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The initial step in this direction was the synthesis and subsequent analysis of L\u2010NEP\u2010maleimide chiral derivative. A 4\u2010vinylpyridine\/divinylbenzene combination was copolymerized with the resultant chiral maleimide. After heating the polymer materials in a high\u2010alkaline environment to breakdown the connecting imide bonds, they were acidified in an HCl solution to eliminate the incorporated L\u2010NEP species. Fourier transform infrared spectroscopy (FTIR) and a scanning electron microscope were used to examine the imprinted L\u2010NEP\u2010imprinted materials. The manufactured L\u2010NEP\u2010imprinted materials exhibited selectivity characteristics that were over 11 times greater for L\u2010NEP than D\u2010norepinephrine. The highest capacity observed in Langmuir adsorption studies was 170\u2009mg\/g at a pH of 7. 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