Synthesis and characterization of enzymatically cross-linked feruloyl amylopectin for curcumin encapsulation

Int J Biol Macromol. 2016 Apr:85:126-32. doi: 10.1016/j.ijbiomac.2015.12.073. Epub 2015 Dec 28.

Abstract

Feruloyl amylopectin (FAP) was synthesized by the N,N'-carbonyldiimidazole (CDI) activation method, and the enzymatically cross-linked feruloyl amylopectin (CL-FAP) was prepared via catalysis of horseradish peroxidase (HRP) with the presence of hydrogen peroxide (H2O2). RP-HPLC-DAD/ESI-TOF-MS measured ferulic acid and its derivatives in FAP and CL-FAP. FAP was primarily composed of two ferulate monomers, while CL-FAP was composed of two ferulate monomers and two ferulate dehydrodimers. The ester formation in the feruloyl group was confirmed by the presence of carbonyl and aromatic CC signal near 1,725 (1,723) and 1,510 cm(-1) in the FT-IR spectra. X-ray diffraction studies showed that the two modified amylopectins lost the ordered A-type crystalline structure, characteristic of maize amylopectin. The encapsulation capacity of curcumin (ECC) in 1mg/mL CL-FAP microemulsion was measured at 88.13 μg/mg by HPLC.

Keywords: Cross-linked feruloyl amylopectin; Curcumin encapsulation; Pickering emulsion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amylopectin / chemical synthesis
  • Amylopectin / chemistry*
  • Chromatography, High Pressure Liquid
  • Coumaric Acids / chemistry*
  • Curcumin / chemistry*
  • Drug Compounding*
  • Oxidation-Reduction
  • Solubility
  • Spectroscopy, Fourier Transform Infrared
  • X-Ray Diffraction
  • Zea mays / chemistry

Substances

  • Coumaric Acids
  • Amylopectin
  • ferulic acid
  • Curcumin