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Extraction of aminoglycoside antibiotics with reverse micelles

dc.contributor.authorHu, Ziyien_US
dc.contributor.authorGulari, Erdoganen_US
dc.date.accessioned2006-04-28T16:50:47Z
dc.date.available2006-04-28T16:50:47Z
dc.date.issued1996-01en_US
dc.identifier.citationHu, Ziyi; Gulari, Erdogan (1996)."Extraction of aminoglycoside antibiotics with reverse micelles." Journal of Chemical Technology AND Biotechnology 65(1): 45-48. <http://hdl.handle.net/2027.42/38295>en_US
dc.identifier.issn0268-2575en_US
dc.identifier.issn1097-4660en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38295
dc.description.abstractThe reverse micelle system of sodium di-2-ethylhexyl phosphate was used to extract aminoglycoside antibiotics, neomycin and gentamicin. The aminoglycosides can be efficiently extracted into a reverse micelle solution, and the antibiotics extracted into the micelle phase can readily be recovered back to a divalent cation aqueous solution, such as Ca 2+ . The transfer efficiency, % E , is heavily dependent on pH and salt concentration in the aqueous feed solution. % E decreases drastically with pH in the pH range 8·5–11, and declines with increasing (NH 4 ) 2 SO 4 concentration. A simple transfer mechanism was proposed which suggests that the antibiotic molecules were extracted into the inner water cores of reverse micelles through attractive electrostatic interaction during forward transfer. In backward transfer, the antibiotics loaded in the micelle phase are released back to an aqueous phase through breaking up of the reverse micelles by using divalent cation solutions. The model is supported by the results of dynamic light scattering and infra-red spectroscopy study.en_US
dc.format.extent342201 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherBiochemistry and Biotechnologyen_US
dc.titleExtraction of aminoglycoside antibiotics with reverse micellesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemical Engineering, The University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Chemical Engineering, The University of Michigan, Ann Arbor, Michigan, USA ; Department of Chemical Engineering, The University of Michigan, Ann Arbor, Michigan, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38295/1/390_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-4660(199601)65:1<45::AID-JCTB390>3.0.CO;2-9en_US
dc.identifier.sourceJournal of Chemical Technology AND Biotechnologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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