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dc.contributor.authorJong Wook Hong-
dc.date.accessioned2017-03-08T04:47:23Z-
dc.date.available2017-03-08T04:47:23Z-
dc.date.issued2015-06-
dc.identifier.citationBIOTECHNOLOGY JOURNAL, v. 10, NO 11, Page. 1783-1791en_US
dc.identifier.issn1860-6768-
dc.identifier.issn1860-7314-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/biot.201500037/abstract;jsessionid=7BFCAEED286FF9ED558870A727BFB77E.f04t02-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/25938-
dc.description.abstractCurrent existing assay systems for evaluating antimicrobial activity suffer from several limitations including excess reagent consumption and inaccurate concentration gradient preparation. Recently, microfluidic systems have been developed to provide miniaturized platforms for antimicrobial susceptibility assays. However, some of current microfluidic based assays require continuous flows of reagents or elaborate preparation steps during concentration preparation. In this study, we introduce a novel microfluidic chip based growth phenotype assay that automatically generates a logarithmic concentration gradient and allows observing the growth of pathogenic bacteria under different concentrations of antibiotics in nanoliter batch culture reactors. We chose pathogen bacterium Pseudomonas aeruginosa as a model strain and evaluated the inhibitory effects of gentamicin and ciprofloxacin. We determined the EC50 values and confirmed the validity of the present system by comparing the EC50 values obtained through conventional test tube method. We demonstrated that the EC50 values acquired from present assay are comparable to those obtained from conventional test tube cultures. The potential application of present assay system for investigating combinatorial effects of antibiotics on multidrug resistant pathogenic bacteria is discussed and it can be further used for systematic evaluation of antifungal or antiviral agents.en_US
dc.description.sponsorshipThis research was supported by the National Institutes of Health (NIH Grant R01 008392) and the National Science Foundation (NSF CBET Grant 1063536) of the USA. We also acknowledge partial support from the USDA Nano-technology Program (CSREES 2008-01437) and the Global Frontier Project Grant (NRF-MiAXA002-20010031419) of the National Science Foundation funded by the Ministry of Education, Science and Technology of Korea. We thank Dr. Sachin Jambovane for helpful discussion of data analysis.en_US
dc.language.isoenen_US
dc.publisherWILEY-V C H VERLAG GMBHen_US
dc.subjectAntibiotic susceptibilityen_US
dc.subjectGrowth phenotype assayen_US
dc.subjectHalf maximal effective concentration (EC50)en_US
dc.subjectLogarithmic concentration gradienten_US
dc.subjectMicrofluidicsen_US
dc.titleDetermination of antibiotic EC50 using a zero-flow microfluidic chip based growth phenotype assayen_US
dc.typeArticleen_US
dc.relation.no11-
dc.relation.volume10-
dc.identifier.doi10.1002/biot.201500037-
dc.relation.page1783-1791-
dc.relation.journalBIOTECHNOLOGY JOURNAL-
dc.contributor.googleauthorDai, Jing-
dc.contributor.googleauthorSuh, Sang-Jin-
dc.contributor.googleauthorHamon, Morgan-
dc.contributor.googleauthorHong, Jong Wook-
dc.relation.code2015008337-
dc.sector.campusS-
dc.sector.daehakGRADUATE SCHOOL[S]-
dc.sector.departmentDEPARTMENT OF BIONANOTECHNOLOGY-
dc.identifier.pidjwh-
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GRADUATE SCHOOL[S](대학원) > BIONANOTECHNOLOGY(바이오나노학과) > Articles
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