Aktiviti anti helicobacter pylori ekstrak sepuluh spesies phyllanthus dengan memfokuskan ekstrak kloroform phyllanthus pulcher

dc.contributor.authorWan Ismail, Wan Iryani
dc.date.accessioned2015-07-30T05:35:45Z
dc.date.available2015-07-30T05:35:45Z
dc.date.issued2005
dc.description.abstractTen spesies of Phyllanthus were screened for their in-vitro anti Helicobacter · pylori activities using agar diffusion method. The species are P. debilis, P. niruri and P. urinaria, P. acidus, P. columnaris, P. emblica, P. myrtifolius, P. oxyphyl/us, P. pulcher and P. ·reticulates. For the first three species as listed above, the whole plants were used, while only the leaves were used for other species. The plants were sequentially extracted by hexane, chloroform and methanol using soxhlet. A total of 30 crude extracts from the plants were screened for their anti bacterial activities and toxicity using brine shrimp Artemia salina assay. Ten bacterial pathogen i.e. H. pylori, Enterobacter sp., Escherichia coli, E. coli (ATCC 25922), Pseudomonas stutzeri, Salmonella sp., Shigella boydii, Sh dysenteriae, Staphylococcus aureus and Vibrio cholerae were also included in the disc diffusion assay. Chloroform extract of P. pulcher was selected based on its selectivity, specificity and strong activity (largest inhibition zone 24.2 ± 1.2 mm) against H. pylori and non-toxicity against A. salina. The phytochemical screening results showed the occurrence of terpenoid in the chloroform extract of P. pulcher. The chloroform extract was fractionated into 30 fractions using the best solvent system i.e. chloroform (8): ethyl acetate (2) by column chromatography. These fractions were retested on H. pylori and other pathogens using disc diffusion assay and fraction 18 (F18) was found to be selective, specific and active against on H. pylori with the largest inhibition zone diameter (30.0 ± 0 mm). Further testing on A. salina revealed that it was non-toxic LC50 acute = 1.350 ± 0.1 mg/ml and LCso chronic = 1 .000 ± 0.1 mg/ml. The minimum inhibition concentration (MIG) test of F18 showed that the MIC50 and MIC90 were 4 J.Jg/ml and 256 J.Jg/ml respectively on 20 clinical isolates of H. pylori. The MIG for H. pylori (SJ 179) was 32 IJQ/ml. Using batch ~- ~culture of H. pylori in Eugon broth with or without F18 (control), monitoring H. pylori by colony counting method and direct count, and observing cellular changes by SEM and TEM, there was evidence that F18 caused direct killing of the culturable spiral cells and at 16 !Jg/ml caused cell leakage. By LC-MS and referring to the database, F18 tentatively contain 13-sitosterol and some fatty acids (methyl nonadecanoate and tripalmitin).en_US
dc.identifier.urihttp://hdl.handle.net/123456789/1059
dc.language.isootheren_US
dc.subjectHelicobacter pylorien_US
dc.subjectEkstrak kloroformen_US
dc.titleAktiviti anti helicobacter pylori ekstrak sepuluh spesies phyllanthus dengan memfokuskan ekstrak kloroform phyllanthus pulcheren_US
dc.typeThesisen_US
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