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Activities of Ficus fistulosa Leave Extract and Fractions against Hepatitis C Virus
- Source :
- Procedia Chemistry. 18:179-184
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Hepatitis C Virus (HCV) is a major global disease which often leads to chronicity and is potential to liver failure. There is no anti-HCV vaccine and the high diversity of viral genotypes will probably make it very difficult to develop a vaccine. Therefore, the development of new drugs for HCV treatment is highly required. It is commonly known that numerous important modern drugs have been developed from molecules originally isolated from natural sources. In this study, we tested the leave extract and fractions of Ficus fistulosa for their anti-HCV activities by cell culture method using Huh7it cells and HCV JFH1a. The result showed that ethanol extract of Ficus fistulosa (FFL) inhibited HCV JFH1a with IC50 value of 20.43±4.51μg/ml. Toxicity test also indicated that FFL was not toxic with CC50 value of >200μg/ml. The extract was further fractionated using chloroform (FFLC) and butanol (FFLB) successively. FFLC showed anti-HCV activity with IC50 value of 5.67±1.54μg/ml and CC50 value of >100μg/ml (Selectivity index >17.65). Further separation of FFLC by open column chromatography resulted in 12 subfractions (FFLC1-C12). Two subfractions, FFLC10, and FFLC11 showed high selectivity index (>100) with IC50 value of 0.60±0.30μg/ml and 0.43±0.29μg/ml, respectively. Therefore the leave extract (FFL) and fractions (FFL10, FFL11) of Ficus fistulosa would be a good candidate to develop antiviral against HCV.
- Subjects :
- 0301 basic medicine
Hepatitis C Virus
Ethanol
Chloroform
Chemistry(all)
Traditional medicine
Hepatitis C virus
Butanol
030106 microbiology
General Medicine
medicine.disease_cause
03 medical and health sciences
chemistry.chemical_compound
Column chromatography
chemistry
Toxicity
antiviral activity
Chemical Engineering(all)
medicine
Ficus fistulosa
IC50
Subjects
Details
- ISSN :
- 18766196
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Procedia Chemistry
- Accession number :
- edsair.doi.dedup.....f2dbea83c0904581559b227e6ef6d187
- Full Text :
- https://doi.org/10.1016/j.proche.2016.01.028