Evidence map›Paper›PMID 40768086›Full record

ArticleMikrochimica acta2025

Development of an electrochemical sensor using molecularly imprinted polymers for the specific determination of the antiretroviral drug ritonavir.

Abdullah Al Faysal, Ahmet Cetinkaya, Taner Erdoğan, Sibel A Ozkan, Ayşegül Gölcü

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Article in Mikrochimica acta, 2025. 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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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Abdullah Al FaysalDepartment of Chemistry, Faculty of Sciences and Letters, Istanbul Technical University, Maslak, Istanbul, Turkey.
Ahmet CetinkayaDepartment of Analytical Chemistry, Gülhane Faculty of Pharmacy, University of Health Sciences, Ankara, Turkey.
Taner ErdoğanDepartment of Chemistry and Chemical Processing Technologies, Kocaeli Vocational School, Kocaeli University, Kocaeli, Turkey.
Sibel A OzkanDepartment of Analytical Chemistry, Faculty of Pharmacy, Ankara University, Ankara, Turkey. sibel.ozkan@pharmacy.ankara.edu.tr.
Ayşegül GölcüDepartment of Chemistry, Faculty of Sciences and Letters, Istanbul Technical University, Maslak, Istanbul, Turkey. aysgolcu@itu.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An innovative sensor technology is introduced that employs molecularly imprinted polymers (MIPs) for the electrochemical detection of ritonavir (RTV), a protease inhibitor utilized in HIV therapy. RTV is frequently used in combination with other drugs since it is also a significant inhibitor of the P450 3A4 isoenzyme. Therefore, accurate detection of RTV in complex mixtures and intricate biological matrices is necessary to evaluate the therapeutic efficacy of RTV. A polymeric layer was formed on the surface of the glassy carbon electrode (GCE) using RTV as the template molecule, methacrylic acid (MAA) as the functional monomer, and aniline in a phosphate buffer at pH 7. The morphological and electrochemical characteristics of the RTV/ANI-co-MAA@MIP-GCE sensor were assessed through scanning electron microscopy, Fourier transform infrared spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. The sensor exhibited a linear detection range for RTV utilizing a redox probe (5.0 mM [Fe(CN)

Indexed as

Anti-Retroviral AgentsElectrochemical TechniquesMolecularly Imprinted PolymersRitonavirElectrodesHumansLimit of DetectionMethacrylatesMolecular ImprintingAnti-Retroviral AgentsMethacrylatesmethacrylic acidMolecularly Imprinted PolymersRitonavirComputational designElectrochemical sensorElectropolymerizationModified glassy carbon electrodeMolecularly imprinted polymersRitonavir

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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.