| Autor: |
Marzullo L; Department of Chemistry 'U. Schiff', University of Florence, 50019 Sesto Fiorentino, Italy., Gotti R; Department of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy., Orlandini S; Department of Chemistry 'U. Schiff', University of Florence, 50019 Sesto Fiorentino, Italy., Slavíčková P; Zentiva, k.s., 10237 Prague, Czech Republic., Jireš J; Zentiva, k.s., 10237 Prague, Czech Republic.; Department of Analytical Chemistry, Faculty of Chemical Engineering, UCT Prague, 16628 Prague, Czech Republic., Zapadlo M; Zentiva, k.s., 10237 Prague, Czech Republic., Douša M; Zentiva, k.s., 10237 Prague, Czech Republic., Nekvapilová P; Department of Analytical Chemistry, Faculty of Chemical Engineering, UCT Prague, 16628 Prague, Czech Republic., Řezanka P; Department of Analytical Chemistry, Faculty of Chemical Engineering, UCT Prague, 16628 Prague, Czech Republic., Furlanetto S; Department of Chemistry 'U. Schiff', University of Florence, 50019 Sesto Fiorentino, Italy. |
| Abstrakt: |
In 2022, the International Council for Harmonisation released draft guidelines Q2(R2) and Q14, intending to specify the development and validation activities that should be carried out during the lifespan of an analytical technique addressed to assess the quality of medicinal products. In the present study, these recommendations were implemented in Capillary Electrophoresis method development for the quality control of a drug product containing trimecaine, by applying Analytical Quality by Design. According to the Analytical Target Profile, the procedure should be able to simultaneously quantify trimecaine and its four impurities, with specified analytical performances. The selected operative mode was Micellar ElectroKinetic Chromatography employing sodium dodecyl sulfate micelles supplemented with dimethyl-β-cyclodextrin, in a phosphate-borate buffer. The Knowledge Space was investigated through a screening matrix encompassing the composition of the background electrolyte and the instrumental settings. The Critical Method Attributes were identified as analysis time, efficiency, and critical resolution values. Response Surface Methodology and Monte Carlo Simulations allowed the definition of the Method Operable Design Region: 21-26 mM phosphate-borate buffer pH 9.50-9.77; 65.0 mM sodium dodecyl sulfate; 0.25-1.29% v / v n -butanol; 21-26 mM dimethyl-β-cyclodextrin; temperature, 22 °C; voltage, 23-29 kV. The method was validated and applied to ampoules drug products. |
