In this study, phenolic compounds from Crithmum maritimum L. n-butanol soluble fraction were quantified and identified spectrophotometrically and by using HPLC-DAD technics. They equally investigated for their antioxidant potential utilizing six in vitro assays: DPPH • , ABTS •+ , O 2 •-, Bleaching of β-carotene in linoleic acid, CUPRAC and Ferric reducing power. High amounts of total phenolics and flavonoids were recorded: 161.57± 0.479 µg GA eq .mg -1 and 31.56± 0.291 µg Q eq .mg -1 respectively. Nine compounds among them hydroxicinnamic acid and hydroxybenzoic acid derivatives, coumarins and flavonoids were identified. Chlorogenic acid known for their various pharmacological properties was detected as major compound of the extract. Rutin, vanillin, ellagic acid, ferrulic acid,6,7 dihydroxy coumarin, methyl 1,4 benzoquinone and trans-cinnamic acid were also detected. The extract was found to exhibit strong antioxidant capacities in all systems. Based on these results, it is right to conclude the n-butanol extract is promising source of natural antioxidants.Atlantic coast [9,11]. In Algeria, the genus Crithmum is represented by only the species C.maritimum L. [12]. Researches on this species demonstrated the presence of essential oils [11], phenolic compounds [13][14][15][16], Vitamins and minerals [17,18], proteins and amino acids [19] and fatty acids [20].The soluble phenolic constituents of the n-butanol fraction from C. maritimum L. have not been studied previously. The present research aimed to identify and quantified phenolic components present in the n-butanol extract from aerial parts of C.maritimum L. in full flowering stage using Folin Ciocalteu, aluminum chloride and HPLC-DAD analysis and to determine their antioxidant potential by different methods: DPPH • , ABTS •+ and O 2•scavenging, lipid peroxidation, ferric reducing power and CUPRAC.
Material and methods Plant materialAerial parts of marine fennel (Crithmum maritimum L.) were collected in August 2016 at full flowering stage, in the region of Jijel North eastern of Algeria (36°47′16.33″ N Lat., 5°38′53.45″ E Long. and 3 m altitude). A voucher specimen (ZA / 144) was deposited at the laboratory of Biomolecules and Plant Breeding, FeCl 3 (0.1%) were added to the mixture. Absorbance was measured at 700 against a blank (methanol). Results were given as absorbance and compared with those of BHT and BHA used as positive controls.
Cupric reducing capacity (CUPRAC)The cupric reducing antioxidant capacity was determined using the method of Apak et al.[30] modified by Öztürk et al. [31] A mixture constituted for 60 µL ammonium acetate buffer (1M, pH 7.0), 50 µL of 7.5 mM neocuproin and 50 µL 10 mM (Cu Cl 2 , 2H 2 O) was prepared and then 40 µL of sample solution at concentrations (6.25-200) µg/mL was added to the initial mixture. After one hour of incubation at room temperature, the absorbance at 450 nm was read against a blank reagent. Standard antioxidants used in this test were BHT and BHA. Results were given as absorbance and A 0.5 (µg/mL) values cor...