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Lab-on-a-chip device mimics eye damage due to intense light

Researchers create eye neuron network model to study retinal diseases, possible treatment options…

Researchers have developed a new lab-on-a-chip technology that could quickly screen possible drugs to repair damaged neuron and retinal connections, like what is seen in people with macular degeneration or who’ve had too much exposure to the glare of electronic screens.

Researchers led by Houston Methodist Research Institute nanomedicine faculty member Dr Lidong Qin, explain how they created a sophisticated retina cell network on a chip that is modelled after a human’s neural network. This will further the quest for finding the right drug to treat such retinal diseases.

Light damaged retina cone photoreceptors will spread the death signal to neighbour cells and cause irrevocable hurts in a 24-hour period. (Houston Methodist).

“Medical treatments have advanced but there is still no perfect drug to cure any one of these diseases. Our device can screen drugs much faster than previous technologies. With the new technology and a few years’ effort, the potential to develop a new drug is highly possible,” said Dr Qin.

Named the NN-Chip, the high-throughput platform consists of many channels that can be tailored to imitate large brain cell networks as well as focus on individual neural cells, such as those found in the retina. Using extremely bright light to selectively damage retina photoreceptors in the device, they discovered the damaged cells are not only difficult to recover but also cause neighbouring cells to quickly die.

“This so-called ‘bystander killing effect’ in retina cone photoreceptors leads us to believe that once retina cells are severely damaged, the killing effect will spread to other healthy cells which can cause irrevocable damage,” said Dr Qin. “What surprised us was how quickly the killing effect progressed in the experimental model. The damage went from 100 cells to 10, 000 cells in 24 hours.”

The NN-Chip is an improvement on Dr Qin’s BloC-Printing technology, which allowed researchers to print living cells onto any surface in any shape within the confines of a mould. With this latest iteration, Dr Qin’s lab loaded and tested cells with micro-needles in an open dish so they could tailor the neural network device, study individual cells as well as the progression of drugs through the platform’s many channels.

Retinal degeneration is a leading cause of blindness that, together with glaucoma, retinitis pigmentosa, and age-related macular degeneration, will affect 196 million people worldwide in 2020.

Dr Qin hopes the platform will have additional applications in creating models for Huntington’s and Alzheimer’s diseases and screening therapeutic drugs.

In research appears in the journal Science Advances.

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