Simultaneous determination of macrolides in water samples by solid-phase extraction and capillary electrophoresis.

Autor:	Pavlović DM; 1University of Zagreb Faculty of Chemical Engineering and Technology, Department of Analytical Chemistry, 10000 Zagreb, Croatia., Babić S; 1University of Zagreb Faculty of Chemical Engineering and Technology, Department of Analytical Chemistry, 10000 Zagreb, Croatia., Čizmić M; 1University of Zagreb Faculty of Chemical Engineering and Technology, Department of Analytical Chemistry, 10000 Zagreb, Croatia., Sertić M; 2University of Zagreb Faculty of Pharmacy and Biochemistry, Department of Pharmaceutical Analysis, 10000 Zagreb, Croatia., Pinušić T; 1University of Zagreb Faculty of Chemical Engineering and Technology, Department of Analytical Chemistry, 10000 Zagreb, Croatia.
Jazyk:	angličtina
Zdroj:	Acta pharmaceutica (Zagreb, Croatia) [Acta Pharm] 2023 Dec 26; Vol. 73 (4), pp. 515-535. Date of Electronic Publication: 2023 Dec 26 (Print Publication: 2023).
DOI:	10.2478/acph-2023-0041
Abstrakt:	Solid-phase extraction (SPE) coupled with capillary electrophoresis (CE) for the determination of macrolide antibiotics (azithromycin, clarithromycin, roxithromycin, tylosin) and tiamulin in water samples was described in this article. These compounds were extracted with different types of sorbents ( Oasis HLB, C18, C8, SDB, and Strata-X) and different masses of sorbents (60 mg, 200 mg, and 500 mg) using different organic solvents (methanol, ethanol, and acetonitrile) and different pH values of water samples (pH 7.00, 8.00, and 9.00). It was found that the highest extraction efficiency of the studied compounds was obtained with 200 mg/3 mL C18 cartridges with methanol as eluent at pH 9.00 of the water sample. The developed SPE-CE method for macrolide antibiotics and tiamulin was validated for linearity, precision, repeatability, the limit of detection ( LOD ), the limit of quantification ( LOQ ), and recovery. Good linearity was obtained in the range of 0.3-30 mg L -1 depending on the drug, with correlation coefficients higher than 0.9958 in all cases except clarithromycin (0.9873). Expanded measurement uncertainties were calculated for each pharmaceutical, accounting for 20.31 % (azithromycin), 38.33 % (tiamulin), 28.95 % (clarithromycin), 26.99 % (roxithromycin), and 21.09 % (tiamulin). Uncertainties associated with precision and calibration curves contributed the most to the combined measurement uncertainty. The method was successfully applied to the analysis of production waste-water from the pharmaceutical industry. (© 2023 Dragana Mutavdžić Pavlović et al., published by Sciendo.)
Databáze:	MEDLINE
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