The novel route to prepare immobilized macrocyclic compound on 6-OH of chitosan with good solubility and prime study on its applications

Chen Yu*, Li Wei-Ping, Ye Yan-Chun, Guo Yan-Wen, Wang Tian-Wei, Xing Yi-Fan

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

β-cyclodextrin (β-CD) immobilization of a chitosan derivate on C6-OH (CTS-6-CD) with good solubility was prepared through a novel method. During the process the amino group of the chitosan was protected by phthalic anhydride and deprotected in the hydrazine hydrate solution. β-CD was immobilized onto the C6 position of chitosan by a nucleophilic displacement reaction. The prepared derivate can be dissolved in hydrazine hydrate (v:v = 1:1), ethylenediamine/ethanol (v:v = 1:1), 1% aqueous acetic acid, DMSO and DMAc. The application of the 6-OH cyclodextrin-immobilized chitosan derivatives in an electrochemical biosensor was examined in a preliminarily manner.

Original languageEnglish
Pages (from-to)202-212
Number of pages11
JournalMolecular Crystals and Liquid Crystals
Volume604
Issue number1
DOIs
Publication statusPublished - 22 Nov 2014

Keywords

  • Chitosan
  • immobilization
  • nucleophilic displacement reaction
  • solubility
  • β-cyclodextrin

Fingerprint

Dive into the research topics of 'The novel route to prepare immobilized macrocyclic compound on 6-OH of chitosan with good solubility and prime study on its applications'. Together they form a unique fingerprint.

Cite this