Nature Biomedical EngineeringNeurosciencePeer-reviewed journal article
In vivo fluorescence imaging with a flat, lensless microscope
Jesse K. AdamsiD, Dong YaniD, Jimin WuiD, Vivek BoominathaniD, Sibo Gao, Alex V. Rodriguez, Soonyoung KimiD, Jennifer CarnsiD, Rebecca Rae Richards-KortumiD, Caleb T. KemereiD, Ashok VeeraraghavaniD, Jacob T. RobinsoniD
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Abstract
Fluorescence imaging over large areas of the brain in freely behaving animals would allow researchers to better understand the relationship between brain activity and behavior; however, traditional microscopes capable of high spatial resolution and large fields of view (FOVs) require large and heavy lenses that restrict animal movement. While lensless imaging has the potential to achieve both high spatial resolution and large FOV with a thin lightweight device, lensless imaging has yet to be achieved in vivo due to two principal challenges: (a) biological tissue typically has lower contrast than resolution targets, and (b) illumination and filtering must be integrated into this non-traditional device architecture. Here, we show that in vivo fluorescence imaging is possible with a thin lensless microscope by optimizing the phase mask and computational reconstruction algorithms, and integrating fiber optic illumination and thin-film color filters. The result is a flat, lensless imager that achieves better than 10 m spatial resolution and a FOV that is 30x larger than other cellular resolution miniature microscopes.
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