Research Article - (2020) Volume 3, Issue 2
Qualitative and Quantitative Phytochemical Composition of Brachystegia Eurycoma Root, Leaf and Stem Bark
2Department of Zoology, Ahmadu Bello University Zaria, Kaduna State, Nigeria
Received Date: Apr 11, 2020 / Accepted Date: Apr 18, 2020 / Published Date: May 02, 2020
Copyright: ©Copyright: ©2020 Akande O A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
This study assesses the phytochemical screening of Brachystegia eurycoma root, leaf and bark using aqueous solvent. Phytochemical screening was conducted to determine the presence of natural products (alkaloids, tannins, steroid, saponin, phenol, carbohydrate, flavonoid, terpenoid, triterpenoids, quinone and cardial glycoside) using standard procedure. The qualitative phytochemical constituents of Brachystegia eurycoma leaf, root and stem bark revealed the presence Alkaloid, Flavonoid, quinone, tannin, saponin and Terpenoids while Phenol, carbohydrate, steroids and triterpenoids are absent in the leaf, stem bark and root extracts of the plant. Cardiac glycoside was only present in root extracts. The quantitative phytochemical screening of the extracts showed that they had high concentrations of alkaloids and tannins and they were relatively low in Terpenoids. The results evidently specifies aqueous extract of leaf, bark and root of Brachystegia eurycoma contains various bioactive compounds which have various medicinal properties that can be used for the treatment of many diseases. However, isolation of individual phytochemical constituents and subjecting it to the biological activity will definitely provide more fruitful results. Therefore, it is recommended as a plant of phytopharmaceutical importance.
Keywords
Brachystegia eurycoma, Phytochemicals, Quantitative, QualitativeIntroduction
Plants plays crucial role in sustaining humanity, plants have not only provided humankind with food, clothing, flavours, cosmetics, ornamental, fumigants, insect deterrents and fragrance, but also served humanity in the treatment of ailment [1]. The importance of plants cannot be overemphasized. Many chemical substances are responsible for the usefulness of plants. For instance reported that the medicinal value of plants lies in the chemical (bioactive) substances present in the plants [2]. Plants contain a number of chemicals that are very important to many industries. Two major industries that have benefitted from the chemicals found in plants are the food processing and pharmaceutical industries. Progress in the study of plant chemistry has led to diverse research in the development of novel products that are useful to man. Reported that the search for biologically active agents is a part of a wider renaissance of scientific significance to bring in new chemotherapeutics [3]. Their usage as traditional health remedies is the most popular for about 80% of the world population in Asia, Latin America and Africa and it is reported to have minimal side effects [4, 5]. Some of these chemical substances found in plants also have protective roles. For instance, stated that plants protect themselves through a chemical defensive system [6]. Plants also contain a number of specialized chemical substances that serves as the major internal constituents controlling growth and development. Houghton noted that plants synthesize very complex molecules with specific stereochemistry and can show biological activity with new modes of action [7]. Brachystegia eurycoma is an economic tree crop that grows in the tropical rainforest of West Africa [8]. In some parts of Nigeria Brachystegia eurycoma is known as “achi” in Igbo land, “akalada” in Yoruba, “Akpakpa or apaupan” in Ijaw, “dewen” in Benin, “okwe” in Edo, “okung” in Efiki [9].
The plant has been found to have potential medicinal and domestic uses, and is a traditional food plant in Africa. This little known seed help improve nutrition, boost food security, foster rural development and support sustainable land scare [9]. The seed gum from Brachystegia eurycoma compared favorably with commercial gums used in the food industry and can be used as a binding agent in tablet formulation [10]. In some cultures, the seed flour is used as soup thickening and stabilizing agent and as emulsifying agent in food systems [11, 12]. Unegbu reported that in Nigeria, the main culinary use of gum from Brachystegia eurycoma is in thickening soups [9]. Phytochemical screening determines the presence of biologically active ingredients that the plants contains. These compounds such as alkaloids, tannins, cardiac glycosides, terpenoids, saponins, anthraquinones, flavonoids, saponins and so on are the major basis of pharmacological activities of medicinal plants. Harish reported that global demand for alkaloids and their derivatives as well as other bioactive compounds has grown substantially [13]. The presence of many secondary metabolites in plants and plant products have been shown to display potent activity against infectious organisms and potency in treating diseases [14]. Therefore this study aim to determine the phytochemicals composition of Brachystegia eurycoma leave, root and bark.
