Evidence map›Paper›PMID 35810324›Full record

ArticleJournal of biomedical optics2022

In vivo accurate detection of the liver tumor with pharmacokinetic parametric images from dynamic fluorescence molecular tomography.

Fei Liu, Peng Zhang, Zeyu Liu, Fan Song, Chenbin Ma, Yangyang Sun, Youdan Feng, Yufang He, Guanglei Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2022. 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
1.0field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Quantitative imaging in medicine and surgery · 2023
    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

9 authors at 2 institutions in 1 country.

Fei LiuBeijing Information Science & Technology University, Advanced Information and Industrial Technology, China.
Peng ZhangBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Zeyu LiuBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Fan SongBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Chenbin MaBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Yangyang SunBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Youdan FengBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Yufang HeBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Guanglei ZhangBeihang University, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biologi, China.
Beihang University · CNBeijing Information Science & Technology University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

significancePharmacokinetic parametric images in dynamic fluorescence molecular tomography (FMT) can describe three-dimensional (3D) physiological and pathological information inside biological tissues, potentially providing quantitative assessment tools for biological research and drug development.

aimIn vivo imaging of the liver tumor with pharmacokinetic parametric images from dynamic FMT based on the differences in metabolic properties of indocyanine green (ICG) between normal liver cells and tumor liver cells inside biological tissues. APPROACH: First, an orthotopic liver tumor mouse model was constructed. Then, with the help of the FMT/computer tomography (CT) dual-modality imaging system and the direct reconstruction algorithm, 3D imaging of liver metabolic parameters in nude mice was achieved to distinguish liver tumors from normal tissues. Finally, pharmacokinetic parametric imaging results were validated against in vitro anatomical results.

resultsThis letter demonstrates the ability of dynamic FMT to monitor the pharmacokinetic delivery of the fluorescent dye ICG in vivo, thus, enabling the distinction between normal and tumor tissues based on the pharmacokinetic parametric images derived from dynamic FMT.

conclusionsCompared with CT structural imaging technology, dynamic FMT combined with compartmental modeling as an analytical method can obtain quantitative images of pharmacokinetic parameters, thus providing a more powerful research tool for organ function assessment, disease diagnosis and new drug development.

Indexed as

Liver NeoplasmsTomographyAnimalsFluorescent DyesHep G2 CellsHumansImage Processing, Computer-AssistedMiceMice, NudeNeoplasm TransplantationFluorescent Dyesdynamic fluorescence tomographyliver tumor detectionpharmacokinetic imaging

Identifiers

PMID35810324
PMCPMC9270690
OpenAlexW4284964719

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.