Evidence map›Paper›PMID 28284083›Full record

ArticleJournal of pharmaceutical and biomedical analysis2017

Plasma pharmacokinetics and bioavailability of verticillin A following different routes of administration in mice using liquid chromatography tandem mass spectrometry.

Jiang Wang, Xiaohua Zhu, Shamala Kolli, Hongyan Wang, Cedric J Pearce, Nicholas H Oberlies, Mitch A Phelps

Abstract read
In one paragraph

Article in Journal of pharmaceutical and biomedical analysis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Melinacidin-ProducingPathogens (Basel, Switzerland) · 2021
    Article
  5. 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

7 authors at 3 institutions in 1 country.

Jiang WangComprehensive Cancer Center, The Ohio State University, Columbus, OH, United States.
Xiaohua ZhuCollege of Pharmacy, The Ohio State University, Columbus, OH, United States.
Shamala KolliComprehensive Cancer Center, The Ohio State University, Columbus, OH, United States.
Hongyan WangComprehensive Cancer Center, The Ohio State University, Columbus, OH, United States.
Cedric J PearceMycosynthetix, Inc., 505 Meadowlands Dr., Suite 103, Hillsborough, NC 27278, United States.
Nicholas H OberliesDepartment of Chemistry & Biochemistry, University of North Carolina at Greensboro, P.O. Box 26170, Greensboro, NC 27402, United States.
Mitch A PhelpsComprehensive Cancer Center, The Ohio State University, Columbus, OH, United States; College of Pharmacy, The Ohio State University, Columbus, OH, United States. Electronic address: phelps.32@osu.edu.
The Ohio State University · USMycosynthetix (United States) · USUniversity of North Carolina at Greensboro · US

Funding

Project 3:Isolation Chemistry of Filamentous Fungi and Biological EvaluationP01CA125066 · NCI · OHIO STATE UNIVERSITY · PI JAMES R FUCHS · 2007 to 2026
$27.2M
NCI NIH HHS P01 CA125066
6 · The paper itself

Abstract

Verticillin A is a natural product isolated from fungal cultures and has displayed potent antibiotic, antiviral, nematocidal, and anticancer properties in vitro. While in vivo studies have been limited due to sparse supply, the in vivo efficacy data that does exist demonstrates potent anti-tumor activity in murine cancer models. The current study aims to investigate the pharmacokinetics and bioavailability of verticillin A in mice to provide guidance for further efficacy assessment in mouse models. A sensitive and specific liquid chromatography-tandem mass spectrometry method was developed and validated for the quantification of verticillin A in mouse plasma. Sample preparation was accomplished through protein precipitation, and chromatographic separation was achieved on an Agilent Zorbax Extend C18 column with a security guard cartridge C8 using a binary gradient with mobile phase A (water/0.1% formic acid) and B (ACN/0.1% formic acid) at a flow rate of 400μl/min. Elution of verticillin A and internal standard, hesperetin, occurred at 4.87 and 2.06min, respectively. The total chromatographic run time was 8min, and the assay was linear in the concentration range of 1-1000nM. The within- and between day precisions and accuracy were in the range of 2.58-8.71 and 90-105%, respectively. The assay was applied to determine plasma drug concentration in a mouse pharmacokinetic study. It was found that intraperitoneal dosing of 3mg/kg resulted in high systemic exposure and achieved C

Indexed as

Administration, IntravenousAdministration, OralAnimalsBiological AvailabilityChromatography, LiquidFemaleIndolesInjections, IntraperitonealMiceMice, Inbred ICRTandem Mass SpectrometryIndolesverticillinsEpipolythiodioxopiperazine alkaloidsLiquid chromatography–mass spectrometryMousePharmacokineticsPlasmaVerticillin A

Identifiers

PMID28284083
PMCPMC5399420
OpenAlexW2592025407

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.