Evidence map›Paper›PMID 41721126›Full record

ReviewMikrochimica acta2026

Research progress in electrochemical determination of Janus kinase inhibitors and proposals for amplifying clinical applicability.

Peter Mikus, Michal Hanko, Zuzana Zelinkova, Jan Labuda

Abstract readReview
In one paragraph

Review in Mikrochimica acta, 2026. 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
–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

0 citing papers in PubMed.

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

4 authors.

Peter MikusDepartment of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, Odbojarov Street 10, Bratislava 3, Bratislava, 832 32, Slovakia. mikus@fpharm.uniba.sk.ORCID 0000-0001-5755-9970
Michal HankoDepartment of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, Odbojarov Street 10, Bratislava 3, Bratislava, 832 32, Slovakia.ORCID 0000-0003-2652-7727
Zuzana ZelinkovaDepartment of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, Odbojarov Street 10, Bratislava 3, Bratislava, 832 32, Slovakia.
Jan LabudaDepartment of Pharmaceutical Analysis and Nuclear Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, Odbojarov Street 10, Bratislava 3, Bratislava, 832 32, Slovakia. jan.labuda@stuba.sk.ORCID 0000-0001-6953-6522

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Janus kinase inhibitors (JAKis) represent a class of drugs that treat inflammatory and autoimmune diseases by blocking Janus kinase (JAK) enzymes. Monitoring of precise drug concentration ensures therapeutic effect while minimizing the risk of toxicity. In parallel to conventional methods based on high performance liquid chromatography, liquid chromatography − mass spectrometric or spectrometric methods, sensitive electrochemical methods for the detection of JAKis have been developed in very recent years. The procedures utilize conventional bare glassy carbon electrode or boron-doped diamond electrode and, particularly, chemically modified electrodes incorporating nanomaterials and their composites as powerful catalysts as well as imprinted polymers. The linear concentration ranges and limits of detection achieve very low 10− 9 M to 10− 12 M (µg to ng/mL) values, matching clinically relevant drug levels and are applied to analysis of biological matrices and pharmaceutical products. In this study, the concentration ranges obtained for individual JAKis are presented and compared with those of conventional methods. The manuscript covers the years 2022 to 2025 highlighting the JAKis electrochemical detection as a new topic. The paper aims to address both current trends and future potential in the development of novel sensors and procedures for the JAK inhibitors detection directed to a real-time point-of-care analysis enabling personalized therapeutic drug monitoring. Advantages and disadvantages of electrochemical approaches for the JAKis assay in clinical settings are critically evaluated. To facilitate the development of more reliable, robust and clinically applicable electrochemical methods, a few recommendations that future studies should follow are proposed.

Indexed as

Electrochemical TechniquesJanus Kinase InhibitorsElectrodesHumansLimit of DetectionJanus Kinase InhibitorsBiological fluid analysisElectrochemical sensors Glassy carbon electrodes; Nanomaterial modified electrodes; Imprinted polymersJanus kinase inhibitorsPharmaceutical dosage forms analysis

Identifiers

PMID41721126
PMCPMC12923409

What Socratic holds

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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 Socratic graph.