scholarly journals Antibacterial activities of sawdust and stem bark of Sasswood tree (Erythrophleum suaveolens, Guill. & Perr. Brenan, 1917) extracts against selected wood bacteria

2020 ◽  
Vol 36 (2) ◽  
pp. 52-61
Author(s):  
D.O. Ekhuemelo ◽  
C. Ekhuemelo ◽  
E.T. Tembe

This study assessed the antibacterial properties of sawdust and stem bark of Erythrophleum suaveolens extracts on selected wood bacteria. Erythrophleum suaveolens samples were collected, dried and macerated by dissolving 1 Kg and 0.60 Kg of stem bark and sawdust respectively into 1 L of n-hexane, ethyl acetate and methanol. Sporfloxacin ciprofloxacin and cefuroxine antibiotics were used as control. The mixture was left for 24 hours then filtered and the filtrates evaporated to dryness. Qualitative phytochemical screening, zone of inhibition, minimum inhibitory and Bactericidal Concentrations (MIC/MBC) were determined according to standard methods. Tannins, steroids, saponins, glycosides, flavonoids, carbohydrates anthraquinones and alkaloids phytochemicals were present in E. suaveolens extracts. Zone of inhibition (32 – 37 mm) of antibiotics on test bacteria compared favourably with 17 – 24 mm of E. suaveolens extracts. Erythrophleum suaveolens ethyl acetate and methanol E. suaveolens extracts inhibited Staphylolococus aureus, Ralstonia solanacearum, Proteus mirabilis, Enterococcus faecium and Acidobacterium capsulatum growth at MIC of 10 mg/mL and n-hexane extracts at 20 mg/mL. At MBC of 20 mg/mL methanol stem bark extract completely killed most test bacteria. Methanol extracts were the most active extracts. The study has shown that E. suaveolens extracts can be explored in the control of plant diseases caused by test bacteria in the study. Key words: Antibacterial, E. suaveolens, extract, phytochemicals, zone of inhibition

2018 ◽  
Vol 24 ◽  
pp. 11-18
Author(s):  
M Hasanuzzaman ◽  
W Islam ◽  
MB Islam

Phytochemical screening of the secondary metabolites was performed with acetone, chloroform, methanol and n-hexane extracts of the leaves, roots, stem bark and seeds of the plant Syzygium cumini (Linn.) and were detected using various tests for identifying the isolated components. Acetone extract of the leaves showed the presence glycosides, phenols, proteins, resins and saponins while the stem bark extract showed the presence of alkaloids, flavonoids, glycosides, phenols, proteins, resins and saponins. All the above constituents except saponins were detected in the root extract. The seed extract contains alkaloids, carbohydrates, phenols, proteins and tannins. Chloroform extract of the leaves showed the presence of alkaloids, proteins and steroids while root extract contains alkaloids and steroids and that of seed extract alkaloids, carbohydrates, phenols, proteins and tannins, however, alkaloids and tannins were found in the stem bark extract. Methanol extract of the leaves and stem bark showed the presence of alkaloids, carbohydrates, flavonoids, glycosides, phenols, resins, saponins, steroids and tannins while the root extracts contain all the above constituents along with proteins. N-hexane extract of the leaves contain only alkaloids, roots contain alkaloids and resins and that of seeds contain carbohydrates and proteins while alkaloids, proteins and tannins were found in stem bark extract. The present findings reveal the presence of various medicinally important phytochemicals from the plant S. cumini extracts may have application in traditional system of medicine to cure various ailmentsJ. bio-sci. 24: 11-18, 2016


2020 ◽  
Vol 19 (2) ◽  
pp. 125-131
Author(s):  
Titumeer Al Fahad ◽  
Md Ruhul Kuddus ◽  
Choudhury M Hasan

The main objective of the current research was phytochemical and biological studies of the stem bark of Miliusa velutina (Dunal) Hook. f. & Thomson (Annonaceae). Four purified compounds i.e., friedelin, lupeol, β- sitosterone and caffeic acid were isolated by repeated chromatographic separation and purification of M. velutina. The compounds were identified by analysis of NMR spectral data. The crude dichloromethane extract of stem bark of M. velutina (DEMV) along with its Kupchan partitionates i.e., petroleum ether (PESF), ethyl acetate (EASF), chloroform (CSF) and aqueous (AQSF) soluble fraction were screened for antioxidant, cytotoxic, thrombolytic and antibacterial activities. During the antioxidant activity assay, the AQSF revealed maximum activity with IC50 value of 71.67 μg/ml. The cytotoxicity of plant samples was determined by brine shrimp lethality bioassay, where the maximum cytotoxic activity has been observed for EASF (LC90 = 9.01 μg/ml). In the thrombolytic activity test, the crude dichloromethane extract demonstrated significant efficacy with 46.27% inhibition of clot lysis. In antibacterial screening, the CSF exhibited noticeable inhibitory activity against Shigella boydii with the zone of inhibition 15 mm compared to the standard ciprofloxacin (zone of inhibition = 47 mm). Dhaka Univ. J. Pharm. Sci. 19(2): 125-131, 2020 (December)