Methodology
Healthy Brachystegia eurycoma root, leaf and stem bark were collected from the Old Oyo National Park, Nigeria and was identified and authenticated at the herbarium of the Department of Botany, Ahmadu Bello University and Zaria, Nigeria. The plant was washed under running tap water to eliminate dust and other foreign particles. The root, leaves and stem bark were dried under shade at room temperature. The dried root, leaves and stem bark were crushed to powder with in an electric mill. Two gram each of B. eurycoma root, leaf and stem bark powder was cold macerated in 20ml of distilled water for 24 hours with constant shaking and filtered using Whitman’s filter paper No. 1. It was then concentrated to dryness on water bath at 40°C and the crude extract was kept in refrigerator. Qualitative and quantitative phytochemical test involved the simple chemical test to detect the secondary metabolites using standard method of Trease and Evans [15].
Results and Discussion
The qualitative phytochemical constituents of B. eurycoma leaf, stem bark and root were revealed in Table1, it revealed that Alkaloid, Flavonoid, quinone, tannin, saponin and Terpenoids are present in the leaves, stem bark and root of B. eurycoma. The table further reveal that Phenol, carbohydrate, steroids and triterpenoids are absent in the leaf, stem bark and root extracts of the plant. Cardiac glycoside was only present in root extracts. Table2 revealed the quantitative phytochemical composition of B. eucrycoma leaf, stem bark and root, in which alkaloid and tannin recorded the highest composition for both leaf, stem bark and root extracts (8.24±0.09, 6.34±0.05 and 5.47±0.02) (7.08±0.04, 4.36±0.02 and 2.09±0.05) while Terpenoids recorded the least (0.77±0.01, 0.65±0.01 and 0.49±0.02).
Table1: Qualitative Phytochemical screening of Brachystegia eurycoma Leaf, Stem Bark and Root
|
Parameters |
Leaf |
Stem Bark |
Roots |
|
Alkaloid |
++ |
++ |
++ |
|
Flavonoid |
++ |
++ |
++ |
|
Phenol |
-- |
-- |
-- |
|
Quinone |
++ |
++ |
++ |
|
Carbohydrate |
-- |
-- |
-- |
|
Cardial Glycoside |
-- |
-- |
++ |
|
Saponin |
++ |
++ |
++ |
|
Tannin |
++ |
++ |
++ |
|
Steroid |
-- |
-- |
-- |
|
Triterpenoids |
-- |
-- |
-- |
|
Terpenoids |
++ |
++ |
++ |
Key
• ++ means Present
• -- means absent
Table2: Quantitative Phytochemical screening of Brachystegia eurycoma Leaf, Stem Bark and Root
|
Parameters |
Leaf |
Stem Bark |
Roots |
|
Alkaloid |
8.24±0.09a |
6.34±0.05a |
5.47±0.02a |
|
Flavonoid |
3.32±0.07b |
2.97±0.03c |
2.02±0.05b |
|
Quinone |
1.46±0.03c |
1.04±0.01c |
1.23±0.02c |
|
Cardial Glycoside |
0.00±0.00e |
0.00±0.00e |
0.41±0.01d |
|
Saponin |
1.82±0.03c |
1.51±0.05c |
1.22±0.01c |
|
Tannin |
7.08±0.04a |
4.36±0.02b |
2.09±0.05b |
|
Terpenoids |
0.77±0.01d |
0.65±0.01d |
0.49±0.02d |
Means followed by the same superscript in each row are not significant (P<0.05).
