Antioxidant Activities of Some Cameroonian Plants Extracts Used in the Treatment of Intestinal and Infectious Diseases

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In continuation of evaluating in vitro biological activities of Cameroonian medicinal plants extracts [1] , we report here the antioxidant activities of Cameroonian plants used in the treatment of infectious and intestinal diseases: Pittosporum mannii (Pittosporaceae), Vepris heterophylla (Rutaceae) and Ricinodendron heudelotii (Euphorbiaceae).
Pittosporum mannii Hook f. (syn. of P. viridifl orum Sims, P. abyssinicum Delile var.angolense Oliv., P. fl oribundum Wight and Arn., P. dalzielii Hutch.fi de Friis) is a shrub widely spread in the savannah zone of Adamawa, in the highlands of West Cameroon and mount Mandara [2] .Known as Bourangal in Bororo language, ground internal part of dried bark is given to young child against stomach worm diseases.It is also used in traditional medicine to treat fever, malaria, inflammation and stomach ache and as antidote for insect bites [3][4][5] .A number of investigations have been performed on P. mannii indicating that its leaves possess antimicrobial properties and contains compounds such as volatiles monoterpenes, sesquiterpenes, and cytotoxic saponins [3,6,7] .
A survey of literature revealed no report of antioxidant activities on these plants.The aim of this present investigation was to screen the antioxidant properties and to determine if the uses in traditional medicine for treatment of intestinal and infectious diseases can be substantiated through in vitro experiments.
Samples of all the above medicinal plants were authentifi cated at the National Herbarium, Yaounde.Vouchers are kept in the herbarium of laboratories of botany of the Department of Biological sciences of the Faculty of Science of the University of Ngaoundere, Cameroon.
Air dried and ground stem bark of P. mannii (1.05 kg) collected from Bafang, West province, Cameroon, was macerated in 5 l of MeOH/CH 2 Cl 2 (1+1) at room temperature for 72 h.The filtrate was then evaporated to dryness under reduced pressure at 60°.The same operation was repeated three times to give a total extract of 256 g.The residue mixed with 300 ml of water was extracted with ethyl acetate.After concentration as mentioned above, the organic fraction yielded 57 g of ethyl acetate extract which was then extracted with chloroform.
Air-dried and pulverized leaves (500 g) and twigs (150 g) of V. heterophylla collected from Tokombere in the far North region of Cameroon near the city of Ngaoundere, Cameroon in October 2006 were extracted at room temperature successively with hexane, ethyl acetate and MeOH.Each time, 100 g of plant material and 3×100 ml of solvent were stirred at 3000 rpm for 4 h.The fi ltrates were then concentrated to dryness under reduced pressure at 60° to yield respectively hexane (11.43Total phenolic compounds in the ethyl acetate (EA) extract of P. mannii and in the MeOH extract of V. heterophylla were determined with Folin-Ciocalteu reagent and calculated using gallic acid as the standard.Extracts (100 μl) were added to 50% Folin-Ciocalteau reagent (100 μl).After 3 min, 2 ml of 2% Na 2 CO 3 solution was added to the mixture, which was then left to stand for 30 min.Absorbance was measured at 750 nm on a spectrophotometer and compared to gallic acid calibration curves.The content of total phenolics is expressed as gallic acid equivalents (GAEs) [18] .All analyses were run in three replicates and averaged.
Five milligrams of dried extracts were dissolved in 10 ml of MeOH to make a stock solution of 0.5 mg/ ml.Different concentrations of extracts (500, 250, 200, 100, 50, 25 μg/ml) were prepared by dilution with methanol from this stock solution.DPPH radical scavenging activity of all extracts was determined according to a modifi ed version of De Beer et al [19] : 10 μl of each extract, standard Trolox solution (0.025-0.40 mM) or 10% methanol (positive control) was added to 200 μl of a 6.34 10 -5 M ethanol solution of DPPH; control was prepared without any extract and the absorbance of the reaction mixture at 520 nm was measured after fi ve minutes at 36.5° using a Tecan 5.01 microplates reader.All tests were run in triplicate and averaged.Radical scavenging was expressed as % inhibition of DPPH.
The ABTS scavenging activity of samples were measured according to the method used by Re et al [20] .An ABTS + (7 mM) in water was preincubated for at least 12 h with 2.45 mM (fi nal concentration) of K 2 SO 8 to produce the radical cation.The ABTS + solution was diluted with 96% ethanol to an absorbance of 0.70±0.02at 734 nm at 30°.Two hundred microliters of ABTS + solution was added to 10 μl of each extract concentration prepared as indicated above, standard Trolox solution (0.025-0.40 mM in EtOH 96%) or 10% methanol used as control.The absorbance of the mixture was determined in the Tecan 5.01 microplatereader after 240 s of incubation at 37°.The absorbance of the resulting oxidized solution was compared to that of the calibrated Trolox standard.Result were expressed in term of TEAC (Trolox equivalent antioxidant capacity) μg/ml.Assays of all samples were conducted in triplicated and averaged.TLC checks for alkaloids, for phenolics and for terpenoids for all extracts gives the results presented  1. TLC assay of these extracts spraying with 0.2% DPPH in 96% ethanol showed immediately many bleached bands for the EA extract of P. mannii and for the MeOH extract of V. heterophylla while the MeOH/dichloromethane (1+1) of R. heudelotii showed only few bands after hours.The best activity seen in the ethyl acetate extract of P. mannii and the result on methanol extract of V. heterophylla prompted us to examine the antioxidant activity of these two extracts.Results of the phenolic contents with respect of the percent of gallic acid equivalents (GAEs) showed that both extracts are rich in polyphenolic compounds.The EA extract of P. mannii was very rich in phenolic derivatives than the MeOH extract of V. heterophylla with 314±4 and 262±6 mg/g GAEs, respectively (Table 2).Based on the DPPH and ABTS radical scavenging assay the above results was confi rmed and quantifi ed, showing potent antioxidant properties of the EA extract of P. mannii and the MeOH extract of V. heterophylla.For both extracts, determination of IC 50 values in DPPH assay gives (177.39±0.55μg/ml) and (204.69±5.02μg/ml) for EA and MeOH extract respectively showing that they are respectively about eight and four time more effective than Trolox (939.19±2.44 μg/ml; higher value but lower antioxidant activity) use as standard compound (Table 3).The EA extract of P. mannii and the MeOH extract of V. heterophylla strongly scavenged    4 and 5).Results compared to Trolox; obviously due to content in phenolics.
These results are in agreement with those obtained by Gomez in 1983 while examining chemical constituents of Malian leaves of V. heterophylla [13] .To the best of our knowledge, this is the fi rst report of the presence of phenolic derivatives in P. mannii species and the antioxidant activity in the family Pittosporaceae.These results also showed difference in organic compounds contents of the Cameroonian species of P. mannii compared to the same species collected from other African countries such as Madagascar, Kenya and Mali.The genus Pittosporum (Pittosporaceae) investigated was shown for the fi rst time to display high antioxidant activity.Its high contains in phenolic derivatives might be responsible for the antioxidant activity and might explain its usage in the Cameroonian folk medicine for the treatment of malaria, intestinal diseases and infl ammations.
Leaves of R. heudelotii were collected from Buea, South West province, Cameroon in August 2006.Air-dried powdered leaves (1.00 kg) were extracted successively with ethyl acetate and MeOH/CH 2 Cl 2 (1+1) at room temperature.After removal of the solvent by concentration under reduced pressure at 60°, 57 g of ethyl acetate and 58 g of MeOH/CH 2 Cl 2 residue were obtained, respectively.Two milligrams of each extract were dissolved in 100 µl of the respective solvent.Twenty microliters of each solution were spotted on TLC silica gel plates F 254 and developed in different solvents system.For Alkaloids checking system used were, a polar extracts in hexane-ethyl acetate (60-40) and polar extracts in toluene:ethyl acetate:diethylamine (70:20:10).For phenolic compounds and fl avonoids,

