Evidence map›Paper›PMID 34567682›Full record

ArticleMicrosystems & nanoengineering2020

Handheld endomicroscope using a fiber-optic harmonograph enables real-time and in vivo confocal imaging of living cell morphology and capillary perfusion.

Kyungmin Hwang, Yeong-Hyeon Seo, Daniel Y Kim, Jinhyo Ahn, Soyoung Lee, Kyung Hee Han, Koun-Hee Lee, Sangyong Jon, Pilhan Kim, Kate E Yu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microsystems & nanoengineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 33 citations in OpenAlex.

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  5. Motion Blur Microscopy.bioRxiv : the preprint server for biology · 2024
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  7. Review
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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

13 authors at 4 institutions in 4 countries.

Kyungmin HwangDepartment of Bio and Brain Engineering, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.
Yeong-Hyeon SeoDepartment of Bio and Brain Engineering, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.
Daniel Y KimDepartment of Bio and Brain Engineering, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.
Jinhyo AhnGraduate School of Nanoscience and Technology, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.
Soyoung LeeDepartment of Biological Sciences, KAIST and KAIST Institute for the BioCentury, Daejeon, 34141 Republic of Korea.
Kyung Hee HanHyunjoo In-Tech, Seoul, 08390 Republic of Korea.
Koun-Hee LeeVPIX Medical, Inc, Deajeon, 34141 Republic of Korea.
Sangyong JonDepartment of Biological Sciences, KAIST and KAIST Institute for the BioCentury, Daejeon, 34141 Republic of Korea.ORCID 0000-0002-6971-586X
Pilhan KimGraduate School of Nanoscience and Technology, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.
Kate E YuVPIX Medical, Inc, Deajeon, 34141 Republic of Korea.
Hyungsin KimDepartment of Neurosurgery, Korea University Anam Hospital, Korea University Medicine, Seoul, 02842 Korea.
Shin-Hyuk KangDepartment of Neurosurgery, Korea University Anam Hospital, Korea University Medicine, Seoul, 02842 Korea.
Ki-Hun JeongDepartment of Bio and Brain Engineering, KAIST and KAIST Institute of Health Science and Technology, Daejeon, 34141 Republic of Korea.ORCID 0000-0003-4799-7816
Korea Advanced Institute of Science and Technology · KRKorea University Medical Center · KRTiGenix (Spain) · ESHyper Tech Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Confocal laser endomicroscopy provides high potential for noninvasive and in vivo optical biopsy at the cellular level. Here, we report a fully packaged handheld confocal endomicroscopic system for real-time, high-resolution, and in vivo cellular imaging using a Lissajous scanning fiber-optic harmonograph. The endomicroscopic system features an endomicroscopic probe with a fiber-optic harmonograph, a confocal microscope unit, and an image signal processor. The fiber-optic harmonograph contains a single mode fiber coupled with a quadrupole piezoelectric tube, which resonantly scans both axes at ~ 1 kHz to obtain a Lissajous pattern. The fiber-optic harmonograph was fully packaged into an endomicroscopic probe with an objective lens. The endomicroscopic probe was hygienically packaged for waterproofing and disinfection of medical instruments within a 2.6-mm outer diameter stainless tube capable of being inserted through the working channel of a clinical endoscope. The probe was further combined with the confocal microscope unit for indocyanine green imaging and the image signal processor for high frame rate and high density Lissajous scanning. The signal processing unit delivers driving signals for probe actuation and reconstructs confocal images using the auto phase matching process of Lissajous fiber scanners. The confocal endomicroscopic system was used to successfully obtain human in vitro fluorescent images and real-time ex vivo and in vivo fluorescent images of the living cell morphology and capillary perfusion inside a single mouse.

Indexed as

Electrical and electronic engineeringEnvironmental, health and safety issuesOptical sensors

Identifiers

PMID34567682
PMCPMC8433427
OpenAlexW3094393938

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.