Metasurface-based super-resolution image scanning microscopy

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초록

Image scanning microscopy (ISM) enhances optical resolution by applying pixel reassignment. A large number of evenly generated focal points is essential for this method, as it involves scanning a multifocal array. Historically, multifocal arrays have been produced using electronically controlled optical modulators such as digital micromirror devices (DMDs) or microlens arrays. However, electronic modulators can be cost-inefficient and require intricate alignment, while microlens arrays often demand a lengthy optical path for demagnification and have limited numerical aperture, resulting in bulky systems that are challenging to align and maintain. In this work, we introduce a novel multifocal metalens design capable of providing a dense and uniform distribution of focal points to enable ISM. Metalenses, constructed from regularly arranged nanostructures, offer ultrathin profiles and versatile optical modulation functions. As a proof of concept, we developed an ISM system using our multifocal metalens and successfully captured super-resolution images of neurons in brain organoids. We anticipate that our method will guide the creation of advanced, streamlined optical microscopes based on metalens technology. © 2025 SPIE.

키워드

biological imagingbrain organoidhigh NAimage scanning microscopeMetalensmultifocusneuronsuper-resolution
제목
Metasurface-based super-resolution image scanning microscopy
저자
Jo, YongjaePark, HyemiLee, SehoYoon, HyeyoungLee, TaehoonBak, Gyu SooPark, Jong-ChanKim, Inki
DOI
10.1117/12.3040456
발행일
2025-03
유형
Proceedings Paper
저널명
Progress in Biomedical Optics and Imaging - Proceedings of SPIE
13340