Phytochemical Screening and Medicinal Potentials of the Bark of Dacryodes Edulis (G. Don) HJ

ntal A me na on ly ir ti v c n a l E C f h o e Journal of Environmental Analytical l Ogboru et al., J Environ Anal Chem 2015, 2:5 m a n i s r t DOI: 10.4172/2380-2391.1000158 u r y o J Chemistry ISSN: 2380-2391 Research article Open Access Phytochemical Screening and Medicinal Potentials of the Bark of Dacryodes edulis (G. Don) HJ Lam Ogboru RO1*, Okolie PL2 and Agboje I1 1Moist Forest Research Station, Forestry Research Institute of Nigeria, Benin-City, Edo State, Nigeria 2Delta State University, Abraka, Delta State, Nigeria Abstract The bark of Dacryodes edulis (G. Don) H.J Lam have been used over the years in rural communities across the tropical region for its medicinal potentials. Phytochemicals are bioactive constituents which are produced via secondary metabolism in relatively small amounts. To ascertain the phytochemical components responsible for the ethno-medicinal properties, a qualitative and quantitative screening of the bark of the tree was conducted. The phytochemical screening of the bark of Dacryodes edulis was sourced from benin city , south-south Nigeria revealed that alkaloids(18.13 mg/kg), Phenolic compounds (22.01 mg/kg), Flavenoids (60.91 mg/kg), Tannins (18.16 mg/kg), Saponins (3.16 mg/kg), Anthraquinones (12.16 mg/kg), Cardiac glycosides (0.81 mg/kg) and steroids (0.91 mg/kg) were significantly present in the sample. The presence of these phytochemicals gives credence to the medicinal benefits that the bark of this plant has been used for in the past years. Keywords: Dacryodes edulis, Phytochemical screening, Flavanoids, human against diseases. It is for this reason that this study will Anthraquinones, Tannins identify the bioactive components that are responsible for the medicinal properties of D. edulis. Introduction The objective of this study was to identify and examine the Dacryodes edulis (G. Don) H.J Lam, the African pear, is an medicinal benefits of the bark of Dacryodes edulis plant. evergreen fruit common to the central Africa and the gulf of guinea region [1]. It has a relatively short trunk and a deep dense crown. Materials and Methods It attains a height of 18-40 m in the forest but not exceeding 12 Collection of plant sample m in plantations. Dacryodes edulis preferably does well is a shady, humid, tropical forest. However it thrives well adaptively to Dacryodes edulis barks were gotten from a much matured tree variations in soil type, humidity, and temperature and day length. from a residential area in Benin-City (6° 18.1510’ N and 5° 37.2508’ The natural range extends from Angola in the south, Nigeria in the E), Edo state, Nigeria. Benin-city is within the tropical rainforest agro- North, Sierra Leone in the West and Uganda in the east. It is also ecological zone of Nigeria. The Bark of the plant was air dried at room cultivated in Malaysia [2]. Dacryodes edulis bears fruits which are temperature for about one month at Moist Forest Research Station, edible, meanwhile the bark, leaves, stems, and roots are used as Benin-City. local medicine against some diseases [3,4]. The bark of the plant Processing of plant samples is pale grey in color and rough with droplets of resin [5,6]. The bark decoction is used for treatment of dysentery and anemia. The The air dried bar samples where now pulverised to powder using a decoction is also used as a gargle or mouthwash, for tonsillitis, and ceramic mortar and pestle to obtain a powdered form of the plant were general oral hygiene [7-9]. Extracts from the root and bark have then stored in airtight containers. also been administered from the treatment of leprosy and also the bar and leaves are boiled together and added to many traditional Preparation of aqueous extract of plant samples medicines for malaria treatment. The bark is ground and mixed The aqueous extract from the bark of Daycryodes edulis plant with palm kernel oil for healing injuries. The leaves are compound sample was prepared by soaking 10 g of powdered samples in 200 with 5-8 pairs of leaflets. The flesh of the fruit is dark blue or violet. ml of distilled water for 12 hr. The extract was then filtered paper or The results of phytochemical screening of the fruit, seed and leaves Whitman filter paper (Membrane, Glass, etc.). has shown the presence of alkaloids, tannins, Saponins, cyanogen Phytochemical analysis glycosides, flavonoids and phytates [10,11]. Chemical tests were conducted on the aqueous extract of the bark Phytochemicals are biologically active, naturally occurring sample by using standard methods. chemical compounds found in all the parts of plants, which are useful to humans than those attributed to macronutrient and micronutrients. They protect plants from