Abstract

A Ti4+/Zr4+ ion immobilized sorbent was developed by starting from monodisperse-porous titania microbeads, for the isolation of nucleosides via immobilized metal affinity chromatography (IMAC). For the synthesis of IMAC sorbent, the monodisperse-porous titania microbeads were coated with a polydopamine (PDA) layer. PDA coated titania microbeads were then interacted with TiCl4 or ZrOCl2 solution for the immobilization of Ti4+ or Zr4+ ions onto the PDA layer. Five nucleosides (adenosine, uridine, cytidine, thymidine and guanosine) were individually adsorbed onto Ti4+ or Zr4+ immobilized titania microbeads in aqueous buffer in a pH range of 4–9. The desorption of nucleosides was performed in an aqueous formic acid solution. The nucleoside isolation performance of Ti4+ immobilized sorbent was also compared with Zr4+ immobilized sorbent, PDA coated titania and bare titania microbeads. The highest equilibrium adsorptions and the highest desorption yields were obtained with Ti4+ immobilized sorbent for all nucleosides. It was demonstrated that pH 7 was found as the most appropriate for the adsorption of all nucleosides onto Ti4+ immobilized sorbent, which was also close to the physiological pH of urine. The highest equilibrium adsorption was observed with adenosine as 12.67 mg adenosine/g Ti4+ immobilized sorbent. Almost quantitative desorption yields were achieved with all nucleosides adsorbed in a wide range of pH onto Ti4+ immobilized sorbent. With respect to the similar sorbents developed previously, we believe that the proposed sorbent is a promising candidate for being a stationary phase particularly for the construction of micro-column based IMAC systems used in the continuous isolation of nucleosides.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.