Research Article
Macrofilaricidal activity of the plant Plumbago indica/rosea in vitro
Article first published online: 24 JUL 2002
DOI: 10.1002/ddr.10056
Copyright © 2002 Wiley-Liss, Inc.
Additional Information
How to Cite
Mathew, N., Paily, K. P., Abidha, Vanamail, P., Kalyanasundaram, M. and Balaraman, K. (2002), Macrofilaricidal activity of the plant Plumbago indica/rosea in vitro. Drug Dev. Res., 56: 33–39. doi: 10.1002/ddr.10056
Publication History
- Issue published online: 24 JUL 2002
- Article first published online: 24 JUL 2002
- Manuscript Accepted: 9 JUN 2002
- Manuscript Received: 3 MAR 2002
Funded by
- International Foundation for Science (IFS), Stockholm, Sweden. Grant Number: F/2929-1
- Abstract
- References
- Cited By
Keywords:
- filariasis;
- antifilarial;
- Plumbagin;
- 1,4-naphthalenedione;
- Setaria digitata
Abstract
The macrofilaricidal property of the plant, Plumbago indica/rosea, was investigated in vitro against Setaria digitata, a filarial parasite of cattle. Adult worms were incubated in a medium containing crude extract at concentrations 0.05, 0.04, 0.02, and 0.01 mg mL−1 for various incubation periods of 30 min, 1 h, 2 h, and 6 h, respectively, at 37°C and the worm motility was compared with that of solvent control worms kept in drug-free medium. Complete inhibition of motility was observed for concentrations ranging from 0.02 to 0.05 mg mL−1, whereas in the control all the worms were active. Bioassay-guided fractionation of the crude extract by silica gel column chromatography resulted in the identification of a very active fraction. The activity of this fraction against adult worms was further confirmed by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide–formazan colorimetric assay, which gave >50% inhibition for the active fraction at concentrations 0.05, 0.002, 0.005, and 0.0006 mg mL−1 at 30 min, 1 h, 2 h, and 6 h incubation periods, respectively. The physical and chemical data obtained from melting point determination, thin-layer chromatography and high-performance liquid chromatography analysis and IR, 1HNMR, 13CNMR, and gas chromatography-mass spectrometry spectral analysis have indicated the chemical structure of the active molecule as 5-hydroxy-2-methyl-1,4-naphthalenedione (plumbagin). Drug Dev. Res. 56:33–39, 2002. © 2002 Wiley-Liss, Inc.

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