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pubmed-article:17933534pubmed:dateCreated2007-11-6lld:pubmed
pubmed-article:17933534pubmed:abstractTextThe need for self-protecting polymer or alloy implants resistant to a broad spectrum of bacterial challenges led us to investigate covalent bonding of minocycline (MIN), a tetracycline derivative, to polystyrene beads and to titanium alloy foils by oligoethylene glycol spacers. 9-Hydrazino-acetyl-amido-MIN, and simpler glycylcycline derivatives, retained minimum inhibitory concentration (MIC) against Staphylococcus aureus comparable to MIN. However, PEG-glycyl-amido-MIN showed very low activity. Hence, we coupled 9-hydrazino-acetyl-amido-MIN to the aldehyde termini of oligoethylene glycol spacers bonded to polystyrene and titanium alloy surfaces to form acid-releasable hydrazone linkages. 9-Hydrazino-acetyl-amido-MIN was released from the monolayers more rapidly at pH 5.0 than at pH 7.4.lld:pubmed
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pubmed-article:17933534pubmed:authorpubmed-author:WickstromEric...lld:pubmed
pubmed-article:17933534pubmed:authorpubmed-author:ChenChang-poC...lld:pubmed
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pubmed-article:17933534pubmed:pagination6558-62lld:pubmed
pubmed-article:17933534pubmed:dateRevised2011-2-4lld:pubmed
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pubmed-article:17933534pubmed:year2007lld:pubmed
pubmed-article:17933534pubmed:articleTitleBactericidal activity of extended 9-glycyl-amido-minocyclines.lld:pubmed
pubmed-article:17933534pubmed:affiliationDepartment of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.lld:pubmed
pubmed-article:17933534pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17933534pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:17933534pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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