Evidence map›Paper›PMID 34365292›Full record

ArticleJournal of chromatography. B, Analytical technologies in the biomedical and life sciences2021

Developing a SWATH capillary LC-MS/MS method for simultaneous therapeutic drug monitoring and untargeted metabolomics analysis of neonatal plasma.

Jingcheng Xiao, Jian Shi, Ruiting Li, Lucy Her, Xinwen Wang, Jiapeng Li, Matthew J Sorensen, Varsha Bhatt-Mehta, Hao-Jie Zhu

Open access · greenAbstract read
In one paragraph

Article in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  3. Review
  4. 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

9 authors at 2 institutions in 1 country.

Jingcheng XiaoDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109, United States.
Jian ShiDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI 48109, United States.
Ruiting LiDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109, United States.
Lucy HerDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109, United States.
Xinwen WangDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, OH 44272, United States.
Jiapeng LiDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI 48109, United States.
Matthew J SorensenDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.
Varsha Bhatt-MehtaDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI 48109, United States; Department of Pediatrics and Communicable Diseases, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, United States.
Hao-Jie ZhuDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI 48109, United States. Electronic address: hjzhu@med.umich.edu.
University of Michigan–Ann Arbor · USNortheast Ohio Medical University · US

Funding

Carboxylesterase 1 Genetic Variation and Methylphenidate in ADHDR01HD093612 · NICHD · UNIVERSITY OF FLORIDA · PI MARKOWITZ, JOHN S, ZHU, HAOJIE · 2018 to 2022
$3.0M
Genetic determinants of ACEI prodrug activationR01HL126969 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHU, HAOJIE · 2016 to 2020
$1.9M
NHLBI NIH HHS R01 HL126969NICHD NIH HHS R01 HD093612
6 · The paper itself

Abstract

Most medications prescribed to neonatal patients are off-label uses. The pharmacokinetics and pharmacodynamics of drugs differ significantly between neonates and adults. Therefore, personalized pharmacotherapy guided by therapeutic drug monitoring (TDM) and drug response biomarkers are particularly beneficial to neonatal patients. Herein, we developed a capillary LC-MS/MS metabolomics method using a SWATH-based data-independent acquisition strategy for simultaneous targeted and untargeted metabolomics analysis of neonatal plasma samples. We applied the method to determine the global plasma metabolomics profiles and quantify the plasma concentrations of five drugs commonly used in neonatal intensive care units, including ampicillin, caffeine, fluconazole, vancomycin, and midazolam and its active metabolite α-hydroxymidazolam, in neonatal patients. The method was successfully validated and found to be suitable for the TDM of the drugs of interest. Moreover, the global metabolomics analysis revealed plasma metabolite features that could differentiate preterm and full-term neonates. This study demonstrated that the SWATH-based capillary LC-MS/MS metabolomics approach could be a powerful tool for simultaneous TDM and the discovery of neonatal plasma metabolite biomarkers.

Indexed as

BiomarkersChromatography, LiquidDrug MonitoringHumansInfant, NewbornMetabolomeMetabolomicsPharmaceutical PreparationsTandem Mass SpectrometryBiomarkersPharmaceutical PreparationsData-independent acquisitionSWATHTherapeutic drug monitoringUntargeted metabolomics

Identifiers

PMID34365292
PMCPMC8403149
OpenAlexW3186230759

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.