Ascorbyl-6-O-oleate: A Bioconjugate Antioxidant Lipid
| dc.contributor.author | Perini, Ilaria | |
| dc.contributor.author | Ambrosi, Moira | |
| dc.contributor.author | Tanini, Damiano | |
| dc.contributor.author | Ninham, Barry | |
| dc.contributor.author | Capperucci, Antonella | |
| dc.contributor.author | Lo Nostro, Pierandrea | |
| dc.date.accessioned | 2023-01-16T22:39:44Z | |
| dc.date.issued | 2020 | |
| dc.date.updated | 2021-11-28T07:35:47Z | |
| dc.description.abstract | Ascorbyl‐6‐O‐oleate (Asc‐OL) was synthesized enzimatically and studied in the pure state and in aqueous dispersions. Small‐angle X‐ray scattering (SAXS), differential scanning calorimetry (DSC), Fourier transformed infrared (FTIR) spectroscopy experiments and antioxidant tests were conducted in order to characterize the compound and to evaluate its reducing properties. Asc‐OL is a bioconjugate molecule, in fact it combines the main physico‐chemical features of the two parent molecules, i. e. the redox and acidic properties of Vitamin C and the fluid‐like state of oleic acid. The appropriate tests were carried out to confirm the excellent radical scavenging activities of Asc‐OL, that turned out to be a promising candidate for the stabilization, transport and protection against radical attack of valuable hydrophobic active ingredients used in food and pharmaceutical formulations. | en_AU |
| dc.format.mimetype | application/pdf | en_AU |
| dc.identifier.issn | 2365-6549 | en_AU |
| dc.identifier.uri | http://hdl.handle.net/1885/282797 | |
| dc.language.iso | en_AU | en_AU |
| dc.publisher | Wiley | en_AU |
| dc.rights | © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim | en_AU |
| dc.source | ChemistrySelect | en_AU |
| dc.subject | antioxidant | en_AU |
| dc.subject | L-ascorbyl esters | en_AU |
| dc.subject | micelle(s) | en_AU |
| dc.subject | oleic acid | en_AU |
| dc.subject | Vitamin C | en_AU |
| dc.title | Ascorbyl-6-O-oleate: A Bioconjugate Antioxidant Lipid | en_AU |
| dc.type | Journal article | en_AU |
| local.bibliographicCitation.issue | 6 | en_AU |
| local.bibliographicCitation.lastpage | 1944 | en_AU |
| local.bibliographicCitation.startpage | 1938 | en_AU |
| local.contributor.affiliation | Perini, Ilaria, University of Florence | en_AU |
| local.contributor.affiliation | Ambrosi, Moira, University of Florence | en_AU |
| local.contributor.affiliation | Tanini, Damiano, University of Florence | en_AU |
| local.contributor.affiliation | Ninham, Barry, College of Science, ANU | en_AU |
| local.contributor.affiliation | Capperucci, Antonella, University of Florence | en_AU |
| local.contributor.affiliation | Lo Nostro, Pierandrea, University of Florence | en_AU |
| local.contributor.authoruid | Ninham, Barry, u7100478 | en_AU |
| local.description.embargo | 2099-12-31 | |
| local.description.notes | Imported from ARIES | en_AU |
| local.identifier.absfor | 340503 - Organic chemical synthesis | en_AU |
| local.identifier.ariespublication | u6269649xPUB567 | en_AU |
| local.identifier.citationvolume | 5 | en_AU |
| local.identifier.doi | 10.1002/slct.201903528 | en_AU |
| local.identifier.scopusID | 2-s2.0-85079719009 | |
| local.publisher.url | https://www.wiley.com/en-gb | en_AU |
| local.type.status | Published Version | en_AU |
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