The potential of three different adsorbents in solid‐phase extraction of antihistaminic and antimigraine drugs from water samples using ultra‐high‐performance liquid chromatography‐ultraviolet analysis

Author:

Jebali Sami1,Labidi Aymen2,Sghaier Rafika Ben34,Latrous Latifa45ORCID,Megriche Adel4

Affiliation:

1. Institut National de Recherche et d'Analyse Physico‐ chimique Laboratoire Matériaux Traitement et Analyse Ariana Tunisia

2. Laboratoire National de contrôle des médicaments Tunis Tunisia

3. Laboratory of Composite Materials and Clay Minerals National Center of Researches in Material Sciences Soliman Tunisia

4. Université de Tunis El Manar Faculté des Sciences de Tunis Laboratoire de chimie minérale appliquée, Campus universitaire Département de Chimie Tunis Tunisia

5. Institut Préparatoire aux Etudes d'Ingénieurs d'El Manar Département de Chimie Tunis Tunisia

Abstract

AbstractIn this study, eight pharmaceuticals belonging to two classes, antihistaminic and antimigraine, were considered. Ultra‐performance liquid chromatography‐diode array detection was set up and gradient elution was used. The mobile phase was composed of acetonitrile and trifluoroacetic acid solution. Chromatographic separation was carried out with a run time of 9 min. The preconcentration of eight studied solutes was realized by micro solid‐phase extraction. Multiwalled carbon nanotubes, cetyltrimethylammonium bromide‐titanium dioxide nanotubes, and C‐18 bonded silica solid‐phase extraction (SPE) sorbents were evaluated and compared concerning recoveries. The results of the optimization of factors affecting the extraction efficiency including sample volume, the elution solvent type, and its volume are reported. For validation of the analytical procedure, specificity, linearity, precision, accuracy, limit of detection, and limit of quantification were evaluated. The developed method was successfully applied to the analysis of wastewater treatment samples. The extraction recoveries of pharmaceutical substances were above 81.23% for the three SPE sorbents. The extraction method was selective and the detection and quantification limits were between 0.004–0.02 and 0.01–0.06 μg/L, respectively. All the results indicated the potential application of the three studied SPE sorbents for the extraction of selected pharmaceuticals from wastewater.

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

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