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http://dx.doi.org/10.5012/jkcs.2009.53.3.279

Preparation of Affinity Column Based on ZR4+ Ion forPhosphoproteins Isolation  

Lee, Seon-Mi (Department of Chemistry, BK 21 NanoBiosensor Research Team, Hannam University)
Bae, In-Ae (Department of Chemistry, BK 21 NanoBiosensor Research Team, Hannam University)
Park, Jung-Hyen (Department of Chemistry, BK 21 NanoBiosensor Research Team, Hannam University)
Kim, Tae-Dong (Department of Advanced Materials, Hannam University)
Choi, Seong-Ho (Department of Chemistry, BK 21 NanoBiosensor Research Team, Hannam University)
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Abstract
This paper has described about preparation of $Zr^{4+}$ affinity column based on the poly(styrene-co- gly-cidyl methacrylate) prepared by emulsion polymerization of styrene and glycidyl methacrylate in order to isolate phosphopeptide. The $Zr^{4+}$ ions were introduced after the phophonation of an epoxy group on polymeric microspheres. The successful preparation of $Zr^{4+}$-immobilized polymeric microsphere stationary phase was confirmed through Fourier transform infrared spectra, optical microscopy, scanning electron microscopy, X-ray photoelectron spectra and inductively coupled plasma-atomic emission spectrometer. The separation efficiency for $Zr^{4+}$ affinity column prepared by slurry packing was tested to phosphonated casein and dephosphonated casein. The resolution time (min) of the phosphonated casein was higher than that of dephosphated casein for $Zr^{4+}$ affinity polymeric microsphere by liquid chromatography. This $Zr^{4+}$ affinity column can be used for isolation of phosphonated casein from casein using liquid chromatography.
Keywords
$ZR^{4+}$ affinity column; poly(styrene-co-glycidyl methacrylate); polymer microsphere; phosphonated casein; resolution time;
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