Evidence map›Paper›PMID 36559146›Full record

ArticlePharmaceutics2022

Identification of the Major Degradation Pathways of Selumetinib.

Tahar Sif Eddine Bouchema, Maxime Annereau, Victoire Vieillard, Raphael Boquet, Gisele Abreu Coelho, Florence Castelli, Audrey Solgadi, Muriel Paul, Najet Yagoubi, Philippe-Henri Secretan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. 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
0.3field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

11 authors at 5 institutions in 1 country.

Tahar Sif Eddine BouchemaMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.
Maxime AnnereauMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.ORCID 0000-0001-9594-2516
Victoire VieillardDepartment of Pharmacy, Henri Mondor Hospital, AP-HP, 94000 Créteil, France.
Raphael BoquetDepartment of Pharmacy, Henri Mondor Hospital, AP-HP, 94000 Créteil, France.
Gisele Abreu CoelhoMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.ORCID 0000-0003-1340-6061
Florence CastelliDépartement Médicaments et Technologies pour la Santé (DMTS), MetaboHUB, CEA, INRAE, Université Paris-Saclay, 91191 Gif-sur-Yvette, France.ORCID 0000-0002-6886-8549
Audrey SolgadiIngénierie et Plateformes au Service de l'Innovation Thérapeutique, Inserm, CNRS, Université Paris-Saclay, 92296 Châtenay-Malabry, France.
Muriel PaulDepartment of Pharmacy, Henri Mondor Hospital, AP-HP, 94000 Créteil, France.
Najet YagoubiMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.
Philippe-Henri SecretanMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.ORCID 0000-0002-5838-3695
Bernard DoMatériaux et Santé, Université Paris-Saclay, 91400 Orsay, France.
Université Paris-Saclay · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selumetinib is administered orally in capsule form and is indicated for the treatment of neurofibromatosis. To facilitate dosage adjustments, liquid preparations, such as solutions or suspensions, are to be developed. This led, first, to determine the stability profile of soluble or dispersed selumetinib and, secondly, to look for ways to stabilize the active substance. The degradation kinetics of selumetinib as a function of stress conditions were determined and compared. The degradation products were detected and identified by LC-HRMS

Indexed as

degradation pathwaysESI-MS fragmentation pathwaysintrinsic stabilityoxidationphotooxidationpre-formulation studiesprotein kinase inhibitor

Identifiers

PMID36559146
PMCPMC9787286
OpenAlexW4311046025

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.