Evidence mapPaperPMID 41947975Full record

ArticleAnalytical science advances2026

A Novel Ultra-Performance Liquid Chromatography-Electrospray Ionisation-Tandem Mass Spectrometry Method for Quantification of Imeglimin in Human Plasma: Application to a Bioequivalence Study.

Mina Wadie, Kamal A Badr, Ahmed A Hosny, Liliya Logoyda, Omnia M El Sebai, Mamdouh R Rezk

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Article in Analytical science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mina WadiePharmaceutical Analytical Chemistry Department Faculty of Pharmacy, Cairo University Cairo Egypt.
Kamal A BadrAdvanced Research Centre (ARC) Cairo Egypt.
Ahmed A HosnyResearch and Development (R&D) Department Atco Pharma for Pharmaceutical Industries Cairo Egypt.
Liliya LogoydaPharmaceutical Chemistry Department Pharmaceutical Faculty I. Horbachevsky Ternopil National Medical University Ternopil Ukraine.
Omnia M El SebaiAdvanced Research Centre (ARC) Cairo Egypt.
Mamdouh R RezkPharmaceutical Analytical Chemistry Department Faculty of Pharmacy, Cairo University Cairo Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pharmaceutical market has recently witnessed the advent of a novel tetrahydrotriazene molecule belonging to the new pharmacological class "Glimins", named Imeglimin (IMG). It has been approved in Japan as a safe and highly effective oral diabetic drug for type II diabetic patients. It enhances the function of β-cells in the human pancreas and increases insulin sensitivity. Hence, this work was directed to provide a fast, sensitive and highly reliable bioanalytical method for its quantification in human plasma. What makes this work greatly distinctive is first: adopting an ultra-performance liquid chromatography (UPLC) with protein precipitation as a fast and straightforward sample preparation protocol with the highest extraction recovery. Secondly, utilisation of the stable isotope-labelled molecule, IMG-d6, rather than a structurally similar analogue, to avoid the interference of any co-administered drugs in human plasma. Samples were extracted with acetonitrile and then chromatographically separated using an Acquity UPLC BEH HILIC column of 1.7 µm particle size along with a mobile phase solution composed of 70:30 (v/v) acetonitrile and 10 mM ammonium formate buffer acidified with 0.1% formic acid. Upon adjusting the flow rate to 0.3 mL/min, IMG was eluted at 1.3 min with a total run time of only 2.0 min. Mass quantification was performed in positive electrospray ionisation operated in multiple reaction monitoring mode. IMG was quantified at

Indexed as

bioequivalence studyImegliminpharmacokinetic studyprotein precipitationUPLC‐MS/MS

Identifiers

PMID41947975
PMCPMC13053006

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