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Indian pluceha (Pluchea indica L.) is one of plant which has been used for many years as traditional <br /> <br /> medicine in Indonesia. Indian pluchea leaves are well-known for its ability to deodorize body. <br /> <br /> However, recent studies prove that Indian pluchea le...

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Main Author: YUNITA EKASARI NIM : 10714014, RIMA
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/30499
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:30499
spelling id-itb.:304992018-07-02T07:53:48Z#TITLE_ALTERNATIVE# YUNITA EKASARI NIM : 10714014, RIMA Indonesia Final Project INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/30499 Indian pluceha (Pluchea indica L.) is one of plant which has been used for many years as traditional <br /> <br /> medicine in Indonesia. Indian pluchea leaves are well-known for its ability to deodorize body. <br /> <br /> However, recent studies prove that Indian pluchea leaves is potentially able to perform as <br /> <br /> antibacterial agent to bacteria infecting skin, such as Propionibacterium acnes and Staphylococcus <br /> <br /> epidermidis. This research was aimed to identify and isolate the compound which contained <br /> <br /> antibacterial activity in Indian pluchea leaves. The crude drug of Indian pluchea leaves was <br /> <br /> extracted by reflux method using increasing polarity solvents, n-hexane, ethyl asetate and ethanol. <br /> <br /> All extracts were monitored using thin layer chromatography. Antibacterial activity of three extract <br /> <br /> were each being tested by using disk diffusion method, microdilution, and bioautography test. <br /> <br /> Based on disk diffusion test, all extracts had inhibiton zones for both of bacteria tests. Microdilution <br /> <br /> test results showed that all extract had MIC value >4096 µg/mL for both bacteria test. <br /> <br /> Bioautography test results indicated that all extract inhibition zone in Propionibacterium acnes and <br /> <br /> not obvious in Staphylococcus epidermidis. Ethanol extract was chosen for fractination as it had the <br /> <br /> highest zone of inhibition in disk diffusion test and clear inhibition zone in bioautography test. Rf <br /> <br /> 0,6 used as a guideline for isolating antibacterial compound. Fractionation method was vacuum <br /> <br /> liquid chromatography and purifying method was preparative TLC. The result indicated that one of <br /> <br /> was classified as flavonoid and another could not be identified. Both of isolate had antibacterial <br /> <br /> activity. <br /> text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Indian pluceha (Pluchea indica L.) is one of plant which has been used for many years as traditional <br /> <br /> medicine in Indonesia. Indian pluchea leaves are well-known for its ability to deodorize body. <br /> <br /> However, recent studies prove that Indian pluchea leaves is potentially able to perform as <br /> <br /> antibacterial agent to bacteria infecting skin, such as Propionibacterium acnes and Staphylococcus <br /> <br /> epidermidis. This research was aimed to identify and isolate the compound which contained <br /> <br /> antibacterial activity in Indian pluchea leaves. The crude drug of Indian pluchea leaves was <br /> <br /> extracted by reflux method using increasing polarity solvents, n-hexane, ethyl asetate and ethanol. <br /> <br /> All extracts were monitored using thin layer chromatography. Antibacterial activity of three extract <br /> <br /> were each being tested by using disk diffusion method, microdilution, and bioautography test. <br /> <br /> Based on disk diffusion test, all extracts had inhibiton zones for both of bacteria tests. Microdilution <br /> <br /> test results showed that all extract had MIC value >4096 µg/mL for both bacteria test. <br /> <br /> Bioautography test results indicated that all extract inhibition zone in Propionibacterium acnes and <br /> <br /> not obvious in Staphylococcus epidermidis. Ethanol extract was chosen for fractination as it had the <br /> <br /> highest zone of inhibition in disk diffusion test and clear inhibition zone in bioautography test. Rf <br /> <br /> 0,6 used as a guideline for isolating antibacterial compound. Fractionation method was vacuum <br /> <br /> liquid chromatography and purifying method was preparative TLC. The result indicated that one of <br /> <br /> was classified as flavonoid and another could not be identified. Both of isolate had antibacterial <br /> <br /> activity. <br />
format Final Project
author YUNITA EKASARI NIM : 10714014, RIMA
spellingShingle YUNITA EKASARI NIM : 10714014, RIMA
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author_facet YUNITA EKASARI NIM : 10714014, RIMA
author_sort YUNITA EKASARI NIM : 10714014, RIMA
title #TITLE_ALTERNATIVE#
title_short #TITLE_ALTERNATIVE#
title_full #TITLE_ALTERNATIVE#
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url https://digilib.itb.ac.id/gdl/view/30499
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