Robust open tubular layer of S-ketoprofen imprinted polymer for chiral LC separation

This study is about the preparation of an open tubular capillary column of molecularly imprinted polymer (MIP) and its application to chiral separation by mu LC. A noncovalent in-situ molecular imprinting polymerization protocol was used to synthesize the S-ketoprofen Mill. A special procedure was employed to secure formation of an open tubular and rigid MIP layer in a silica capillary of 100 pin id. The capillary was filled with the reaction mixture, sealed, and placed in a water bath at 50 degrees C for 3 h. Then it was flushed with a 0.5 MPa nitrogen flow for 5 min, and was again placed in the water bath for 2 h to complete Mill formation. Methacrylic acid (MAA) has been known to be an inefficient functional monomer in preparation of MIP of an acid molecule. However, MAA was used with ethylene glycol dimethacrylate in preparation of the S-ketoprofen Mill in this study. The open tubular structure and the mu LC mode of separation enabled free optimization without any restriction, thus a very good resolution (R = 4.7) of ketoprofen enantiomers was achieved when a mobile phase composed of 30% acetonitrile and 70% acetate buffer at pH 4.5 was used with 5 mbar inlet pressure. This may be partially attributed to the open tubular structure of our MIP, enabling low column back-pressure and free optimization of eluent composition, as well as to the small capillary dimensions. Our MIP capillary column also showed some versatility in chiral separation, thus a good chiral separation was observed for naproxen, ibuprofen, and fenoprofen enantiomers.