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  1. Home
  2. Browse by Author

Browsing by Author "Hassan, H. S."

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    Evaluation of Antimicrobial and Antioxidant Activity of β-Sitosterol-3-O-Glucoside Isolated from Lannea Kerstingii Engl. & K. Krause (Anacardiaceae)
    (Federal University Gusau-Nigeria, 2016) Njinga, N. S.; Sule, M. I.; Pateh, U. U.; Hassan, H. S.; Magaji, M. G.; Abdullahi, S. T.; Bakare-Odunola, T. M.; Bawa, B.; Egharevba, G. O.; Shittu, A. O.
    β-sitosterol-3-O-glucoside was isolated using dry vacuum liquid chromatography. It was characterized using 1H-NMR, 13C-NMR and 2D NMR spectra. The antimicrobial activity was determined using agar diffusion method. The minimum inhibitory concentration (MIC) and minimum bactericidal/fungicidal concentration (MBC/MFC) were determined using broth dilution method. Antioxidant activity was determined through reaction of compound with DPPH radical. The compound was active against S. aureus, Methicillin Resistant Staphylococcus aureus, P. mirabilis, S. typhi, K. pneumoniae, E. coli, B. subtilis, C. albicans and C. tropicalis with zone of inhibition ranging from 22.0 ± 0.4 to 34.0 ± 0.3 mm and inactive against P. aeroginosa, Proteus vulgaris and C. krusei. The MIC ranged from 25.0 to 50.0 μg/ml while the MBC/MFC ranged from 50.0 to 200.0 μg/ml. The % DPPH scavenging activity at 4.0x103 μg/ml was found to be 81.44 ± 0.41 %. This result shows the high antioxidant and wide spectrum antimicrobial activity of β-sitosterol-3-O-glucoside which can be a potential lead drug for resistant bacteria such as MRSA, and a potential source of natural antioxidants.
  • Item
    Evaluation of antimicrobial and antioxidant activity of β-Sitosterol-3-O-Glucoside isolated from Lannea Kerstingii Engl. & K. Krause (Anacardiaceae).
    (International Journal of Science for Global Sustainability. Published by the Federal University, Gusau, Nigeria., 2016-03) Njinga, N. S.; Sule, M. I.; Pateh, U. U.; Hassan, H. S.; Magaji, M. G.; Abdullahi, S. T.; Bakare-Odunola, T. M.; Bawa, B.; Egharevba, G. O.; Shittu, A. O.
    β-sitosterol-3-O-glucoside was isolated using dry vacuum liquid chromatography. It was characterized using 1H-NMR, 13C-NMR and 2D NMR spectra. The antimicrobial activity was determined using agar diffusion method. The minimum inhibitory concentration (MIC) and minimum bactericidal/fungicidal concentration (MBC/MFC) were determined using broth dilution method. Antioxidant activity was determined through reaction of compound with DPPH radical. The compound was active against S. aureus, Methicillin Resistant Staphylococcus aureus, P. mirabilis, S. typhi, K. pneumoniae, E. coli, B. subtilis, C. albicans and C. tropicalis with zone of inhibition ranging from 22.0 ± 0.4 to 34.0 ± 0.3 mm and inactive against P. aeroginosa, Proteus vulgaris and C. krusei. The MIC ranged from 25.0 to 50.0 μg/ml while the MBC/MFC ranged from 50.0 to 200.0 μg/ml. The % DPPH scavenging activity at 4.0x103 μg/ml was found to be 81.44 ± 0.41 %. This result shows the high antioxidant and wide spectrum antimicrobial activity of β-sitosterol-3-O-glucoside which can be a potential lead drug for resistant bacteria such as MRSA, and a potential source of natural antioxidants.
  • Item
    Phytochemical, antibacteria and anticonvulsant activity of the stem bark of Lannea kerstingii Engl & K. Krause (Anacadiaceae).
    (Journal of Pharmacy and Bioresources. Published by the Faculty of Pharmaceutical Sciences, University of Jos., 2018) Njinga, N. S.; Sule, M. I.; Shittu, A. O.; David, M. S.; Amali, M. O.; Bolaji, A. R.; Abdullahi, S. T.; Hassan, H. S.; Atunwa, S. A.; Eniayewu, O. I.
    The stem bark of Lannea kerstingii Engl. & K. Krause was investigated for its phytochemistry, acute toxicity, antibacterial and anticonvulsant activit ies. Standard methods were used to evaluate phytochemistry while antibacterial activity was determined using agar diffusion and broth dilution method s on Staphylococcus aureus, Salmonella typhii, Pseudomonas aeruginosa, Klebsiella pneumonia, Proteus vulgaris, Escherichia coli and Bacillus subtilis. Maximal electroshock-induced seizures test in chicks and pentylenetetrazole-induced seizures test in mice were used to determine the anticonvulsant activity. Phytochemical studies revealed the presence of flavonoids, tannins, carbohydrates steroids and triterpenes. Ethyl acetate and methanol fractions of the stem bark were found to be active against S. aureus, S. typhi, P. aeruginosa, K. pneumoniae, Proteus sp, E. coli, Bacillus subtilis with zone of inhibition ranging from 20-27.5mm and MIC ranging from 6.25mg/mL to 100mg/mL and MBC from 50mg/mL and above. LD50 was found to be 2154.066 mg/kg. The crude methanol extract of the stem bark afforded dose (150, 300 and 600mg/kg) dependent protection to the laboratory animals against the hind limb tonic extension though not statistically significant (P<0.05) showing the inability of the extract to inhibit seizure discharge within the brainstem seizure substrate. Meanwhile the extract at doses of 300 and 600mg/kg significantly (P<0.05) prolonged the onset of seizure in pentylenetetrazole (PTZ) test showing the potential of this plant in raising seizure threshold in the brain therefore making it beneficial in the treatment of myoclonic and absence seizures. This justifies the use of the plant in treating convulsion.

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