Skip to main content Accessibility help
×
Hostname: page-component-6bb9c88b65-9c7xm Total loading time: 0 Render date: 2025-07-25T13:07:48.376Z Has data issue: false hasContentIssue false

25 - CMOS technologiesfor retinal prosthesis

from Part V - Bionics

Published online by Cambridge University Press:  05 September 2015

Jun Ohta
Affiliation:
Nara Institute of Science and Technology (NIST)
Takashi Tokuda
Affiliation:
Nara Institute of Science and Technology (NIST)
Takashi Fujikado
Affiliation:
Osaka University
Sandro Carrara
Affiliation:
École Polytechnique Fédérale de Lausanne
Krzysztof Iniewski
Affiliation:
Redlen Technologies Inc., Canada
Get access

Summary

This chapter describes retinal prosthetic devices that are used withcomplementary metal oxide semiconductor (CMOS) technologies or large-scaleintegration (LSI) circuit technologies. The introduction of CMOStechnologies has made retinal prosthesis systems compact and versatile.Moreover, CMOS technology is particularly effective for increasing thenumber of stimulus electrodes with limited wiring. The remainder of thischapter is organized as follows. In Section 25.1, the principle of theretinal prosthesis and its basic components are discussed. In Section 25.2,various types of retinal prostheses are described. In Section 25.3, multiplemicrochip architectures that can realize a large number of stimuluselectrodes are introduced and demonstrated in detail. In Section 25.4integration of a photosensing function in a retinal stimulator is discussed.Finally, Section 25.5 proposes a smart electrode as an avenue for futureresearch in retinal prostheses. A preliminary demonstration isdescribed.

Principle and basic components of the retinal prosthesis

The front end of visual information is the retina. The human retina is athin, layered tissue with a thickness ranging from 0.1 to 0.4 mmattached to the inner surface of the eyeball [1], as shown in Figure 25.1.The retina has a layered structure with photoreceptor cells for lightdetection in the bottom layer and ganglion cells for output in the toplayer. The retina plays an important role in visual information collectionand processing, and so its dysfunction can result in blindness. Amongblindness diseases, retinitis pigmentosa (RP) and age-related maculardegeneration (AMD) have no effective remedies at present. In both cases, thephotoreceptors gradually become dysfunctional, so that the patienteventually becomes blind. However, some portion of ganglion cells remainsalive [2]. Consequently, by stimulating the remaining retinal cells, visualsensation or phosphenes can be evoked. This is the principle of the retinalprosthesis or artificial vision. Based on this principle, a retinalprosthetic device stimulates retinal cells with a patterned electricalsignal so that a blind patient can sense a phosphene pattern, or somethinglike an image. Stimulating the optic nerve and the visual cortex can alsorestore visual sensation, but this would require more complicated surgicaloperations.

Information

Type
Chapter
Information
Handbook of Bioelectronics
Directly Interfacing Electronics and Biological Systems
, pp. 313 - 324
Publisher: Cambridge University Press
Print publication year: 2015

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Book purchase

Temporarily unavailable

References

Wandell, B. A.. Foundations of Vision. Sunderland, MA:Sinauer Associates, Inc., 1995.Google Scholar
Santos, A., Humayun, M. S., de Juan, E., et al. “Preservation of the inner retina in retinitis pigmentosa. A morphometric analysis,” Arch. Ophthalmol. 115(4), 511–515, 1997.CrossRefGoogle ScholarPubMed
Ahuja, A. K., Dorn, J. D., Caspi, A., et al., “Blind subjects implanted with the Argus II retinal prosthesis are able to improve performance in a spatial-motor task,” Br. J. Ophthalmol., 95(4), 539–543, 2010.CrossRefGoogle Scholar
Richard, G., Keserue, M., Feucht, M., Post, N., Hornig, R., “Visual perception after long-term implantation of a retinal implant,” Invest. Opthalmol. Vis. Sci., 49, S1786, 2008.Google Scholar
Zrenner, E., Bartz-Schmidt, K. U., Benav, H., et al., “Subretinal electronic chips allow blind patients to read letters and combine them to words,” Proc. R. Soc. B, 278(1711), 1489–1497, 2011.CrossRefGoogle ScholarPubMed
Mathieson, K., Loudin, J., Goetz, G., et al., “Photovoltaic retinal prosthesis with high pixel density,” Nature Photon., 6, 391–397, 2012.CrossRefGoogle ScholarPubMed
Fujikado, T., Kamei, M., Sakaguchi, H., et al., “Testing of semichronically implanted retinal prosthesis by suprachoroidal-transretinal stimulation in patients with retinitis pigmentosa,” Invest. Ophthalmol. Vis. Sci., 52(7), 4726–4733, 2011.CrossRefGoogle ScholarPubMed
Chowdhury, V., Morley, J. W., Coroneo, M. T., “Development of an extraocular retinal prosthesis: evaluation of stimulation parameters in the cat,” J. Clin. Neurosci., 15(8), 900–906, 2008.CrossRefGoogle ScholarPubMed
Cha, K., Horch, K. W., Normann, R. A., “Mobility performance with a pixelized vision system,” Vision Res., 32(7), 1367–1372, 1988.CrossRefGoogle Scholar
Ohta, J., Tokuda, T., Kagawa, K., et al., “Laboratory investigation of microelectronics-based stimulators for large-scale suprachoroidal transretinal stimulation (STS),” J. Neural Eng., 4(1), S85–S91, 2007.CrossRefGoogle Scholar
Tokuda, T., Asano, R., Sugitani, S., et al., “Retinal stimulation on rabbit using CMOS-based multi-chip flexible stimulator toward retinal prosthesis,” Jpn. J. Appl. Phys. 47(4), 3220–3225, 2008.CrossRefGoogle Scholar
Chaia, X., Li, U., Wu, K., et al., “Optic nerve stimulation with penetrating electrode array,” IEEE Eng. Med. Biol. Mag., 27, 20–28, 2008.Google Scholar
Ohta, J., Tokuda, T., Kagawa, K., et al., “Silicon LSI-based smart stimulators for retinal prosthesis,” IEEE Eng. Med. Biol. Mag., 25(5), 47–59, 2006.CrossRefGoogle ScholarPubMed
Tokuda, T., Takeuchi, Y., Sagawa, Y., et al., “Development and in vivo demonstration of CMOS-based multichip retinal stimulator with simultaneous multisite stimulation capability,” IEEE Trans. Biomed. Circuits Systems, 4(6), 445–453, 2010.CrossRefGoogle ScholarPubMed
Tokuda, T., Hiyama, K., Sawamura, S., et al., “CMOS-based multichip networked flexible retinal stimulator designed for image-based retinal prosthesis,” IEEE Trans. Electron Devices, 56(11), 2577–2585, 2009.CrossRefGoogle Scholar
Noda, T., Sasagawa, K., Tokuda, T., et al., “A smart electrode array device with CMOS multi-chip architecture for neural interface,” Electron. Lett., 48(21), 1328–1329, 2012.CrossRefGoogle Scholar

Accessibility standard: Unknown

Accessibility compliance for the PDF of this book is currently unknown and may be updated in the future.

Save book to Kindle

To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×