TABLE 1 : QUALITATIVE EVALUATION OF ANTIOXIDANT ACTIVITY OF PLANTS EXTRACTS USING 0.2 % DPPH ETHANOLIC SOLUTION AS REVELATOR
++++ strong free radical scavenging properties, ++ mild radical scavenging properties, + weak free radical scavenging properties, -no bleaching of the plate spraying with DPPH solution, n.d.not evaluated, HE n-hexane extract, EA ethyl acetate extract, CHCl 3 chloroform extract, MeOH methanol extract while MeOH/ CH 2 Cl 2 is the methanol/dichloromethane (1+1) extract on Table

TABLE 3 : ANTIOXIDANT ACTIVITY OF MEOH EXTRACT OF V. HETEROPHYLLA AND ETHYL ACETATE EXTRACT OF P. MANNII IN DPPH TEST USING TROLOX AS STANDARD
a Values are mean of three experiments±SD

TABLE 4 : ANTIOXIDANT ACTIVITY OF ETHYL ACETATE EXTRACT OF P. MANNII IN ABTS TEST USING TROLOX AS STANDARD
a Values are mean of three experiments±SD.

TABLE 5 : ANTIOXIDANT ACTIVITY OF METHANOL EXTRACT OF V. HETEROPHYLLA IN ABTS TEST USING TROLOX AS STANDARD
a Values are mean of three experiments±SD, -not observed