PERBANDINGAN DAYA HAMBAT BERBAGAI METODE REBUSAN DAN PERASAN DAUN SAMBILOTO (Andrographis paniculata, Ness) PADA PERTUMBUHAN Shigella dysenteriae SECARA In vitro

Main Author: BUDIMAN, TAUFIQ
Format: Thesis NonPeerReviewed Book
Bahasa: eng
Terbitan: , 2009
Subjects:
Online Access: http://eprints.umm.ac.id/1604/1/PERBANDINGAN_DAYA_HAMBAT_BERBAGAI_METODE_REBUSAN_DAN_PERASAN_DAUN_SAMBILOTO.pdf
http://eprints.umm.ac.id/1604/
ctrlnum 1604
fullrecord <?xml version="1.0"?> <dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><relation>http://eprints.umm.ac.id/1604/</relation><title>PERBANDINGAN DAYA HAMBAT BERBAGAI METODE REBUSAN DAN &#xD; PERASAN DAUN SAMBILOTO (Andrographis paniculata, Ness) PADA &#xD; PERTUMBUHAN Shigella dysenteriae SECARA In vitro</title><creator>BUDIMAN, TAUFIQ</creator><subject>Q Science (General)</subject><description>Sambiloto is the plants many known by the people and used as medicine for various diseases, include dysentery disease was caused by Shigella dysenteriae bacteria. Based on the active essence content, sambiloto leaf contain tannin and &#xD; flavonoid compound useful for anti bacteria substance. In general, Sambiloto leaf process was conducted the people by poached and pressed, so that it could be different effectively level to allay dysentery disease. &#xD; The research was conducted to find out resistivity of stew and distillation of sambiloto leaf toward the growth of Shigella dysenteriae and to find out comparison of stew and distillation resistivity of sambiloto leaf toward the growth of Shigella dysenteriae. This research was conducted for June 8th to July 2nd 2009 in the Bio Technology Laboratory Muhammadiyah University of Malang. The research type of this research was true experiment and the experiment designed used was Completely Randomized Designed (RAL). The method used in this research is stew method R1 (25gr sambiloto + 900ml aquades), R2 (25gr sambiloto + 600ml aquades), R3 (25gr sambiloto + 300ml aquades) and the distillation method P1 (25gr sambiloto + 900ml aquades), P2 (25gr sambiloto + 600ml aquades), P3 (25gr sambiloto + 300ml aquades). The antibiotic of tetracycline as Kp control positive and K0 control negative without treatment, with three times repetation, so that sample unit used were 24 units. The parameter used to see resistivity of stew and &#xD; distillation of sambiloto leaf was clear zone diameter at prolific Shigella dysenteriae. &#xD; The analysis result of one way variant significant rate 1% indicated that there is significant influence various method of stew and distillation of sambiloto leaf at the growth Shigella dysenteriae bacteria. Whereas distillation method P1 (25gr sambiloto + 900ml aquades), P2 (25gr sambiloto + 600ml aquades), P3 (25gr sambiloto + 300ml aquades) have resistivity at the growth Shigella dysenteriae were bigger than stew method R1 (25gr sambiloto + 900ml aquades), R2 (25gr sambiloto + 600ml aquades), R3 (25gr sambiloto + 300ml aquades).</description><date>2009</date><type>Thesis:Thesis</type><type>PeerReview:NonPeerReviewed</type><type>Book:Book</type><language>eng</language><identifier>http://eprints.umm.ac.id/1604/1/PERBANDINGAN_DAYA_HAMBAT_BERBAGAI_METODE_REBUSAN_DAN_PERASAN_DAUN_SAMBILOTO.pdf</identifier><identifier> BUDIMAN, TAUFIQ (2009) PERBANDINGAN DAYA HAMBAT BERBAGAI METODE REBUSAN DAN PERASAN DAUN SAMBILOTO (Andrographis paniculata, Ness) PADA PERTUMBUHAN Shigella dysenteriae SECARA In vitro. Other thesis, University of Muhammadiyah Malang. </identifier><recordID>1604</recordID></dc>
language eng
format Thesis:Thesis
Thesis
PeerReview:NonPeerReviewed
PeerReview
Book:Book
Book
author BUDIMAN, TAUFIQ
title PERBANDINGAN DAYA HAMBAT BERBAGAI METODE REBUSAN DAN PERASAN DAUN SAMBILOTO (Andrographis paniculata, Ness) PADA PERTUMBUHAN Shigella dysenteriae SECARA In vitro
publishDate 2009
topic Q Science (General)
url http://eprints.umm.ac.id/1604/1/PERBANDINGAN_DAYA_HAMBAT_BERBAGAI_METODE_REBUSAN_DAN_PERASAN_DAUN_SAMBILOTO.pdf
http://eprints.umm.ac.id/1604/
contents Sambiloto is the plants many known by the people and used as medicine for various diseases, include dysentery disease was caused by Shigella dysenteriae bacteria. Based on the active essence content, sambiloto leaf contain tannin and flavonoid compound useful for anti bacteria substance. In general, Sambiloto leaf process was conducted the people by poached and pressed, so that it could be different effectively level to allay dysentery disease. The research was conducted to find out resistivity of stew and distillation of sambiloto leaf toward the growth of Shigella dysenteriae and to find out comparison of stew and distillation resistivity of sambiloto leaf toward the growth of Shigella dysenteriae. This research was conducted for June 8th to July 2nd 2009 in the Bio Technology Laboratory Muhammadiyah University of Malang. The research type of this research was true experiment and the experiment designed used was Completely Randomized Designed (RAL). The method used in this research is stew method R1 (25gr sambiloto + 900ml aquades), R2 (25gr sambiloto + 600ml aquades), R3 (25gr sambiloto + 300ml aquades) and the distillation method P1 (25gr sambiloto + 900ml aquades), P2 (25gr sambiloto + 600ml aquades), P3 (25gr sambiloto + 300ml aquades). The antibiotic of tetracycline as Kp control positive and K0 control negative without treatment, with three times repetation, so that sample unit used were 24 units. The parameter used to see resistivity of stew and distillation of sambiloto leaf was clear zone diameter at prolific Shigella dysenteriae. The analysis result of one way variant significant rate 1% indicated that there is significant influence various method of stew and distillation of sambiloto leaf at the growth Shigella dysenteriae bacteria. Whereas distillation method P1 (25gr sambiloto + 900ml aquades), P2 (25gr sambiloto + 600ml aquades), P3 (25gr sambiloto + 300ml aquades) have resistivity at the growth Shigella dysenteriae were bigger than stew method R1 (25gr sambiloto + 900ml aquades), R2 (25gr sambiloto + 600ml aquades), R3 (25gr sambiloto + 300ml aquades).
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