| Literature DB >> 27474665 |
Thammarat Aree1, Suchada Jongrungruangchok2.
Abstract
Green tea catechins are potent antioxidant for prevention of various free radical-related diseases. Their antioxidant properties can be improved by encapsulation in cyclodextrins (CDs). Four inclusion complexes of β-CD with (-)-epicatechin (EC), (-)-epigallocatechin (EGC), (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG) have been investigated using single-crystal X-ray diffraction analysis combined with full geometry optimization by DFT/B3LYP calculation and the DPPH assay, aiming to deepen the understanding on their structure-antioxidant activity relationship. Scrutinizing the inclusion structures and conformational changes of the four encapsulated epicatechins reveals the common host-guest stabilization scheme and the epicatechin conformational flexibility facilitating the enhancement of activity. Thermodynamic stability order derived from DFT calculation in vacuum fairly agrees with the order of improved antioxidant capacity deduced from the DPPH assay, β-CD-EGCG>β-CD-ECG>β-CD-EGC≈β-CD-EC.Entities:
Keywords: (–)-Epicatechin (PubChem CID: 72276); (–)-Epicatechin gallate (PubChem CID: 107905); (–)-Epigallocatechin (PubChem CID: 72277); (–)-Epigallocatechin gallate; (–)-Epigallocatechin gallate (PubChem CID: 65064); Antioxidant activity; DFT calculation; DPPH (PubChem CID: 2735032); DPPH assay; Ethanol (PubChem CID: 702); X-ray analysis; β-Cyclodextrin (PubChem CID: 444041); β-cyclodextrin
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Year: 2016 PMID: 27474665 DOI: 10.1016/j.carbpol.2016.05.113
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381