Application of capillary zone electrophoresis to determine second-generation H1 antihistaminic drugs, loratadine and rupatadine

Authors

  • Cintia Maria Alves Mothé University of São Paulo, Faculty of Pharmaceutical Sciences, Department of Pharmacy, São Paulo, SP, Brazil
  • Aline de Souza University of São Paulo, Faculty of Pharmaceutical Sciences, Department of Pharmacy, São Paulo, SP, Brazil https://orcid.org/0000-0003-4307-6497
  • Anil Kumar Singh University of São Paulo, Faculty of Pharmaceutical Sciences, Department of Pharmacy, São Paulo, SP, Brazil
  • Nádia Araci Bou-Chacra University of São Paulo, Faculty of Pharmaceutical Sciences, Department of Pharmacy, São Paulo, SP, Brazil
  • María Segunda Aurora-Prado University of São Paulo, Faculty of Pharmaceutical Sciences, Department of Pharmacy, São Paulo, SP, Brazil

DOI:

https://doi.org/10.1590/s2175-97902022e20767

Keywords:

Antihistamines, Quality control, Capillary electrophoresis, Analytical method development

Abstract

The second generation of H1 antihistamines from the piperidine group are often used for treating allergic diseases due to their action on histaminic receptors, the primary mediator of allergy. Moreover, the antihistamines have anti-inflammatory action, mediated through platelet-activating factor blocking activity. A simple and rapid capillary zone electrophoresis method was developed and validated for the determination of loratadine (LOR) and rupatadine (RUP) in tablets. The analyses were carried out using a fused silica capillary of 50.2 cm (40 cm effective length), 75 µm i.d. The background electrolyte was composed of boric acid 35 mmol/L, pH 2.5. Voltage of 20 kV, hydrodynamic injection of 3447.3 Pa for 3s, temperature at 25 ºC, and UV detection at 205 nm were applied. Electrophoretic separation was achieved at 1.8 and 2.8 min for RUP and LOR, respectively. The method was linear for both drugs in a range of 50.0 to 400.0 μg/mL (r>0.99). The limits of detection and quantification were 46.37 and 140.52 μg/mL, for LOR and 29.60 and 89.69 μg/mL for RUP respectively. The precision was less than 5.0 % for both drugs. The average recovery was approximately 100 %. The proposed novel method can significantly contribute to the rapid detection of counterfeit products and in quality control of drug products containing antihistamines.

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Published

2023-02-07

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Original Article

How to Cite

Application of capillary zone electrophoresis to determine second-generation H1 antihistaminic drugs, loratadine and rupatadine. (2023). Brazilian Journal of Pharmaceutical Sciences, 58. https://doi.org/10.1590/s2175-97902022e20767