Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity

Thesis (PhD (Pharmacology))--University of Pretoria, 2005.

Saved in:
Bibliographic Details
Other Authors: Medlen, Connie E.
Format: Thesis
Language:English
Published: University of Pretoria 2013
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613464600510464
access_status_str Open Access
author2 Medlen, Connie E.
author_browse Medlen, Connie E.
author_facet Medlen, Connie E.
collection Thesis
dc_rights_str_mv © 2005, University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Thesis (PhD (Pharmacology))--University of Pretoria, 2005.
format Thesis
id oai:repository.up.ac.za:2263/31313
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:36:34.044Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2013
publishDateRange 2013
publishDateSort 2013
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/31313 Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity Medlen, Connie E. bapela@up.ac.za Lall, Namrita Bapela, Nchinya Benedict UCTD Naphthoquinones Antimycobacterial activity Multidrug-resistant (MDR) Mycobacterium tuberculosis Methyljuglone Drug synergy and cytotoxicity Thesis (PhD (Pharmacology))--University of Pretoria, 2005. Three naphthoquinones (shinanolone, 7-methyljuglone and diospyrin) were isolated from the dried roots ofEuclea natalensis, a tree belonging to the family Ebeneceae. The isolated compounds were purified by silica gel column chromatography and high performance liquid chromatography (HPLC). Nuclear magnetic resonance (1H NMR) was used to confirm their structure and purity. The percentage yield of shinanolone, 7-methyljuglone and diospyrin were 0.16, 0.12 and 0.32 respectively. Isolated compounds were tested for their antimycobacterial activity against drug-sensitive and multidrug-resistant clinical strains of M. tuberculosis by both the radiometric BACTEC 460 method and the colorimetric Alamar blue method. In the extracellular environment 7-methyljuglone was found to be the most active isolated compound which exhibited a minimum inhibitory concentration (MIC) in the range of „T0.5 ƒ®0.2 ƒÝg/ml. The extracellular MICs of the isolated compounds and the control (rifampicin) were in agreement in both the BACTEC 460 and the Alamar blue method. Furthermore, the cytotoxic effects of the isolated compounds were tested on human lymphocytes, fibroblasts and macrophages using the MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide] assay. 7-Methyljuglone was slightly toxic against resting and stimulated human lymphocytes (IC50 3.97 and 3.46 ƒÝg/ml, respectively), but not toxic against fibroblasts and macrophages. Rifampicin, crude extract, shinanolone and diospyrin were not toxic at tested concentrations. The compound that showed the highest activity in the extracellular environment was tested for intracellular activity on blood monocyte-derived macrophages and the THP-1 macrophage cell line using the radiometric BACTEC 460 method. 7-Methyljuglone exhibited antimycobacterial activity at „T5 ƒ®2.5 ƒÝg/ml in the intracellular environment. In clinical practice a combination of various drugs is necessary to prevent the emergence of resistance; therefore the in vitro activity of the most active naphthoquinone, 7-methyljuglone, was determined in two-drug combinations with standard antituberculous drugs (rifampicin, isoniazid, ethambutol and streptomycin) against M. tuberculosis using the radiometric BACTEC 460 method. In two-drug combinations, addition of sub-MICs of 7-methyljuglone, in both the extracellular and intracellular environment, resulted in a four-to six-fold reduction in MICs of rifampicin and isoniazid with fractional inhibitory concentrations (FIC) ranging between 0.25 and 0.5, suggesting a synergistic interaction against drug-sensitive strains of M. tuberculosis. The ability of 7-methyljuglone to inhibit the growth of drug-sensitive and multidrug-resistant strains of M. tuberculosis and the ability to enhance the activity of standard antituberculous drugs in vitro indicate that 7-methyljuglone may serve as a promising lead compound for future drug development for the treatment ofM. tuberculosis infections. Pharmacology Restricted Health Sciences 2013-09-09T12:10:55Z 2006-09-29 2013-09-09T12:10:55Z 2006-05-05 2005 2006-09-29 Thesis Bapela, NB 2005, Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity, PhD thesis, University of Pretoria, Pretoria, viewed yymmdd < http://upetd.up.ac.za/thesis/available/etd-09292006-130917 / > http://hdl.handle.net/2263/31313 http://upetd.up.ac.za/thesis/available/etd-09292006-130917/ en © 2005, University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Naphthoquinones
Antimycobacterial activity
Multidrug-resistant (MDR)
Mycobacterium tuberculosis
Methyljuglone
Drug synergy and cytotoxicity
Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title_full Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title_fullStr Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title_full_unstemmed Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title_short Isolation of Naphthoquinones from the roots of Euclea Natalensis and their in vitro antimycobacterial activity and toxicity
title_sort isolation of naphthoquinones from the roots of euclea natalensis and their in vitro antimycobacterial activity and toxicity
topic UCTD
Naphthoquinones
Antimycobacterial activity
Multidrug-resistant (MDR)
Mycobacterium tuberculosis
Methyljuglone
Drug synergy and cytotoxicity
url http://hdl.handle.net/2263/31313
http://upetd.up.ac.za/thesis/available/etd-09292006-130917/