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Pitfalls and success of experimental design in the development of a mixed MEKC method for the analysis of budesonide and its impurities
Author(s) -
Furlanetto Sandra,
Orlandini Serena,
Giannini Iacopo,
Beretta Giangiacomo,
Pinzauti Sergio
Publication year - 2009
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.200800626
Subject(s) - resolution (logic) , chemistry , budesonide , sodium cholate , chromatography , boron , micelle , analytical chemistry (journal) , computer science , organic chemistry , medicine , artificial intelligence , aqueous solution , inhalation , anatomy
A mixed MEKC method for the analysis of budesonide and its related substances is presented. The micelles were formed from sodium cholate (CHOL) and 3‐( N , N ‐dimethylmyristylammonio)propanesulfonate (MAPS). A multivariate optimisation was carried out with the aim of obtaining a baseline separation of all compounds. The influence of voltage, borate concentration, cholate concentration, MAPS concentration and pH was evaluated on the responses, corresponding to critical resolution values. Problems with the investigated experimental design were encountered due to the complexity of the separation process. As a consequence, a first design was not sufficient to reach the optimal conditions, but was needed in order to obtain the necessary information to successfully plan a second in‐depth study by means of response surface methodology. The optimal conditions were as follows: capillary total and effective lengths of 48.5 and 40.0 cm, respectively, with 50 μm id; 70 mM borate buffer (pH 8.8) containing 65 mM CHOL and 10 mM MAPS; temperature 20°C and voltage 16 kV. Separation of all the compounds, including R ‐ and S ‐epimers of budesonide, was obtained in a reasonable time. Validation of the method was performed for both drug substances and drug product.