Discussion
Phytochemical screening have been reported to aid in the assessment of plants chemical constituents and also for the search of plant bioactive ingredients that could be used in the production and formulation of drugs [16]. Phytochemical screening of the leave, root and bark of Braschystegia eurycoma revealed the presence of Alkaloid, Flavonoid, Quinone, Tannin, Saponin and Terpenoids as the major phytochemical components. The presence of these bio-active constituents, alkaloids, saponins, flavonoids, tannis and terpenoid in the extract of Brachystegia eurycoma leave, bark and root clearly indicates the phyto-therapeutic potentials of this plant. The qualitative and quantitative phytochemical evaluation of bioactive chemical compounds of the plants extract is in accordance with the report of [12].
Flavonoids are a group of polyphenols compounds found in fruits and vegetables and in many plant parts have multiple biological activities [17, 18]. Ao reported that Flavonoids has vasodilators, anticarcinogenic, anti-inflammatory and antibacterial activities while Cowan reported the anti-allergic, antiviral, estrogenic and immune system stimulating effects of flavonoids [19, 20]. Alkaloids are reported as a plant bases that exhibit certain physiological properties when used in herbal medicine [20]. Most of them have anti-malarial, antifungal and antimicrobial activities [21]. Tannins in plants are known to improve healing of ulcers and burns, and also known for their antioxidant and antimicrobial properties. It possesses astringent properties and is thought to act as inhibitors of oxidative phosphorylation and electron transport (by depletion of iron); thus depriving bacteria of iron [21]. Saponin are group of glycosides that is widely distributed in higher plants. They are characterized by forming colloidal solution in water, which froth upon shaking. They have bitter taste and drugs containing them are usually irritating to the mucous membranes. Thus, these compounds give a permanent froth when shaken with water. Saponins destroy the red blood cells by hemolysis and are toxic especially to cold blooded animals. Many have been used as fish poisons and are toxic to aquatic life. Tannins are astringent, bitter plant polyphenols that either bind and precipitate or shrink proteins. The astringency from the tannins is what causes the dry and puckery feeling in the mouth following the consumption of red wine or an unripened fruit. Their main function in nature seems to be one of protection; animals are deterred from eating plants high in tannins because of the bitter, astringent. Tannins have traditionally been considered antinutritional but it is now known that their beneficial or antinutritional properties depend upon their chemical structure and dosage [22]. Recent studies have demonstrated that products containing chestnut tannins included at low dosages (0.15-0.2 %) in the diet can improve wellbeing [14].
Conclusion and Recommendation
The findings revealed that aqueous leaf, bark and root extract of Brachystegia eurycoma contains various bioactive compounds which have various medicinal properties that can be used for the treatment of many diseases. However, isolation of individual phytochemical constituents and subjecting it to the biological activity will definitely give fruitful results. Therefore, it is recommended as a plant of phytopharmaceutical importance [23, 24].References
- Activity of Phytochemicals from Acacia Nilotica, Entada Africana and Mimosa Pigra Linn on Salmonella Typh. Journal of Animal and Plants Sciences. 10: 1248-1258.
- Cchetri H P, Yogol N S, Shernan J, Anupa K C, Mansoor S, et al. (2008). Phytochemical and Antimicrobial Evaluations of Report and Opinion. Kathmandu University Journal of Science, Engineering and Technology 1: 49-54.
- Moundipa F P, Njayou F N, Yanditoum S, Sonke B, Mbiapo T F (2001) Medicinal Plants Used in the Bamoun Region (West Cameroon) Against Jaundice and Other Liver disorders. Cameroon Journal of Biological and Biochemical Sciences 2: 39-46.
- Bibith B, Jisha V K, Salitha C V, Mohan S, Valsa A K (2002) Antibacterial Activity of Different Plant Extracts. Indian Journal of Microbiology 42: 361-363.
