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Artificial Human vision - KSOS

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426 Kerala Journal of Ophthalmology Vol. XXI, No. 4<br />

out with a new generation device having 49 electrodes.<br />

This trial named as the ‘Europe trial’ is going on in<br />

different universities in Europe including Hamburg,<br />

Parris, Austria, London. Reports of the out come can<br />

be expected by early next year.<br />

The project named EPI RET3 of Prof Walter et al. at<br />

University of Aachen reported results of a 25-electrode<br />

epiretinal array implanted for 4 weeks in 6 blind<br />

subjects 26 (Fig. 4).<br />

Fig.4. Camera chip embedded in goggle, epiretinal chip in<br />

position with stimulator in the posterior chamber.<br />

(image courtesy,IMI, Dr Hornig.)<br />

(ii) Subretinal Prostheses<br />

In the subretinal approach a micro photodiode array is<br />

implanted between the bipolar cell layer and the retinal<br />

pigment epithelium, either through an abexterno<br />

(scleral incision) or abinterno approach (through the<br />

vitreous cavity and retina).<br />

This was first described by Alan and Vincent Chow of<br />

Optobionics Corp, who believed that a subretinal<br />

implant could function as a simple solar cell without<br />

the need for a power or input source of any type 27,28,29 .<br />

Their <strong>Artificial</strong> Silicon Retina (ASR) Microchip is<br />

powered entirely by light entering the eye, without<br />

batteries or other ancillary devices. Two millimeters in<br />

diameter, the ASR contained approximately 5000<br />

microelectrode-tipped micro photodiodes which<br />

convert incident light into electrical signals similar to<br />

those normally produced by the retina’s own<br />

photoreceptors. These electrical impulses, in turn,<br />

stimulate any viable retinal neurons, which then process<br />

and send these signals to the visual processing centers<br />

in the brain via the optic nerve.This chip was implanted<br />

in 6 patients, with a follow-up of 6 to 18 months and<br />

reported gains in visual function in all patients as well<br />

as unexpected improvements in retinal areas distal to<br />

the implantation site. They hypothesized this as an<br />

effect due to the neuro modulation of the existing<br />

neurons due to the electrical activation.<br />

But later works demonstrated that the idea behind this<br />

simple approach is not feasible because it lacks a source<br />

of viable power 30 . Gabel et al showed that cortical<br />

activation secondary to retinal stimulation with such a<br />

device required brightness comparable to 2 to 3 times<br />

sunlight levels (energy) 31 . Simple photodiodes will also<br />

not produce charge balanced pulses, which are the<br />

safest form of electrical stimulation of nerve tissue. 32<br />

Across time, pulses that are not charge balanced will<br />

lead to dissolution of metal with toxicity to neural tissue<br />

and loss of electrode function. Methods to amplify these<br />

signals and produce charge balanced pulses are<br />

proposed but these add significantcomplexity 31 .<br />

In fact, Chow et al too have abandoned the notion that<br />

their ASR Microchip is efficacious as a prosthetic device<br />

and later thought that the low levels of current delivered<br />

from the implant, although insufficient to electrically<br />

activate any remaining retinal neurons in a retina with<br />

damaged photoreceptors, may act as therapeutic as well<br />

as neuro protective to otherwise dying retinal<br />

photoreceptors. Hence, it is thought that this type of<br />

an implant works through a “growth factor” that then<br />

rescues the remaining photoreceptors. Thus, some of<br />

the researchers claimed that this device is not a true<br />

retinal prosthesis but should be best classified as a<br />

therapeutic device.Studies by Pardue et al were on to<br />

determine whether these effects are indeed neuro<br />

protective as well as if they are persisting and<br />

reproducible 33, 34 . In addition, studies are also ongoing<br />

to determine whether an electronically inactive implant<br />

can have similar effects.<br />

In Germany another design for a subretinal implant<br />

has been under development since 1996 by a<br />

consortium of research universities under the guidance<br />

of Eberhart Zrenner. They have demonstrated in various<br />

animal models with comparable retinal degenerations<br />

that subretinal stimulation elicits neuronal activity in<br />

retinal ganglion cells. Also they were successful in<br />

defining parameters necessary for successful electric<br />

stimulation and then incorporated these data into the<br />

development of their photodiode arrays 35,36 .<br />

Having identified that the subretinal approach to a<br />

retinal prosthesis is not practical without an additional

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