Van Overbeke A, Baeyens W, Van den Bossche W, Dewaele C
Laboratory of Drug Analysis, Faculty of Pharmaceutical Sciences, University of Ghent, Belgium.
J Pharm Biomed Anal. 1994 Jul;12(7):901-9. doi: 10.1016/0731-7085(94)e0019-w.
The enantiomers of eight 2-arylpropionic acids, a group of chiral non steroidal antiinflammatory drugs, were resolved as their benzylamide derivatives on a high-performance liquid chromatographic chiral stationary phase consisting of a covalently bound tris (4-methylbenzoate) cellulose layer on silica gel. The column was used under reversed-phase conditions using methanol as the main mobile phase component, with a perchlorate buffer pH 2.0. A compromise for derivatization with a water soluble carbodiimide and 1-hydroxybenzotriazole of a group of eight analytes was obtained. The derivatives were identified by IR- and MS-spectroscopy.