Introduction of an electrochemical point‐of‐care assay for quantitative determination of paracetamol in finger‐prick capillary whole blood samples

Author:

Kujala Johanna1ORCID,Wester Niklas234ORCID,Lohela Terhi J.567ORCID,Kurkela Mika57ORCID,Backman Janne T.57ORCID,Mikladal Björn8ORCID,Laurila Tomi23ORCID,Koskinen Jari2ORCID,Lilius Tuomas O.579ORCID,Kalso Eija A.56ORCID

Affiliation:

1. Department of Emergency Medicine and Services Helsinki University Hospital and University of Helsinki Helsinki Finland

2. Department of Chemistry and Materials Science, School of Chemical Engineering Aalto University Helsinki Finland

3. Department of Electrical Engineering and Automation, School of Electrical Engineering Aalto University Helsinki Finland

4. Fepod Oy Ltd, c/o Terkko Health Hub Helsinki Finland

5. Department of Clinical Pharmacology, Faculty of Medicine University of Helsinki and Helsinki University Hospital Helsinki Finland

6. Department of Anaesthesiology, Intensive Care and Pain Medicine Helsinki University Hospital and University of Helsinki Helsinki Finland

7. Individualized Drug Therapy Research Program, Faculty of Medicine University of Helsinki Helsinki Finland

8. Canatu Oy Helsinki Finland

9. Department of Emergency Medicine and Services, Finnish Poison Information Center Helsinki University Hospital and University of Helsinki Helsinki Finland

Abstract

AimsMeasuring venous plasma paracetamol concentrations is time‐ and resource‐consuming. We aimed to validate a novel electrochemical point‐of‐care (POC) assay for rapid paracetamol concentration determinations.MethodsTwelve healthy volunteers received 1 g oral paracetamol, and its concentrations were analysed 10 times over 12 h for capillary whole blood (POC), venous plasma (high‐performance liquid chromatography tandem mass spectrometry (HPLC‐MS/MS)), and dried capillary blood (HPLC‐MS/MS).ResultsAt concentrations >30 μM, POC showed upward biases of 20% (95% limits of agreement [LOA] −22 to 62) and 7% (95% LOA −23 to 38) compared with venous plasma and capillary blood HPLC‐MS/MS, respectively. There were no significant differences between mean concentrations for the paracetamol elimination phase.ConclusionsUpward biases in POC compared with venous plasma HPLC‐MS/MS were likely due to higher paracetamol concentrations in capillary blood than in venous plasma and to faulty individual sensors. The novel POC method is a promising tool for paracetamol concentration analysis.

Funder

Business Finland

Svenska Kulturfonden

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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