Evidence map›Paper›PMID 29232054›Full record

ArticleJournal of biophotonics2018

High-speed microscopy for in vivo monitoring of lymph dynamics.

Mustafa Sarimollaoglu, Amanda J Stolarz, Dmitry A Nedosekin, Brittney R Garner, Terry W Fletcher, Ekaterina I Galanzha, Nancy J Rusch, Vladimir P Zharov

Abstract read
In one paragraph

Article in Journal of biophotonics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  8. KThe Journal of pharmacology and experimental therapeutics · 2021
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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

8 authors at 1 institution in 1 country.

Mustafa SarimollaogluArkansas Nanomedicine Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Amanda J StolarzDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Dmitry A NedosekinArkansas Nanomedicine Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Brittney R GarnerDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Terry W FletcherDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Ekaterina I GalanzhaArkansas Nanomedicine Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Nancy J RuschDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Vladimir P ZharovArkansas Nanomedicine Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
University of Arkansas for Medical Sciences · US

Funding

In vivo real-time detection of circulating melanoma cellsR01CA131164 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI SUEN, JAMES · 2009 to 2019
$3.1M
Systems Pharmacology and Toxicology Training ProgramT32GM106999 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI PRATHER, PAUL L · 2013 to 2022
$1.4M
Photoswitchable nanoprobes for in vivo flow cytometryR01EB017217 · NIBIB · UNIV OF ARKANSAS FOR MED SCIS · PI ZHAROV, VLADIMIR P · 2014 to 2017
$1.3M
Interaction of gold nanoparticles with lymphatic vesselsR21EB022698 · NIBIB · UNIV OF ARKANSAS FOR MED SCIS · PI GALANZHA, EKATERINA I. · 2016 to 2017
$398k
Doxorubicin suppression of lymphatic function and therapeutic reversalR21CA187325 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI RUSCH, NANCY J · 2015 to 2016
$353k
Lymph liquid biopsy in cancerR21CA230059 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI GALANZHA, EKATERINA I. · 2018 to 2019
$344k
NCI NIH HHS R01 CA131164NCI NIH HHS R21 CA187325NCI NIH HHS R21 CA230059NIBIB NIH HHS R01 EB017217NIBIB NIH HHS R21 EB022698NIGMS NIH HHS T32 GM106999
6 · The paper itself

Abstract

The lymphatic system contributes to body homeostasis by clearing fluid, lipids, plasma proteins and immune cells from the interstitial space. Many studies have been performed to understand lymphatic function under normal conditions and during disease. Nevertheless, a further improvement in quantification of lymphatic behavior is needed. Here, we present advanced bright-field microscopy for in vivo imaging of lymph vessels (LVs) and automated quantification of lymphatic function at a temporal resolution of 2 milliseconds. Full frame videos were compressed and recorded continuously at up to 540 frames per second. A new edge detection algorithm was used to monitor vessel diameter changes across multiple cross sections, while individual cells in the LVs were tracked to estimate flow velocity. The system performance initially was verified in vitro using 6- and 10-μm microspheres as cell phantoms on slides and in 90-μm diameter tubes at flow velocities up to 4 cm/second. Using an in vivo rat model, we explored the mechanisms of lymphedema after surgical lymphadenectomy of the mesentery. The system revealed reductions of mesenteric LV contraction and flow rate. Thus, the described imaging system may be applicable to the study of lymphatic behavior during therapeutic and surgical interventions, and potentially during lymphatic system diseases.

Indexed as

AnimalsImage Processing, Computer-AssistedLymphatic VesselsMaleMicroscopyRatsRats, Sprague-DawleyTime Factorscell trackingcontractiondiameter trackingedge detectionimaginglymphlymphedemalymph flowvideo microscopy

Identifiers

PMID29232054
PMCPMC6314807
OpenAlexW2771626534

What OpenQuestion holds

Textmetadata
LicenceTDM
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.