Research Article

Seasonal Variation in Essential Oils Composition and the Biological and Pharmaceutical Protective Effects of Mentha longifolia Leaves Grown in Tunisia

Table 1

Yields extracts, amounts of total flavonoids, total phenolic compounds, and determined IC50 values of the DPPH free radical scavenging assay of M. longifolia leave extracts and essential oil. Ascorbic acid was used as positive control.

ExtractsYield ()TPC
mg GAE/g
TF
mg QE/g
DPPH
IC50 (g/ml)
carotene
IC50 (g/ml)

Ml EtOH-H2OE12.4659.25±0.3818.23±0.3516.23 ± 1.6066.75± 0.57
Ml HexF7.35ndnd> 1000>1000
Ml EtAOcF2.599.72±1.2620.85 ± 0.9412.64± 0.2134.75 ± 0.76
Ml WF2.6145.25 ± 0.8710.75 ± 0.4747.71± 0.4356.31± 0.67
E-E0.5-2.5--> 100> 100
Ascorbic acid---3.50-

TPC: total phenolic content; TF: flavonoid content.
mg GAE /g: mg of gallic acid equivalent per g of dry plant extract.
mg QE/g: mg of quercetin equivalent per g of dry plant extract.
IC50 (μg/ml): the IC50 values corresponding to the amount of extract required to scavenge 50 % of radicals present in the reaction mixture.
nd: not detected.
E: essential oil extracted at winter season; E: spring essential oil.