Penentuan konsentrasi hambat minimal (KHM) dan onsentrasi bunuh minimal (KBM) ekstrak Propolis terhadap biofilm bakteri Porphyromonas gingivalis

Background: Porphyromonas gingivalis become one gram negative bacteria found in endodontic infections. Porphyromonas gingivalis is a persistent microorganisms that can cause failure of root canal treatment, because the bacteria can form biofilms that are more resistant microorganisms defense against...

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Bibliographic Details
Main Authors: Maria Istiqomah Marini, Dian Agustin Wahjuningrum, Febriastuti Cahyani
Format: Article PeerReviewed
Language:Indonesian
Indonesian
Indonesian
Published: Fakultas Kedokteran Gigi Universitas Airlangga 2014
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Online Access:http://repository.unair.ac.id/95283/1/17.%20CD-4-2-2014-01766-fp.pdf
http://repository.unair.ac.id/95283/2/17.Penentuan%20konsentrasi%20hambat%20minimal%20%28KHM%29%20dan%20konsentrasi%20bunuh%20minimal%20%28KBM%29%20ekstrak%20Propolis%20terhadap%20biofilm%20bakteri%20Porphyromonas%20gingivalis.pdf
http://repository.unair.ac.id/95283/3/17.validasi%20%28The%20Deteminan%20of%20MIC%29.pdf
http://repository.unair.ac.id/95283/
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Institution: Universitas Airlangga
Language: Indonesian
Indonesian
Indonesian
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Summary:Background: Porphyromonas gingivalis become one gram negative bacteria found in endodontic infections. Porphyromonas gingivalis is a persistent microorganisms that can cause failure of root canal treatment, because the bacteria can form biofilms that are more resistant microorganisms defense against antibiotics and the immune response. Back to nature, there is alternative material, one of them is propolis. Propolis active compounds like flavonoids, essential oils, terpenoids, saponins, and propolis ethanolic extracts are significant to exhibited antimicrobial activity. Propolis antimicrobial effects is directly proportional to its concentration. Purpose: The aim of this study is to know the minimalinhibitory concentration (MIC) and minimal bactericidal oncentration (MBC) of propolis extract against biofilm of Porphyromonas gingivalis. Method: This study was an in-vitro experimental research laboratory with the post test only control group design. Propolis extracted by ethanol 70% on maceration method and dilute into several concentrations. Value of MIC and MBC were done by counting the biofilm bacteria colony in Tryptic Soy Agar (TSA) with Drop Plate Miles Misra method. Growth of bacteria colonies is calculated manually in colony forming unit (CFU)/ml. Result: There was no effect from the smallest concentration to the biggest concentration of propolis extract against biofilm of Porphyromonas gingivalis. Conclusion: There wasn`t MIC and MBC of propolis extract to the biofilm of Porphyromonas gingivalis.