A mixed‐bed, multi‐derivatization approach using polymeric reagents for derivatizations of amines in high performance liquid chromatographic detection

Immobilized, polymeric reagents containing covalently attached tagging groups have been synthesized and reacted individually, off‐line or on‐line, pre‐column in high performance liquid chromatographic (HPLC) detection. These reagents have also been combined into a single, mixed‐bed reactor, useful for simultaneously preparing several derivatives from a single analyte, all at the same time. Each derivative possesses different chromatographic and detection properties, dependent on the nature of the original polymeric reagent containing the immobilized, tagging species. These particular reagents were designed to impart Ultraviolet/fluorescence, Ultraviolet/electrochemistry (oxidative/reductive or oxidative‐ hv ‐electrochemistry) to the final derivatives. Variations in the amounts/ratios of polymeric reagents contained in a single mixed‐bed reactor will lead to varying ratios of the final derivatives. These can be predicted knowing the approximate reactivity of each polymeric reagent, percent derivatizations, and overall rates for each reagent towards a given substrate. In this first example of mixed‐bed, polymeric reagents for improved derivatization approaches in chromatography, emphasis has been placed on simple amines or amine‐like analytes. Multiple derivatives can be effectively used to improve the identification of an unknown analyte in a complex sample matrix, as well as to improve the detectability of that analyte. As one real world application, amphetamine in human urine was quantitated via on‐line derivatizations‐with a mixed‐bed reactor. With the least sampling work‐up, the resulting sample solutions were directly injected into the on‐line derivatization HPLC system for quantitation. The method was validated by single blind spiking experiments. The precision and accuracy were acceptable.