Evidence map›Paper›PMID 29138489›Full record

ArticleScientific reports2017

A dual-channel endoscope for quantitative imaging, monitoring, and triggering of doxorubicin release from liposomes in living mice.

Jeremy Kress, Daniel J Rohrbach, Kevin A Carter, Dandan Luo, Chien Poon, Semra Aygun-Sunar, Shuai Shao, Shashikant Lele, Jonathan F Lovell, Ulas Sunar

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. Review of structured light in diffuse optical imaging.Journal of biomedical optics · 2018
    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

10 authors.

Jeremy KressDepartment of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA.
Daniel J RohrbachDepartment of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA.
Kevin A CarterDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA.
Dandan LuoDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA.
Chien PoonDepartment of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA.
Semra Aygun-SunarDepartment of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA.
Shuai ShaoDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA.
Shashikant LeleDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Jonathan F LovellDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY, USA.
Ulas SunarDepartment of Biomedical, Industrial & Human Factors Engineering, Wright State University, Dayton, OH, USA. ulas.sunar@wright.edu.ORCID 0000-0002-0623-7522

Funding

Quantitative Endoscopic Imaging and Structured Light Delivery for Controlled DrugR21EB019147 · NIBIB · WRIGHT STATE UNIVERSITY · PI SUNAR, ULAS · 2014 to 2015
$412k
NIBIB NIH HHS R21 EB019147
6 · The paper itself

Abstract

Doxorubicin (Dox) is approved for use in liposomal form for the treatment of ovarian cancer. We previously developed a long-circulating Dox formulation in liposomes containing small amounts of porphyrin-phospholipid, which enables on-demand drug release with near-infrared irradiation. In this study, we present and evaluate a dual-modal, dual-channel light endoscope that allows quantitative reflectance and fluorescence imaging for monitoring of local Dox concentrations in target areas. The endoscope consists of two flexible imaging fibers; one to transmit diagnostic and therapeutic light to the target, and the other to detect fluorescent and reflected light. Thus, the endoscope serves for imaging, for light delivery to trigger drug release, and for monitoring drug concentration kinetics during drug release. We characterized the performance of this endoscope in tissue phantoms and in an in vivo model of ovarian cancer. This study demonstrates the feasibility of non-invasive, quantitative mapping of Dox distribution in vivo via endoscopic imaging.

Indexed as

EndoscopesAnimalsDiagnostic ImagingDoxorubicinDrug Delivery SystemsDrug LiberationFemaleHumansKineticsLiposomesMiceOvarian NeoplasmsDoxorubicinLiposomes

Identifiers

PMID29138489
PMCPMC5686102

What OpenQuestion holds

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LicenceCC BY
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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.