AKTIVITAS ANTIVIRUS EKSTRAK ETANOL RIMPANG Zingiber officinale Rosc. DAN Curcuma heyneana Val & Zijp. TERHADAP HEPATITIS C VIRUS SECARA IN VITRO
Hepatitis C infection is a global world problem. The cronically infection has infected around 71 million people that caused serious morbidity. Hepatitis C treatment is still limited, due to high treatment costs and some drugs have experienced resistance. Therefore, the new agent for anti hepatit...
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Format: | Theses and Dissertations NonPeerReviewed |
Language: | English English English Indonesian |
Published: |
2019
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Subjects: | |
Online Access: | http://repository.unair.ac.id/90755/1/FF.FT.17-19%20Lay%20a%20abstrak.pdf http://repository.unair.ac.id/90755/2/FF.FT.17-19%20Lay%20a%20daftar%20isi.pdf http://repository.unair.ac.id/90755/3/FF.FT.17-19%20Lay%20a%20daftar%20pustaka.pdf http://repository.unair.ac.id/90755/4/FF.FT.17-19%20Lay%20a.pdf http://repository.unair.ac.id/90755/ |
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Institution: | Universitas Airlangga |
Language: | English English English Indonesian |
Summary: | Hepatitis C infection is a global world problem. The cronically
infection has infected around 71 million people that caused serious
morbidity. Hepatitis C treatment is still limited, due to high treatment costs
and some drugs have experienced resistance. Therefore, the new agent for
anti hepatitis C is needed. This study examined antihepatitis C activity from
ethanol extract of Z. officinale rhizome Sand C. heyneana by in vitro culture
cells. Both of them possessed a potential antihepatitis C virus activities with
the IC50 values of 0.16±0.89 μg/mL and 0.19±1.23 μg/mL, respectively,
without any toxicity effect, the CC50 of Z. officinale was 61.73 μg/mL and
C. heyneana was 147.04 μg/mL. The target mechanism of extract were
found that ethanol extract of Z. officinale rhizome inhibit at the post-entry
step of hepatitis C virus life cycle, while ethanol extract of C. heyneana
rhizome inhibit at the entry and post-entry step. These results indicated that
Z. officinale and C. heyneana may potential to be developed for antihepatitis
C agents. |
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