Mori Tomoko, Takahashi Teruki, Shiyama Takaaki, Tanaka Akito, Hira Natsuki, Tanaka Nobuo, Hosoya Ken
Graduate School of Science and Technology, Department of Biomolecular Engineering, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku,Japan.
Bioorg Med Chem. 2006 Aug 15;14(16):5549-54. doi: 10.1016/j.bmc.2006.04.028. Epub 2006 May 8.
An easy preparation method of monolithic type hydrophilic solid phase was discussed. Newly invented functional monomer with a hydrophilic cross-linking agent was co-polymerized to realize well-controlled monolithic co-continuous structure by use of diethylene glycol as porogenic solvent. We were able to control the content of the functional monomer up to 40 vol% without loss of monolithic structure. Those prepared were utilized as affinity resins after immobilization of FK506, an immunosuppressive drug as a ligand. It was found that the affinity resins prepared were hydrophilic enough to eliminate non-specific adsorption of proteins, while two of the target proteins of FK506 tested were successfully captured.