Evidence map›Paper›PMID 41306990›Full record

ArticleBiomedical optics express2025

Silicon nitride PIC beam formers for light sheet fluorescent microscopy.

Alireza Tabatabaei Mashayekh, Jeremy Witzens

Abstract read
In one paragraph

Article in Biomedical optics express, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Alireza Tabatabaei MashayekhInstitute of Integrated Photonics, RWTH Aachen University, Campus Boulevard 73, 52074 Aachen, Germany.ORCID https://orcid.org/0009-0003-8982-3301
Jeremy WitzensInstitute of Integrated Photonics, RWTH Aachen University, Campus Boulevard 73, 52074 Aachen, Germany.ORCID https://orcid.org/0000-0002-2896-7243

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Light sheet fluorescence microscopy (LSFM) has transformed the way we visualize biological tissues in three dimensions, offering high-resolution imaging while minimizing photo-induced damage to the samples. Recent breakthroughs in tissue-clearing methods have further improved LSFM's capabilities, making it possible to study larger, intact samples in unprecedented detail. To overcome limitations like shallow penetration and light diffraction in traditional LSFM setups, advanced beam shaping with devices such as spatial light modulators and digital micromirror arrays has been utilized. These improve the resolution and the extent of tissues that can be imaged. Advances such as Bessel-beam-based LSFM and lattice light sheet microscopy increase the field of view that can be imaged with low background noise, but often require complex and bulky equipment. Addressing these complexities, a new approach builds on silicon nitride photonic integrated circuits to create a structured light sheet in a very compact device. This system incorporates beam-steering based on wavelength control in a limited tuning range and enables the generation of light sheets with optimized characteristics in regard to thickness and diffraction-length-limited penetration depth. Simulations include extensive fabrication tolerance analysis that confirms the practicability of the approach, which can be straightforwardly extended to dual wavelength excitation. This compact, chip-based LSFM system could make high-quality imaging more accessible and transform biomedical instrumentation.

Identifiers

PMID41306990
PMCPMC12646048

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.