| Literature DB >> 30007612 |
Alejandra Bermúdez-Oria1, Guillermo Rodríguez-Gutiérrez1, Elisa Rodríguez-Juan1, Alejandro González-Benjumea2, Juan Fernández-Bolaños3.
Abstract
This study explored the interaction of pectin with 3,4-dihydroxyphenylglycol (DHPG), a potent phenolic antioxidant naturally found in olive fruit, via encapsulation into pectinate beads. MALDI TOF-TOF analysis supported the formation of complexes between DHPG and pectin. A combination of covalent bonds (ester bonds) and non-covalent interactions, mostly hydrogen bonding, were suggested as the cause of DHPG-pectin complex formation. Free radical scavenging assays confirmed that DHPG maintained its antioxidant activity after complexation and after a digestion simulated in vitro with gastric and intestinal fluids. Therefore, DHPG-pectin beads could reach the large intestine and contribute to a healthy antioxidant environment.Entities:
Keywords: 3,4-Dihydroxyphenylglycol; Antioxidant; Covalent binding; MALDI TOF-TOF MS; No-covalent binding; Phenol-pectin complex
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Year: 2018 PMID: 30007612 DOI: 10.1016/j.carbpol.2018.05.089
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381