Linked Life Data

21391641

Source:http://linkedlifedata.com/resource/pubmed/id/21391641

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pubmed-article:21391641pubmed:issue7lld:pubmed
pubmed-article:21391641pubmed:dateCreated2011-3-30lld:pubmed
pubmed-article:21391641pubmed:abstractTextA new strategy for preparing antimicrobial surfaces by a simple dip-coating procedure is reported. Amphiphilic polycations with different mole ratios of monomers containing dodecyl quaternary ammonium, methoxyethyl, and catechol groups were synthesized by free-radical polymerization. The polymer coatings were prepared by immersing glass slides into a polymer solution and subsequent drying and heating. The quaternary ammonium side chains endow the coatings with potent antibacterial activity, the methoxyethyl side chains enable tuning the hydrophobic/hydrophilic balance, and the catachol groups promote immobilization of the polymers into films. The polymer-coated surfaces displayed bactericidal activity against Escherichia coli and Staphylococcus aureus in a dynamic contact assay and prevented the accumulation of viable E. coli, S. aureus, and Acinetobacter baumannii for up to 96 h. Atomic force microscopy (AFM) images of coating surfaces indicated that the surfaces exhibit virtually the same smoothness for all polymers except the most hydrophobic. The hydrophobic polymer without methoxyethyl side chains showed clear structuring into polymer domains, causing high surface roughness. Sum-frequency generation (SFG) vibrational spectroscopy characterization of the surface structures demonstrated that the dodecyl chains are predominantly localized at the surface-air interface of the coatings. SFG also showed that the phenyl groups of the catechols are oriented on the substrate surface. These results support our hypothesis that the adhesive or cross-linking functionality of catechol groups discourages polymer leaching, allowing the tuning of the amphiphilic balance by incorporating hydrophilic components into the polymer chains to gain potent biocidal activity.lld:pubmed
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pubmed-article:21391641pubmed:authorpubmed-author:XiChuanwuClld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:HanHuaHlld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:ChenZhanZlld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:KamigaitoMasa...lld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:KurodaKenichi...lld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:MizutaniMasat...lld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:WuJianfengJlld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:JiangXiaoming...lld:pubmed
pubmed-article:21391641pubmed:authorpubmed-author:AveryChristop...lld:pubmed
pubmed-article:21391641pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21391641pubmed:day5lld:pubmed
pubmed-article:21391641pubmed:volume27lld:pubmed
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pubmed-article:21391641pubmed:pagination4010-9lld:pubmed
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pubmed-article:21391641pubmed:year2011lld:pubmed
pubmed-article:21391641pubmed:articleTitleImmobilization of amphiphilic polycations by catechol functionality for antimicrobial coatings.lld:pubmed
pubmed-article:21391641pubmed:affiliationDepartment of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, Michigan 48109, United States.lld:pubmed
pubmed-article:21391641pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21391641pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:21391641pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:21391641pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed