Evidence map›Paper›PMID 29795658›Full record

ArticlePloS one2018

A stable isotope dilution tandem mass spectrometry method of major kavalactones and its applications.

Yi Wang, Shainnel O Eans, Heather M Stacy, Sreekanth C Narayanapillai, Abhisheak Sharma, Naomi Fujioka, Linda Haddad, Jay McLaughlin, Bonnie A Avery, Chengguo Xing

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Chemical standardization of kava (Pharmaceutical biology · 2026
    Article
  2. Kava (Nutrients · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Natural Products Inhibition of Cytochrome P450 2B6 Activity and Methadone Metabolism.Drug metabolism and disposition: the biological fate of chemicals · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. 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

10 authors.

Yi WangDepartment of Medicinal Chemistry, University of Florida, Gainesville, Florida, United States of America.
Shainnel O EansDepartment of Pharmacodynamics, University of Florida, Gainesville, Florida, United States of America.
Heather M StacyDepartment of Pharmacodynamics, University of Florida, Gainesville, Florida, United States of America.
Sreekanth C NarayanapillaiDepartment of Medicinal Chemistry, University of Florida, Gainesville, Florida, United States of America.
Abhisheak SharmaDepartment of Pharmaceutics, University of Florida, Gainesville, Florida, United States of America.
Naomi FujiokaMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States of America.
Linda HaddadDepartment of Family Community and Health System Sciences, University of Florida, Gainesville, Florida, United States of America.
Jay McLaughlinDepartment of Pharmacodynamics, University of Florida, Gainesville, Florida, United States of America.
Bonnie A AveryDepartment of Pharmaceutics, University of Florida, Gainesville, Florida, United States of America.
Chengguo XingDepartment of Medicinal Chemistry, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0002-4266-6236

Funding

Dihydromethysticin (DHM) for Lung Cancer ChemopreventionR01CA193278 · NCI · UNIVERSITY OF MINNESOTA · PI XING, CHENGGUO · 2015 to 2019
$1.7M
NCI NIH HHS R01 CA193278
6 · The paper itself

Abstract

Kava is regaining its popularity with detailed characterizations warranted. We developed an ultraperformance liquid chromatography high-resolution tandem mass spectrometry (UPLC-MS/MS) method for major kavalactones (kavain, dihydrokavain, methysticin, dihydromethysticin and desmethoxyyangonin) with excellent selectivity and specificity. The method has been validated for different matrices following the Food and Drug Administration guidance of analytical procedures and methods validation. The scope of this method has been demonstrated by quantifying these kavalactones in two kava products, characterizing their tissue distribution and pharmacokinetics in mice, and detecting their presence in human urines and plasmas upon kava intake. As expected, the abundances of these kavalactones differed significantly in kava products. All of them exhibited a large volume of distribution with extensive tissue affinity and adequate mean residence time (MRT) in mice. This method also successfully quantified these kavalactones in human body fluids upon kava consumption at the recommended human dose. This UPLC-MS/MS method therefore can be used to characterize kava products and its pharmacokinetics in animals and in humans.

Indexed as

Radioisotope Dilution TechniqueAnimalsHumansKavaLactonesMaleMiceMice, Inbred C57BLPyronesTandem Mass SpectrometryTissue DistributionUrinalysis7,8-dihydromethysticindesmethoxyyangonindihydrokavainkavainLactonesPyrones

Identifiers

PMID29795658
PMCPMC5993114

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LicenceCC BY
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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.