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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16362
Title: REPORT Phytochemical screening and antimicrobial activities of red silk cotton tree (Bombax ceiba L.)
Authors: Syed Sadaqat Shah
Syed Salim Shah
Arshad Iqbal
Sajjad Ahmed
Khan, Wisal Muhammad
Saddam Hussain
Li, Zhijian
Keywords: Phytochemical screening
antimicrobial activity
bacteria
fungi
Issue Date: 30-May-2018
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi
Citation: Shah, S. S., Shah, S. S., Iqbal, A., Ahmed, S., Khan, W. M., Hussain, S., & Li, Z. (2018). Phytochemical screening and antimicrobial activities of red silk cotton tree (Bombax ceiba L.). Pakistan Journal of Pharmaceutical Sciences, 31(3).
Abstract: The present study was conducted to investigate the phytochemical screening and antimicrobial activities of stem bark of Bombax ceiba L. The methanol extract was subjected to qualitative phytochemical screening using standard procedures. The results indicated the presence of alkaloids, tannins, glycosides, reducing sugar, saponins, phlobatanins and terpenoids. The antimicrobial activity was measured by disc diffusion method. Data revealed that Pseudomonas aeruginosa was inhibited by both methanol and ethanol extracts at the concentration of 2mg disc-1 {21.8mm (68.12%) and 21.3mm (66.56%)}. Similarly, methanol extract reduced the growth of Bacillus subtilis by 17.1mm (74.34%) at the concentration of 1 mg disc-1. However, ethanol extract showed a good activity of 18mm (121.6%) and 20.6mm (112.5%) against Xanthomonas maltophilia at concentrations of 1 and 2 mg disc-1, respectively. Aqueous extract showed 16 mm (53.33% Z.I) against Escherichia coli at 2 mg disc-1. Klebsiella pneumoniae was found resistant to all of the three extracts, while the growth of Candida albicans was inhibited by methanol through 16.5 mm (58.92% Z.I) at 1 mg disc-1. The above study concluded the medicinal potential of B. ceiba.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/16362
ISSN: 1011-601X
Appears in Collections:Issue 03

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