2020 ◽  
Vol 4 (3) ◽  
pp. 247-251
Author(s):  
Z. Abdullahi ◽  
A. A. Jimoh ◽  
B. E. Patrick ◽  
M. I. Yakubu ◽  
D. Mallam

Different parts of Vitellaria paradoxa plant have many applications in ethno-medicine. Some of the uses of this plant include treatment of diarrhoea and other GIT disorders. In this study the antidiarrhoeal activity of the ethanol extract of Vitellaria paradoxa was evaluated using three experimental models: Castor oil-induced diarrhoea; small intestinal motility and intestinal fluid accumulation (enteropooling) models in mice. Five groups of five mice were used for each model. Group one mice received 10 ml/kg of distilled water, while groups 2, 3, and 4 received 125, 250 and 500 mg/kg of the extract orally respectively. Group 5 mice received Loperamide 5 mg/kg orally. Oral median lethal dose (LD50) of the extract was determined using OECD (2008) Guideline 425. Phytochemical studies were conducted using standard procedures. The LD50 was estimated to be greater than 5000 mg/kg body weight and there were no signs of mortality or visible signs of toxicity in all the mice treated. Phytochemical screening revealed the presence of carbohydrates, alkaloids, flavonoids, saponins, tannins, triterpenes, steroids, cardiac glycosides and anthraquinones glycosides. Extract showed a dose-dependent anti-diarrhoeal activity by reducing stool frequency and consistency. The extract at the higher doses significantly (p < 0.05) inhibited GIT motility and castor oil-induced enteropooling, comparable to that of the reference control drug Loperamide. The study showed that ethanol stem bark extract of Vitellaria paradoxa possess anti-diarrhoeal activity and thus justifies its ethno-medicinal use in the treatment of diarrhoea.


2020 ◽  
Vol 14 (5) ◽  
pp. 107-112
Author(s):  
Aliyu Ebbo Abdullahi ◽  
Teleh Elsa Abdullahi ◽  
Udok Etuk Emmanuel ◽  
Jengebe Ladan Muhammad ◽  
Alhaji Saganuwan Saganuwan

2014 ◽  
Vol 9 (18) ◽  
pp. 826-833 ◽  
Author(s):  
B. A. Akinpelu ◽  
O. A. Igbeneghu ◽  
A. I. Awotunde ◽  
E. O. Iwalewa ◽  
O. O. Oyedapo

2020 ◽  
Vol 9 (4) ◽  
pp. 218-223
Author(s):  
Godfrey Mutuma Gitonga ◽  
◽  
Joseph Ngeranwa ◽  
Alex King’ori Machocho ◽  
Silas Kiruki ◽  
...  

Author(s):  
C. E. Anarado ◽  
F. M. Chukwubueze ◽  
C. J. O. Anarado ◽  
N. L. Umedum ◽  
C. B. Nwanya

Aim: To compare the phytochemicals and antioxidant activities of stem bark and root extracts of Annona muricata. Methodology: The stem bark and root of Annona muricata were collected, washed, air-dried, ground and each extracted with methanol, ethyl acetate and n-hexane. The extracts were analysed for the presence of phytochemicals. Antioxidant screening was also carried out on the samples. Results: Cardiac glycosides were present in all the extracts of both root and stem bark. Alkaloids were present in moderate abundance in all the extracts except the ethyl acetate stem bark extract. Saponins and tannins were found in methanol extracts of both parts and also in very high abundance but the stem contained higher amount of saponins while alkaloids and tannins were found more in the root. Flavonoids were only found in the ethyl acetate stem bark extract.  Steroids were absent in all the extracts except n-hexane root extract. The root showed greater enzymatic antioxidant activities than the stem bark. The solvent polarity affected the phytochemical found in each extract.  The antioxidant activities of the catalase, superoxidase dismutase and glutathione peroxidase were significantly higher in the root of Annona muricata than in the stem. Conversely, peroxidase showed a significantly higher activity in the stem than in the root. Conclusion: The stem bark and root exhibited good antioxidant properties, so there is need to isolate the compounds responsible for antioxidant property exhibited by the plant parts.


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