V6a-amylose helical cavity and benzoic acids with para-hydroxyl structure facilitate the formation of inclusion complex

Carbohydr Polym. 2022 Dec 15:298:120065. doi: 10.1016/j.carbpol.2022.120065. Epub 2022 Sep 3.

Abstract

Benzoic acids are always unstable during thermal processing. Herein, effects of typical molecular structure of benzoic acids and V-amylose on the formation and thermostability of inclusion complexes were investigated. Interestingly, the helical structure of six V-amylose transformed to V6a-amylose after complexing with four benzoic acids. Encapsulation efficiency (EE) and loading efficiency (LE) results presented that gentisic acid (DA) complexed with V6a-amylose achieving the highest EE of 79.76 % and LE of 7.25 %. X-ray diffraction (XRD) and differential scanning calorimetry (DSC) results demonstrated that DA, protocatechuic acid (PA), and gallic acid (GA) formed VI inclusion complexes with V-amylose, especially V6a-amylose-DA inclusion complexes with the highest crystallinity, while p-hydroxybenzoic acid (PHBA) was difficult to complex with V-amylose. Moreover, V6a-amylose-DA inclusion complexes showed the highest capacity in protecting the antioxidant activity from thermal processing. This suggested both V6a-amylose helical cavity and benzoic acids with para-hydroxyl structure facilitated the formation of thermostable inclusion complexes.

Keywords: Amylose helical structure; Benzoic acids; Structure; Thermal stability.

MeSH terms

  • Amylose* / chemistry
  • Antioxidants
  • Benzoates*
  • Gallic Acid
  • Hydroxybenzoates
  • X-Ray Diffraction

Substances

  • Antioxidants
  • Benzoates
  • Hydroxybenzoates
  • Gallic Acid
  • Amylose