Evidence map›Paper›PMID 25955381›Full record

ArticleJournal of chromatography. B, Analytical technologies in the biomedical and life sciences2015

A liquid chromatography with tandem mass spectrometry method for simultaneous determination of UTL-5g and its metabolites in human plasma.

Jiajiu Shaw, Richard Wiegand, Jianmei Wu, Xun Bao, Frederick Valeriote, Jing Li

Abstract readValidation Study
In one paragraph

Article in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2015. 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
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.

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

6 authors.

Jiajiu Shaw21st Century Therapeutics, Inc., 440 Burroughs, Suite 447 Detroit, MI 48202, United States. Electronic address: jiajiushaw@gmail.com.
Richard WiegandKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, United States.
Jianmei WuKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, United States.
Xun BaoKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, United States.
Frederick ValerioteHenry Ford Health System, Internal Medicine, Detroit, MI 48202, United States.
Jing LiKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, United States. Electronic address: lijin@karmanos.org.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Novel small-molecule TNF-a modulators as chemoprotective agentsR44CA141749 · NCI · 21ST CENTURY THERAPEUTICS, INC. · PI SHAW, JIAJIU · 2011 to 2012
$1.1M
NCI NIH HHS 2R44CA141749-02NCI NIH HHS P30 CA022453NCI NIH HHS R44 CA141749
6 · The paper itself

Abstract

UTL-5g is a novel small-molecule TNF-α inhibitor under investigation as both a chemoprotective and radioprotective agent. Animal studies showed that pretreatment of UTL-5g protected kidney, liver, and platelets from cisplatin-induced toxicity. In addition, UTL-5g reduced liver and lung injuries induced by radiation in vivo. Although a number of preclinical studies have been conducted, a validated bioanalytical method for UTL-5g in human plasma has not been published. In this work, a sensitive and reproducible reverse-phase liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) assay was developed and validated for the determination of UTL-5g and its metabolites, 5-methylisoxazole-3-carboxylic acid (ISOX) and 2,4-dichloroaniline (DCA), in human plasma. The method involves a simple methanol precipitation step followed by injection of the supernatant onto a Waters 2695 HPLC system coupled with a Waters Quattro Micro™ triple quadrupole mass spectrometer. Chromatographic separation was accomplished using a Waters Nova-Pak C18 column maintained at 30°C, running at gradient mode with mobile phase consisting of 0.1% formic acid in water and 0.1% formic acid in methanol at a flow rate of 0.2mL/min. The analytes were monitored under positive electrospray ionization (ESI). Quantitation of these compounds in plasma was linear from 0.05 to 10μM. The lower limit of quantitation (LLOQ) was 0.05, 0.1, and 0.2μM for UTL-5g, ISOX and DCA, respectively. The accuracy and intra-and inter-day precisions were within the generally accepted criteria for bioanalytical method (<15%). This method provides a practical tool to measure and characterize the plasma concentration-time profiles for UTL-5g and its metabolites, ISOX and DCA.

Indexed as

Aniline CompoundsChromatography, Reverse-PhaseHumansIsoxazolesLimit of DetectionTandem Mass SpectrometryTumor Necrosis Factor-alpha2,4-dichloroanilineAniline CompoundsIsoxazolesTNF protein, humanTumor Necrosis Factor-alphaUTL-5g compoundBioanalytical method validationLC–MS/MSUTL-5g

Identifiers

PMID25955381
PMCPMC6902638

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.