Effects of different chemical modifications on the antioxidant activities of polysaccharides sequentially extracted from peony seed dreg

Int J Biol Macromol. 2018 Jun:112:675-685. doi: 10.1016/j.ijbiomac.2018.01.216. Epub 2018 Feb 6.

Abstract

Four types of sequentially extracted peony seed dreg polysaccharides (PSDPs) fractions were modified through sulfation, phosphorylation and carboxymethylation and studied for their in vitro antioxidant characteristics. The modified derivatives showed decreased sugar and protein content, while uronic acid content was elevated as compared to native (un-modified) polysaccharides. Further, modified derivatives shared the similar maximum absorption peaks indicating their homogeneous nature. The Fourier transform infrared (FTIR) spectra of sulfated, carboxymethylated and phosphorylated derivatives showed that hydroxyl groups were converted to OS, COO and POH bonds, respectively. The sulfated polysaccharides (S-PSDPs) displayed the highest reducing ability [S-CASS (1.854)], DPPH radical scavenging ability [S-CASS (95.07%)] and ABTS radical scavenging activity [S-CASS (99.85%)]. The phosphorylated polysaccharides (P-PSDPs) exhibited maximum hydroxyl radical scavenging activity [P-DASS (92.61%)] and ferrous ion chelating ability (99.94% for all the fractions). The carboxymethylated polysaccharides (C-PSDPs) maintained moderately stable antioxidant ability. Overall, the four different PSDPs modified by the same chemical method also resulted into different chemical composition, characteristic absorption peaks and antioxidant attributes. We conclude that the different modifications of the polysaccharide fractions had their own potential significance as new antioxidants for food industry and human health.

Keywords: Antioxidant attributes; Chemical modification; Peony seed dreg polysaccharides; Sequential extraction.

MeSH terms

  • Antioxidants / pharmacology*
  • Benzothiazoles / chemistry
  • Biphenyl Compounds / chemistry
  • Free Radical Scavengers / chemistry
  • Hydroxyl Radical / chemistry
  • Ions
  • Iron Chelating Agents / pharmacology
  • Oxidation-Reduction
  • Paeonia / chemistry*
  • Picrates / chemistry
  • Polysaccharides / isolation & purification*
  • Polysaccharides / pharmacology*
  • Seeds / chemistry*
  • Spectrophotometry, Ultraviolet
  • Spectroscopy, Fourier Transform Infrared
  • Sulfonic Acids / chemistry

Substances

  • Antioxidants
  • Benzothiazoles
  • Biphenyl Compounds
  • Free Radical Scavengers
  • Ions
  • Iron Chelating Agents
  • Picrates
  • Polysaccharides
  • Sulfonic Acids
  • 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid
  • Hydroxyl Radical
  • 1,1-diphenyl-2-picrylhydrazyl