Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten
Background. The incidence of Multi Drug Resistant (MDR) in extraintestinal E. coli has become a global problem in the world. In Indonesia, the greatest resistance to the uropathogen E. coli is resistant to ampicillin (91.9%), ciprofloxacin (83.7%) and cefixime (67.6%). Therefore it takes effort for...
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doaj-739a3ec347184eb3be0d38ee6d7c14232020-11-24T23:59:46ZengUniversitas Sultan Agung SemarangSains Medika2085-15452339-093X2017-04-0181202710.26532/sainsmed.v8i1.10021524Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli MultiresistenMaya Dian Rakhmawatie0Afiana Rohmani1Fariz Wafaul Ahyar2Bagian Farmakologi Fakultas Kedokteran Universitas Muhammadiyah SemarangBagian Farmakologi Fakultas Kedokteran Universitas Muhammadiyah SemarangBagian Farmakologi Fakultas Kedokteran Universitas Muhammadiyah SemarangBackground. The incidence of Multi Drug Resistant (MDR) in extraintestinal E. coli has become a global problem in the world. In Indonesia, the greatest resistance to the uropathogen E. coli is resistant to ampicillin (91.9%), ciprofloxacin (83.7%) and cefixime (67.6%). Therefore it takes effort for the treatment of MDR uropathogen E. coli, one of them are development of new antibiotics from herbal isolates of Garcinia mangostana L., α-mangosteen. This study examined the activity of α-mangosteen in vitro on the growth of MDR uropathogen E. coli. Methods. Treatment of uropathogen E. coli is performed in vitro, using α-mangosteen with a range of levels 14 - 450 µg/mL. The antibacterial activity of α-mangosteen is measured by determine at the growth or death of bacteria at each concentration using indirect methods, which is absorbance reading. Uropathogen E. coli that had been treated with various concentration of α-mangosteen incubated for 18-20 hours, then read an absorbance at wavelenght 625 nm using a spectrophotometer. Result. The Minimal Inhibitory Concentration (MIC) of α-mangosteen in this study was 450 µg/mL. Based on the linear regression (STATA 13.1) relationship between concentration of α-mangosteen and activity of growth inhibition of bacteria, obtained the F test value 0.0001 < 0.05, states that all concentrations of α-mangosteen simultaneously have a significant influence on the growth of uropathogen E. coli. Conclusion. MIC value is relatively large causing α-mangosteen activity against Gram-negative bacteria needs to be studied further. Potentially relevant activity in the clinic will occur if the value of in vitro MIC < 100 µg/mL. Likewise, the pharmaceutical industry prefers the development of antibiotics that have in vitro MIC values ≤ 2 µg/mL.http://jurnal.unissula.ac.id/index.php/sainsmedika/article/view/1002MDRantibioticGarcinia mangostana L. |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maya Dian Rakhmawatie Afiana Rohmani Fariz Wafaul Ahyar |
spellingShingle |
Maya Dian Rakhmawatie Afiana Rohmani Fariz Wafaul Ahyar Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten Sains Medika MDR antibiotic Garcinia mangostana L. |
author_facet |
Maya Dian Rakhmawatie Afiana Rohmani Fariz Wafaul Ahyar |
author_sort |
Maya Dian Rakhmawatie |
title |
Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten |
title_short |
Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten |
title_full |
Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten |
title_fullStr |
Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten |
title_full_unstemmed |
Efektivitas in vitro Alfa Mangostin Pada Pertumbuhan Bakteri Uropatogen Escherichia coli Multiresisten |
title_sort |
efektivitas in vitro alfa mangostin pada pertumbuhan bakteri uropatogen escherichia coli multiresisten |
publisher |
Universitas Sultan Agung Semarang |
series |
Sains Medika |
issn |
2085-1545 2339-093X |
publishDate |
2017-04-01 |
description |
Background. The incidence of Multi Drug Resistant (MDR) in extraintestinal E. coli has become a global problem in the world. In Indonesia, the greatest resistance to the uropathogen E. coli is resistant to ampicillin (91.9%), ciprofloxacin (83.7%) and cefixime (67.6%). Therefore it takes effort for the treatment of MDR uropathogen E. coli, one of them are development of new antibiotics from herbal isolates of Garcinia mangostana L., α-mangosteen. This study examined the activity of α-mangosteen in vitro on the growth of MDR uropathogen E. coli.
Methods. Treatment of uropathogen E. coli is performed in vitro, using α-mangosteen with a range of levels 14 - 450 µg/mL. The antibacterial activity of α-mangosteen is measured by determine at the growth or death of bacteria at each concentration using indirect methods, which is absorbance reading. Uropathogen E. coli that had been treated with various concentration of α-mangosteen incubated for 18-20 hours, then read an absorbance at wavelenght 625 nm using a spectrophotometer.
Result. The Minimal Inhibitory Concentration (MIC) of α-mangosteen in this study was 450 µg/mL. Based on the linear regression (STATA 13.1) relationship between concentration of α-mangosteen and activity of growth inhibition of bacteria, obtained the F test value 0.0001 < 0.05, states that all concentrations of α-mangosteen simultaneously have a significant influence on the growth of uropathogen E. coli.
Conclusion. MIC value is relatively large causing α-mangosteen activity against Gram-negative bacteria needs to be studied further. Potentially relevant activity in the clinic will occur if the value of in vitro MIC < 100 µg/mL. Likewise, the pharmaceutical industry prefers the development of antibiotics that have in vitro MIC values ≤ 2 µg/mL. |
topic |
MDR antibiotic Garcinia mangostana L. |
url |
http://jurnal.unissula.ac.id/index.php/sainsmedika/article/view/1002 |
work_keys_str_mv |
AT mayadianrakhmawatie efektivitasinvitroalfamangostinpadapertumbuhanbakteriuropatogenescherichiacolimultiresisten AT afianarohmani efektivitasinvitroalfamangostinpadapertumbuhanbakteriuropatogenescherichiacolimultiresisten AT farizwafaulahyar efektivitasinvitroalfamangostinpadapertumbuhanbakteriuropatogenescherichiacolimultiresisten |
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