Add time:08/06/2019         Source:sciencedirect.com

In this work, polymerizable (4-vinylbenzoyl)-l-tryptophan (VBLT) was synthesized and characterized utilizing, elemental analysis, mass spectra, FTIR, 1H and 13C NMR. VBLT was then copolymerized with styrene and divinylbenzene cross-linker using potassium persulfate free radical initiator. The template l-Trp molecules were then leached out from the cross-linked network leaving selective recognition cavities, which are able to selectively rebind with l-Trp than d-Trp. The obtained molecularly imprinted LT-CPS resin was examined using various instrumental techniques such as SEM and FTIR to be then employed in a series of adsorption experiments to evaluate the essential parameters for efficient selective extraction of l-Trp. The kinetics of adsorption displayed the best fit with pseudo-second-order kinetic model, suggesting chemical sorption as the rate determining step. Additionally, the most effective interpretation of the adsorption isotherm data was acquired by Langmuir isotherm, and the maximum adsorption capacities were 155 ± 2 and 82 ± 1 mg/g for l- and d-Trp, respectively. Moreover, chiral resolution of l, d-Trp racemic mixture was performed using column of LT-CPS.

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