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dc.contributor.authorZhang, Xiao-Yanen_US
dc.contributor.authorLi, Zhe-Yuen_US
dc.contributor.authorUeno, Koseen_US
dc.contributor.authorMisawa, Hiroakien_US
dc.contributor.authorRen, Nan-Qien_US
dc.contributor.authorSun, Kaien_US
dc.date.accessioned2020-05-05T00:02:24Z-
dc.date.available2020-05-05T00:02:24Z-
dc.date.issued2020-02-01en_US
dc.identifier.urihttp://dx.doi.org/10.3390/mi11020207en_US
dc.identifier.urihttp://hdl.handle.net/11536/154203-
dc.description.abstractMinimum inhibition concentration (MIC) of antibiotic is an effective value to ascertain the agent and minimum dosage of inhibiting bacterial growth. However, current techniques to determine MIC are labor intensive and time-consuming, and require skilled operator and high initial concentration of bacteria. To simplify the operation and reduce the time of inhibition test, we developed a microfluidic system, containing a concentration generator and sub-micro-liter chambers, for rapid bacterial growth and inhibition test. To improve the mixing effect, a micropillar array in honeycomb-structure channels is designed, so the steady concentration gradient of amoxicillin can be generated. The flanged chambers are used to culture bacteria under the condition of continuous flow and the medium of chambers is refreshed constantly, which could supply the sufficient nutrient for bacteria growth and take away the metabolite. Based on the microfluidic platform, the bacterial growth with antibiotic inhibition on chip can be quantitatively measured and MIC can be obtained within six hours using low initial concentration of bacteria. Overall, this microfluidic platform has the potential to provide rapidness and effectiveness to screen bacteria and determine MIC of corresponding antibiotics in clinical therapies.en_US
dc.language.isoen_USen_US
dc.subjectminimum inhibition concentration (MIC)en_US
dc.subjectmicrofluidicen_US
dc.subjectbacteriaen_US
dc.subjectantibioticsen_US
dc.titleOn-chip MIC by Combining Concentration Gradient Generator and Flanged Chamber Arraysen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/mi11020207en_US
dc.identifier.journalMICROMACHINESen_US
dc.citation.volume11en_US
dc.citation.issue2en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.identifier.wosnumberWOS:000520181500096en_US
dc.citation.woscount0en_US
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