Evidence map›Paper›PMID 40792418›Full record

ArticleBiomedical chromatography : BMC2025

Development and Validation of a LC-MS/MS Method for Ripretinib and Its Metabolite: Example of a Journey From Laboratory Bench to Routine Application With a Greenness Assessment.

Cedric Rakotovao, Ahmad Sharanek, Audrey Burban, Paul Gueroue, Stéphane Bouchet, Guillaume Bouguéon, Dominique Ducint, Mathieu Molimard, Antoine Italiano, Sarah Djabarouti and 1 more

Abstract read
In one paragraph

Article in Biomedical chromatography : BMC, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Cedric RakotovaoDepartment of Pharmacy, CHU Bordeaux, Pessac, France.
Ahmad SharanekBRIC, UMR1312, Univ. Bordeaux, INSERM, Bordeaux, France.
Audrey BurbanIBGC, UMR5095, Univ. Bordeaux, CNRS, Bordeaux, France.
Paul GueroueDepartment of Medical Pharmacology, CHU Bordeaux, Bordeaux, France.
Stéphane BouchetDepartment of Medical Pharmacology, CHU Bordeaux, Bordeaux, France.
Guillaume BouguéonDepartment of Pharmacy, CHU Bordeaux, Pessac, France.
Dominique DucintDepartment of Medical Pharmacology, CHU Bordeaux, Bordeaux, France.
Mathieu MolimardDepartment of Medical Pharmacology, CHU Bordeaux, Bordeaux, France.
Antoine ItalianoBRIC, UMR1312, Univ. Bordeaux, INSERM, Bordeaux, France.
Sarah DjabaroutiDepartment of Pharmacy, CHU Bordeaux, Pessac, France.
Joris GuyonBRIC, UMR1312, Univ. Bordeaux, INSERM, Bordeaux, France.ORCID https://orcid.org/0000-0001-6692-2890

Funding

Association pour la Recherche sur les Tumeurs Cérébrales 283008Bordeaux Institute of Oncology (BRIC)Bordeaux University HospitalFondation de France
6 · The paper itself

Abstract

Therapeutic drug monitoring of protein kinase inhibitors is widely practiced worldwide. Based on the example of ripretinib dosage requested by a clinician, we detailed the process of method development, using a literature-based approach while ensuring the sustainability of the method to be as environmentally friendly as possible. Therefore, a UPLC-MS/MS method for ripretinib and its active metabolite was optimized and validated using the corresponding stable isotopic internal standards in human plasma. The procedure employed a mobile phase mixture of water with 1% acetic acid and 0.1% formic acid, and acetonitrile. Positive electrospray ionization was performed, coupling with multiple reaction monitoring of m/z 510.4 → 417.4 and 510.4 → 389.4 for ripretinib, and 496.3 → 403.3 and 496.3 → 375.3 for N-desmethyl-ripretinib. The method was successfully validated according to the current version of the ICH Guideline provided by the EMA. The greenness assessment score of this procedure was better than previously published approaches using the AGREE metric. The validated UPLC-MS/MS method successfully monitored ripretinib and its metabolite concentrations in clinical and preclinical models.

Indexed as

Tandem Mass SpectrometryAnimalsChromatography, High Pressure LiquidChromatography, LiquidHumansLimit of DetectionLinear ModelsLiquid Chromatography-Mass SpectrometryReproducibility of ResultsLC‐MS/MSN‐desmethyl‐ripretinibpharmacokineticripretinibTDM

Identifiers

PMID40792418
PMCPMC12340740

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.