University of Kentucky Electron Microscopy Center, Lexington, KY) for their assistance with data processing. This work was supported by grants from USPHS NS39787, DA017186, AG13494, T32 AG000242 and NSF EEC-0310723.

Financiación

We thank Larry Rice and George Turpin (University of Kentucky Electron Microscopy Center, Lexington, KY) for their assistance with data processing. This work was supported by grants from USPHS NS39787, DA017186, AG13494, T32 AG000242 and NSF EEC-0310723.

FinanciadoresNúmero del financiador
National Science Foundation Arctic Social Science ProgramEEC-0310723
National Science Foundation Arctic Social Science Program
National Institute on Drug AbuseR01DA017186
National Institute on Drug Abuse
U.S. Public Health ServiceAG13494, T32 AG000242, NS39787, DA017186
U.S. Public Health Service

    ASJC Scopus subject areas

    • General Neuroscience

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