Evidence map›Paper›PMID 32860356›Full record

ArticleJournal of biomedical optics2020

Pharmacokinetic characterization of fluorocoxib D, a cyclooxygenase-2-targeted optical imaging agent for detection of cancer.

Maria Cekanova, Sony Pandey, Shelly Olin, Phillip Ryan, Jennifer E Stokes, Silke Hecht, Tomas Martin-Jimenez, Md Jashim Uddin, Lawrence J Marnett

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Maria CekanovaThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Sony PandeyThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Shelly OlinThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Phillip RyanThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Jennifer E StokesThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Silke HechtThe University of Tennessee, College of Veterinary Medicine, Department of Small Animal Clinical Sci, United States.
Tomas Martin-JimenezThe University of Tennessee, College of Veterinary Medicine, Department of Biomedical and Diagnostic, United States.
Md Jashim UddinVanderbilt University School of Medicine, Vanderbilt Institute of Chemical Biology, Center for Molec, United States.
Lawrence J MarnettVanderbilt University School of Medicine, Vanderbilt Institute of Chemical Biology, Center for Molec, United States.
University of Tennessee at Knoxville · USVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

significanceFluorocoxib D, N-[(rhodamin-X-yl)but-4-yl]-2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetamide, is a water-soluble optical imaging agent to detect cyclooxygenase-2 (COX-2)-expressing cancer cells.

aimWe evaluated the pharmacokinetic and safety properties of fluorocoxib D and its ability to detect cancer cells in vitro and in vivo. APPROACH: Pharmacokinetic parameters of fluorocoxib D were assessed from plasma collected at designated time points after intravenous administration of 1  mg  /  kg fluorocoxib D in six research dogs using a high-performance liquid chromatography analysis. Safety of fluorocoxib D was assessed for 3 days after its administration using physical assessment, complete blood count, serum chemistry profile, and complete urinalysis in six research dogs. The ability of fluorocoxib D to detect COX-2-expressing cancer cells was performed using human 5637 cells in vitro and during rhinoscopy evaluation of specific fluorocoxib D uptake by canine cancer cells in vivo.

resultsNo evidence of toxicity and no clinically relevant adverse events were noted in dogs. Peak concentration of fluorocoxib D (114.8  ±  50.5  ng  /  ml) was detected in plasma collected at 0.5 h after its administration. Pretreatment of celecoxib blocked specific uptake of fluorocoxib D in COX-2-expressing human 5637 cancer cells. Fluorocoxib D uptake was detected in histology-confirmed COX-2-expressing head and neck cancer during rhinoscopy in a client-owned dog in vivo. Specific tumor-to-normal tissue ratio of detected fluorocoxib D signal was in an average of 3.7  ±  0.9 using Image J analysis.

conclusionsOur results suggest that fluorocoxib D is a safe optical imaging agent used for detection of COX-2-expressing cancers and their margins during image-guided minimally invasive biopsy and surgical procedures.

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsCyclooxygenase 2Cyclooxygenase 2 InhibitorsDogsOptical ImagingAntineoplastic AgentsCyclooxygenase 2Cyclooxygenase 2 Inhibitorsbiopsycyclooxygenase-2dog with naturally occurring cancerfluorocoxiboptical imagingpharmacokinetic parameters

Identifiers

PMID32860356
PMCPMC7456637
OpenAlexW3082160633

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.