EventsThe 19th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session b. Bioorganic, Medicinal and Natural Products Chemistry of the event The 19th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Oct, 2015
Citation
Pritam Juvatkar, Sandeep Waghulde, Pravin Naik, Nilesh Gorde, Antimicrobial activity of bark of Moringa oleifera L., in Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2015, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-19-b001
Share
Email
Facebook
Twitter
LinkedIn

Antimicrobial activity of bark of Moringa oleifera L.

Pritam Juvatkar 1
Nilesh Gorde 1
1. Research Student, Hon’ble Loksevak Madhukarrao Chaudhari College of Pharmacy, Faizpur, Dist: Jalgaon; Maharashtra, India
Abstract

Antimicrobial activity of different extracts of bark of Moringa oleifera was studied against ten bacterial strains These bacteria are both gram +ve and gram -ve. Bark were extracted with a petroleum ether, chloroform, ethyl acetate, ethanol and aqueous . In the present work the antibacterial activity was done by cup plate method. The antibacterial activity was expressed as zone diameter in millimeters. Different extracts from bark of the plant was compared with standards like benzyl penicillin for gram +ve bacteria and streptomycin for gram –ve bacteria using DMF as control. The readymade media for inoculum and culture was obtained from Himedia labs. Prepared herbal extracts from the bark of the plant were screened against bacteria organisms at the concentration range between 50 µg and 300 µg/0.1ml. The present investigation reveals that the aqueous, chloroform and ethyl acetate extracts and in some cases petroleum ether extract showed significant antimicrobial activity when compared with standard.

Keywords
Moringa species
antibacterial
soxhlet extraction
streptomycin
benzyl penicillin
gram +ve
Manuscript
Ultrasound-promoted One-Pot, Three Component Synthesis Of Novel 5-Amino-2-(4-Chlorophenyl)-7- Substituted Phenyl-8,8a-Dihydro-7H-[1,3,4]Thiadiazolo[3,2-A]Pyrimidine-6-Carbonitrile Derivatives.
Interest of 3-arylcoumarins as xanthine oxidase inhibitors