- Maghrani M, Zeggwah N, Michel J, Eddoukas M (2005) Antihypertensive Effect of Lepidium Sativum in Spontaneous Hypertensive Rats. Journal of Ethnopharmacology 102: 193-197.
- Vanwyk B, Gerricke N (2000) Peoples Plants: A Guide to Useful Plants of Southern Africa. Briza Publications, Pretoria 2000: 48-53.
- Houghton P J (1996) Compound with Anti-HIV Activity from Plants. Transactions Royal Society Tropical Medicine Hygiene 90: 601-604.
- Uzondu A L, Nwadike K N, Okoye E I (2014) Application of Brachystegia eurycoma Gum-Egg Albumen Mixture in the Formulation of Modified Release Metronidazole Tablets. International Journal of Pharmaceutical Sciences and Drug Research 6: 109-113.
- Unegbu C C, Njoku S C, Ajah O, Chima V (2016) The Effect of Processing Time on the Proximate and Phytochemical Composition of Brachystegia eurycoma. Ijrdo - Journal of Biological Science 2: 11-23.
- Uzomah A, Ahiligwo R N (1999) Studies on the rheological properties and functional potentials of achi (Brachystegia eurycoma) and ogbono (Irvingia gabonensis) seed gums. Food Chem 67: 217-222.
- Olayemi O, Jacob O (2011) Preliminary evaluation of Brachystegia eurycoma seed mucilage as tablet binder. Int J Pharm Res Inno 3: 1-6.
- Uhegbu F O, Onwuchekwa C C, Iweala E E, Kanu I (2009) Effect of processing methods on nutritive and antinutritive properties of seeds of Brachystegia eurycoma and Detarium microcarpum from Nigeria. Pakistan J Nutri, 8: 316-320.
- Harish C A, Rawal R S, Rawat M S, Bhatt I D, Vijay K P (2010)Analysis of Berberine Content Using HPTLC Fingerprinting of Roots and Bark of Three Himalaya Berberis species. Asian Journal of Biotechnology 2: 239-2010.
- Schiavone A, Guo K, Tassone S, Gasco L, Hernandez E, et al. (2007) Effects of a Natural Extract of Chestnut Wood on Digestibility, performance Traits, and Nitrogen Balance of broiler Chicks. Poultry Science 87: 521-527.
- Trease G E, Evans W C (2009) Trease and Evans Pharmacognosy, 16th Ed. New York, Saunder’s Elsevier Ltd 2009: 104-262.
- Yakubu M T, Akanj M A, Oladiji A T (2005) Aphrodisiac potentials of aqueous extract of Fadogia agrestis (Schweinf Ex Heirn) stem in male albino rats. Asian J. Androl 7: 399-404.
- Steffan B, Watjen W, Michels G, Niering P, Wray V (2005) Polyphenols from plants used in traditional Indonesian medicine (Jamu): Uptake and antioxidative effects in rat H4IIE hepatoma cells. J. Pharm Pharmacol 57: 233-240.
- Cushnie T P T, Lamb A J (2005) Antimicrobial activity of flavonoids. Int. J. Antimicrob. Agents 26: 343-356.
- Ao C, Li A, Elzaawely A A, Xuan T D, Tawata S (2008) Evaluation of antioxidant and antibacterial activities of Ficus microcarpa L. fil. Extract. Food Control 19: 940-948.
- Cowan M (1999) Plant products as antimicrobial agents. Clin. Microbiol. Rev 12: 564.
- Scalbert A (1991) Antimicrobial properties of tannins. Phytochemistry 30: 3875-3883.
- Muller Harvey I, McAllan A B (1992) Tannins: Their biochemistry and nutritional properties. Advances in Plant Cell Biochemistry and Biotechnology 1: 151-217.
- Aiyelagabe O O (2000) Antimicrobial activity of Jatropha multifida roots. Fitoterapia 72: 544-546.
- Igwe O U, Okwu D E (2013) Phytochemical composition and antiinflammatory activities of Brachystegia eurycoma seeds and stem bark. Der pharma chemical 5: 224-228.
