The antioxidant activity of methanolic and ethyl acetate extracts from Lava
ndula vera MM cell culture were evaluated by the Schaal oven test in bulk s
unflower oil and by the DPPH radical method. The oil oxidation was followed
by measuring the quantity of primary oxidation products (peroxide value).
Authentic rosmarinic acid, caffeic acid and BHT were tested in parallel for
comparison. Ethyl acetate extract much better protected the oil from oxida
tion than methanolic extract and its antioxidant efficiency was comparable
to that of pure rosmarinic and caffeic acids and much stronger than that of
BHT. Both cell culture extracts and the authentic phenolic acids were much
stronger scavengers of DPPH free radical than BHT on an equimolar basis. (
C) 2001 Elsevier Science Ltd. All rights reserved.