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Bionic eye for treating blindness

by Nigel Lovell
  This silicon chip, encapsulated in ceramic and with a 100-wire electrode array attached, is to be surgically implanted in the eyeball. The whole device is about the size of a five-cent piece.
 
This silicon chip, encapsulated in ceramic and with a 100-wire electrode array attached, is to be surgically implanted in the eyeball. The whole device is about the size of a five-cent piece.

A joint research team led by UNSW’s Associate Professor Nigel Lovell and the University of Newcastle’s Dr Gregg Suaning, has taken major steps towards producing a bionic eye for the treatment of blindness, with the development of a silicon chip that replaces the sensory part of the eye — the retina.

The chip would be implanted inside the body and connected into the nervous system through miniature platinum electrodes. The device receives signals from a pair of glasses fitted with a camera and worn by the patient.

The camera feeds the visual information into a separate imageprocessing unit, which makes ‘sense’ of the image by extracting certain features. It might find a door, for example, by contrasting the bright open door with a dark room.

The unit then breaks down the image into pixels and sends the information, one pixel at a time, to the implanted silicon chip, which then reconstructs the image. Electronic impulses from the chip are used to stimulate 100 unique sites on the retina. It is hoped these excited nerves will send signals to the brain to give the sensation of sight.

The chip also includes a two-way radio communication system that allows visual perceptions. However, whether these perceptions could be interpreted in the human brain as useful vision remains to be shown. The team is now looking towards short-term testing in human patients in 2003. If the trials are successful, a commercially available device would still be five to ten years away.

Likely candidates for future ‘bionic eye’ technology would be people with progressive eye diseases that lead to loss of vision, like retinitis pigmentosa and age-related macular degeneration, but who were born with vision and therefore have the necessary brain pathways established for processing visual information, unlike those who were born blind.

For further information, please contact Associate Professor Nigel Lovell at N.Lovell@unsw.edu.au or visit the website at bionic.gsbme.unsw.edu.au

 

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