Evidence map›Paper›PMID 42324282›Full record

ArticleScientific reports2026

Hydrophilicity-switchable deep eutectic solvent-based ultrasound-assisted liquid-phase microextraction for the green and efficient spectrofluorimetric determination of verapamil in human plasma.

Hassan Heidari, Aytak Esmaeilzadeh Razi, Mustafa Bener

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Hassan HeidariDepartment of Chemistry, Azarbaijan Shahid Madani University, Tabriz, Iran. hassan_heidari@ymail.com.
Aytak Esmaeilzadeh RaziDepartment of Chemistry, Azarbaijan Shahid Madani University, Tabriz, Iran.
Mustafa BenerDepartment of Chemistry, Faculty of Science, Istanbul University, 34134, Fatih, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a hydrophilicity-switchable deep eutectic solvent (HS-DES) was prepared by combining nonanoic acid (C9) with tetrabutylammonium bromide (TBAB) and applied as an efficient extraction medium for the ultrasound-assisted liquid-phase microextraction (UALPME) of verapamil from human plasma samples prior to spectrofluorimetric determination. The hydrophilicity-hydrophobicity transition of the HS-DES was controlled by pH adjustment using NaOH or HCl solutions, enabling reversible phase switching and facilitating effective separation of verapamil from the biological matrix. Key experimental parameters influencing the extraction efficiency were systematically investigated, and further optimization was performed using a central composite design coupled with a desirability function approach. The developed HS-DES-based UALPME (HS-DES-UALPME) method provides a tunable, environmentally friendly, and effective strategy for the preconcentration of verapamil from complex biological samples. The method showed wide linear range (200-2000 ng/mL), a good limit of detection (62.16 ng/mL), and extraction recovery (59.55%). To assess the method's sustainability, the AGREE tool was applied, clearly demonstrated the overall greenness of the developed procedure. A comparison of the analytical performance of the method with previously reported methods demonstrated its superiority or, at minimum, its comparability in key analytical parameters.

Indexed as

Deep Eutectic SolventsLiquid Phase MicroextractionVerapamilHumansHydrogen-Ion ConcentrationHydrophobic and Hydrophilic InteractionsLimit of DetectionSolventsSpectrometry, FluorescenceDeep Eutectic SolventsSolventsVerapamilDeep eutectic solventGreen analytical chemistryHydrophilicity-switchablePlasmaSpectrofluorimetryVerapamil

Identifiers

PMID42324282
PMCPMC13562515

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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.