Advisor(s)
Abstract(s)
The present study reports for the first time the metabolite profile and antioxidant activity of aqueous
extract obtained from Dracaena draco L. leaf. Volatiles profile was determined by HS-SPME/GC-IT-MS,
with 34 compounds being identified, distributed by distinct chemical classes: 2 alcohols, 5 aldehydes,
16 carotenoid derivatives and 8 terpenic compounds. Carotenoid derivative compounds constituted
the most abundant class in leaf (representing 45% of total identified compounds). Phenolics profile was
determined by HPLC/DAD and 9 constituents were identified: 2 hydroxycinnamic acid derivatives – 5-
O-caffeoylquinic and 3,5-O-dicaffeoylquinic acids; 4 hydroxycinnamic acids – caffeic, p-coumaric, ferulic
and sinapic acids and 3 flavonol glycosides – quercetin-3-O-rutinoside, kaempferol-3-O-glucoside and
kaempferol-3-O-rutinoside. The most abundant phenolic compound is quercetin-3-O-rutinoside (representing
50.2% of total polyphenols). Organic acids composition was also characterised, by HPLC–UV
and oxalic, citric, malic and fumaric acids were determined. Oxalic and citric acids were present in higher
amounts (representing 47%, each). The antioxidant potential of this material was assessed by the ability
to protect against free radical-induced biomembrane damage, using human erythrocyte as in vitro model.
Leaf extract strongly protected the erythrocyte membrane from haemolysis (IC50 of 39 ± 11 lg/ml), in a
time- and concentration-dependent manner. This is the first report showing that D. draco leaf is a promising
antioxidant agent.
Description
Keywords
Dracaena draco leaf Volatiles Polyphenols Organic acids Haemolysis inhibition Antioxidant activity
Citation
Santos, R.P.; Mendes, L.S.; Silva, B.M.; Guedes de Pinho, P.; Valentão, P.; Andrade, P.B.; Pereira, J. A.; Carvalho, M. (2011). Phytochemical profiles and inhibitory effect on free radical-induced human erythrocyte damage of Dracaena draco leaf: A potential novel antioxidant agent. Food Chemistry. ISSN 0308-8146. 124:3, p. 927-934.
Publisher
Elsevier