Polymers (May 2022)

Studies on Intermolecular Interaction of <i>N</i>-Glycidyltrimethyl Ammonium Chloride Modified Chitosan/<i>N</i>,<i>N</i>-Dimethyl-<i>N</i>-dodecyl-<i>N</i>-(2,3-epoxy propyl) Ammonium Chloride and Curcumin Delivery

  • Cangheng Zhang,
  • Yan Li,
  • Shu Xing,
  • Xiaodeng Yang,
  • Jinrong Zhao,
  • Qiaoyan Dong

DOI
https://doi.org/10.3390/polym14101936
Journal volume & issue
Vol. 14, no. 10
p. 1936

Abstract

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Chitosan has potential applications in many fields, due to its biocompatibility, biodegradability and reproducibility. However, the insolubility in water restricts its wide application. In order to expand the application of chitosan in the delivery of oil-soluble drugs and improve the efficacy of oil-soluble drugs, N-Glycidyltrimethyl ammonium chloride-modified chitosan (GTA-m-CS) and N,N-Dimethyl-N-dodecyl-N-(1,2-epoxy propyl) ammonium chloride (DDEAC), a kind of reactive surfactant, were synthesized and characterized by FTIR, NMR and XRD methods. The interactions between GTA-m-CS and DDEAC was studied by surface tension, viscosity, conductivity and fluorescence methods. The parameters, including equilibrium surface tension, critical micelle concentrations of DDEAC with different GTA-m-CS concentration, critical aggregation concentration of DDEAC, the amount of DDEAC adsorbed on GTA-m-CS, pc20 and πcmc were obtained from the surface tension curves. The influence of temperature on the above parameters were evaluated. The degree of counterion binding to micelle and the thermodynamic parameters of the system were calculated from the conductivity curves. According to the change of conductivity with temperature, the thermodynamic parameters of micellar formation were calculated. The aggregation number of DDEAC molecules in GTA-m-CS/DDEAC aggregates were calculated from steady-state fluorescence data. Based on the experimental results, the interaction models between GTA-m-CS and DDEAC were proposed. The GTA-m-CS/DDEAC aggregates could be used as curcumin carries, and achieved sustained release.

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