Antioxidant capacities of vetiver (
Vetiveria zizanioides) oil were evaluated by two different in vitroassays: the DPPH
free radical scavenging assay and the Fe
2+-metal chelating assay. Results showedthat the vetiver oil (VO) possessed a strong free radical scavenging activity when compared to standardantioxidants such as butylated hydroxytoluene (BHT) and
-tocopherol. However, its metal chelatingcapacity was relatively weak. VO (10
L/mL) dissolved in methanol exhibited ~93% free radicalscavenging activity in the DPPH
assay and ~34% Fe
2+ chelating activity in the metal chelating assay.By contrast, 10 mM BHT and 0.1 mM
-tocopherol exhibited 93 and 89% free radical scavengingactivities in the DPPH
assay, respectively, and 1 mM EDTA exhibited ~97% activity in the metalchelating assay. Among the complex constituents in the crude VO,
-vetivenene,
-vetivone, and
-vetivone, which had shown strong antioxidant activities, were isolated and identified using variouschromatographic techniques including silica gel open column chromatography, silica HPLC, and GC-MS. These results show that VO and some of its inherent components can be potential alternativenatural antioxidants.Keywords: Vetiver oil;
Vetiveria zizanioides; antioxidant activity; DPPH; terpenoids; vetivone