In Vitro Antioxidant and Anti-Glycation Activity of Resveratrol and Its Novel Triester with Trolox.

anti-glycation antioxidant chemical stability resveratrol resveratrol derivative trolox

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
24 Dec 2020
Historique:
received: 04 12 2020
revised: 17 12 2020
accepted: 21 12 2020
entrez: 30 12 2020
pubmed: 31 12 2020
medline: 31 12 2020
Statut: epublish

Résumé

Resveratrol (RSV) is well known for its many beneficial activities, but its unfavorable physicochemical properties impair its effectiveness after systemic and topical administration; thus, several strategies have been investigated to improve RSV efficacy. With this aim, in this work, we synthesized a novel RSV triester with trolox, an analogue of vitamin E with strong antioxidant activity. The new RSV derivative (RSVTR) was assayed in vitro to evaluate its antioxidant and anti-glycation activity compared to RSV. RSVTR chemical stability was assessed at pH 2.0, 6.8, and 7.2 and different storage temperatures (5 °C, 22 °C, and 37 °C). An influence of pH stronger than that of temperature on RSVTR half-life values was pointed out, and RSVTR greatest stability was observed at pH 7.2 and 5 °C. RSVTR showed a lower antioxidant ability compared to RSV (determined by the oxygen radical absorbance capacity assay) while its anti-glycation activity (evaluated using the Maillard reaction) was significantly greater than that of RSV. The improved ability to inhibit the glycation process was attributed to a better interaction of RSVTR with albumin owing to its increased topological polar surface area value and H-bond acceptor number compared to RSV. Therefore, RSVTR could be regarded as a promising anti-glycation agent worthy of further investigations.

Identifiants

pubmed: 33374280
pii: antiox10010012
doi: 10.3390/antiox10010012
pmc: PMC7823449
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Sebastiano Intagliata (S)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Angelo Spadaro (A)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Miriam Lorenti (M)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Annamaria Panico (A)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Edy A Siciliano (EA)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Sabrina Barbagallo (S)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Benito Macaluso (B)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Shyam H Kamble (SH)

Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA.

Maria N Modica (MN)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Lucia Montenegro (L)

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Classifications MeSH