Evidence map›Paper›PMID 36745734›Full record

ArticleACS nano2023

Rapid Cellular-Resolution Skin Imaging with Optical Coherence Tomography Using All-Glass Multifocal Metasurfaces.

Jingjing Zhao, Aidan Van Vleck, Yonatan Winetraub, Lin Du, Yong Han, Sumaira Aasi, Kavita Yang Sarin, Adam de la Zerda

Abstract read
In one paragraph

Article in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

8 authors.

Jingjing ZhaoDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California94305, United States.ORCID 0000-0003-0937-2751
Aidan Van VleckDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California94305, United States.
Yonatan WinetraubDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California94305, United States.
Lin DuDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, 94720, United States.
Yong HanDepartment of Precision Instrument, Tsinghua University, Beijing100084, China.
Sumaira AasiDepartment of Dermatology, Stanford University School of Medicine, Stanford, California94305, United States.
Kavita Yang SarinDepartment of Dermatology, Stanford University School of Medicine, Stanford, California94305, United States.
Adam de la ZerdaDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California94305, United States.

Funding

Pilot ProjectsU54CA151459 · NCI · STANFORD UNIVERSITY · PI SINCLAIR, ROBERT · 2010 to 2014
$12.6M
Repurposing systemic therapies to improve clinical outcomes in advanced basal cell cancerK23CA211793 · NCI · STANFORD UNIVERSITY · PI SARIN, KAVITA YANG · 2018 to 2022
$868k
NCI NIH HHS K23 CA211793NCI NIH HHS U54 CA151459
6 · The paper itself

Abstract

Cellular-resolution optical coherence tomography (OCT) is a powerful tool offering noninvasive histology-like imaging. However, like other optical microscopy tools, a high numerical aperture (N.A.) lens is required to generate a tight focus, generating a narrow depth of field, which necessitates dynamic focusing and limiting the imaging speed. To overcome this limitation, we developed a metasurface platform that generates multiple axial foci, which multiplies the volumetric OCT imaging speed by offering several focal planes. This platform offers accurate and flexible control over the number, positions, and intensities of axial foci generated. All-glass metasurface optical elements 8 mm in diameter are fabricated from fused-silica wafers and implemented into our scanning OCT system. With a constant lateral resolution of 1.1 μm over all depths, the multifocal OCT triples the volumetric acquisition speed for dermatological imaging, while still clearly revealing features of stratum corneum, epidermal cells, and dermal-epidermal junctions and offering morphological information as diagnostic criteria for basal cell carcinoma. The imaging speed can be further improved in a sparse sample, e.g., 7-fold with a seven-foci beam. In summary, this work demonstrates the concept of metasurface-based multifocal OCT for rapid virtual biopsy, further providing insights for developing rapid volumetric imaging systems with high resolution and compact volume.

Indexed as

SkinTomography, Optical CoherenceEpidermal CellsMicroscopyall-glass metasurfacecellular resolutionmultifocal beamnoninvasive imagingoptical coherence tomographyphase change materialsvirtual biopsy

Identifiers

PMID36745734
PMCPMC10619470

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Registered trials

None linked

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.