various diseases and *Corresponding author: Ogboru RO, Moist Forest Research Station, Forestry contribute also to plants aroma, flavor and color. In general plant Research Institute of Nigeria, Benin-City, Edo State, Nigeria, Tel: 08034519060; E-mail: [email protected] chemicals that protect plant cells from environmental hazards such stress, pathogenic attack, forms of pollution drought and Received August 18, 2015; Accepted August 26, 2015; Published August 31, UV exposure are known as phytochemicals. These compounds 2015 are known as secondary metabolites and have various biological Citation: Ogboru RO, Okolie PL, Agboje I (2015) Phytochemical Screening and properties which makes many people in Nigeria use the various Medicinal Potentials of the Bark of Dacryodes edulis (G. Don) HJ Lam. J Environ Anal Chem 2: 158. doi:10.4172/2380-2391.1000158 plants for medicinal purposes. There are more than a thousand known and unknown phytochemicals. It is also well known that Copyright: © 2015 Ogboru RO, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits plants produce these chemicals to protect themselves, but recent unrestricted use, distribution, and reproduction in any medium, provided the researches demonstrate that many phytochemicals can also protect original author and source are credited. J Environ Anal Chem Volume 2 • Issue 5 • 1000158 ISSN: 2380-2391 JREAC, an open access journal Citation: Ogboru RO, Okolie PL, Agboje I (2015) Phytochemical Screening and Medicinal Potentials of the Bark of Dacryodes edulis (G. Don) HJ Lam. J Environ Anal Chem 2: 158. doi:10.4172/2380-2391.1000158 Page 2 of 3 Qualitative Analysis on Phytochemical Constituents Tannins Test for tannins Quantity of tannins was determined by using the spectrophotometer method. 0.5 g of plant sample is weighed into a 50 ml plastic bottle. 50 Half gram of powdered sample of each was boiled in 20 ml of distilled ml of distilled water is added and stirred for 1 hr. The sample is filtered water in a test tube and then filtered. The filtration method used here is the into a 50 ml volumetric flask and made up to mark. 5 ml of the filtered normal method, which includes a conical flask and filter paper. 0.1% FeCl2 sample is then pipette out into test tube and mixed with 2 ml of 0.1M was added to the filtered samples and observed for brownish green or a FeCl3 in 0.1M HCl and 0.008M K4Fe(CN)6.3H2O. The absorbance is blue black coloration, which shows the presence of tannins. measured with a spectrophotometer at 395 nm wavelength within 10 Tests for Saponins mins. Two grams of powdered samples of the plant was boiled together Saponins with 20 ml of distilled water in a water bath and filtered. 10 ml of the Twenty grams of powdered back of plant sample was put in a conical filtered sample was mixed with 5 ml of distilled water in a test tube and flask and 100 ml of 20% 2C H5OH was added to the plant sample. The shaken vigorously to obtain a stable persistent froth. The frothing was sample was heated over a hot bath for 4 hr with continuous stirring at then mixed with three drops of olive oil and observed for the formation about 550°C. The mixture is then filtered and the residue re-extracted of emulsion, which indicates the presence of Saponins. with another 200 ml of 20% C2H5OH. The combined extracts are Test for flavonoids reduced to 40 ml over a water bath at about 900°C. The concentrated solution was then transferred into a 250 ml separator funnel and 20 A few drops of 1% NH solution was added to the aqueous extract of 3 ml of (CH3CH2)2O is added to the extract and shaken vigorously. The each plant sample seen in a test tube. A yellow coloration was observed aqueous layer is recovered while the (CH3CH2)2O layer is discarded if flavonoids compounds are present. and the purification process is repeated. 60 ml of n-C4H9OH is added and the combined n-C H OH extracts is washed twice with 10 ml of 5% Test for cardiac glycosides 4 9 NaCl. The remaining solution is then heated in a water bath and after One ml of concentrated H2SO4 was prepared in a test tube. 5 ml evaporation; the samples are dried in the oven to a constant weight. of aqueous extract from each plant sample was mixed with 2 ml of Flavonoid glacial CH3CO2H containing one drop of FeCl3. The above mixture was carefully added to the 1 ml of concentrated H2SO4 so that the Ten grams of the plant sample is repeatedly extracted with 100 ml concentrated H2SO4 was underneath the mixture. If cardiac glycoside is of 80% aqueous methanol at room temperature. The whole solution is present in the sample, a brown ring will appear, indicating the presence then filtered through filter paper and the filtrate is later on transferred of the cardiac constituent.

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