Evidence map›Paper›PMID 41636946›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2026

Stability of Colistin Active Forms in Biological Matrices: Effect of Temperature and Time.

Vendula Kubíčková, Jitka Rychlíčková, Karel Urbánek, Zuzana Rácová

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Article in European journal of drug metabolism and pharmacokinetics, 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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1citing papers in PubMed
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1 · What the graph read from it

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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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Vendula KubíčkováDepartment of Pharmacology, Faculty of Medicine and Dentistry, Palacký University Olomouc and University Hospital Olomouc, Hněvotínská 3, 77900, Olomouc, Czech Republic. kubickova.vendula@gmail.com.ORCID http://orcid.org/0000-0002-9305-8732
Jitka RychlíčkováInternational Clinical Research Center, St. Anne's University Hospital Brno, Pekařská 664/53, 65691, Brno, Czech Republic.
Karel UrbánekDepartment of Pharmacology, Faculty of Medicine and Dentistry, Palacký University Olomouc and University Hospital Olomouc, Hněvotínská 3, 77900, Olomouc, Czech Republic.
Zuzana RácováDepartment of Pharmacology, Faculty of Medicine and Dentistry, Palacký University Olomouc and University Hospital Olomouc, Hněvotínská 3, 77900, Olomouc, Czech Republic.

Funding

MEYS, LRI CZECRIN LM2023049
6 · The paper itself

Abstract

backgroundThis study investigated the effects of temperature and concentration on the short-term stability of colistin and colistin methanesulphonate in three biological matrices; whole blood, plasma and serum.

methodsHuman whole blood, plasma or serum containing colistin (2; 10; 20 mg/L) or colistin methanesulphonate (2; 10; 20 mg/L) was stored at room temperatrure or at 37 °C for a predetermined time interval. The concentrations of colistin in colistin spiked samples, and formed colistin in colistin methanesulphonate spiked samples, were analysed by LC-MS method.

resultsFindings indicate that colistin A and B were stable at the room temperature, but degradation accelerated at 37 °C, particularly at lower concentrations. The conversion of CMS to colistin was also temperature-dependent, where the concersion was significantly accelerated at elevated temperatures. Freeze-thaw stability were tested, COL A as well as COL B were stable for at least three freeze-thaw cycles.

conclusionThese results underscore the importance of rapid sample processing to ensure reliable therapeutic drug monitoring and emphasize the importance of considering temperature and concentration factors in clinical practice to optimise dosing and minimise toxicity. Further research is required to investigate the full range of factors affecting the stability of colistin and colistin methanesulphonate in biological matrices.

Indexed as

Anti-Bacterial AgentsColistinChromatography, LiquidDrug MonitoringDrug StabilityFreezingHumansTemperatureTime FactorsAnti-Bacterial AgentsColistin

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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.