Synthesis, characterization and in vitro activity of a surface-attached antimicrobial cationic peptide
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Chen, Renxun
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Univ New S Wales, Sch Chem, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Chen, Renxun
[1
]
Cole, Nerida
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Eye Res Inst, Sydney, NSW 2052, Australia
Vis CRC, Sydney, NSW 2052, Australia
Univ New S Wales, Sch Optometry & Vis Sci, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Cole, Nerida
[2
,3
,4
]
Willcox, Mark D. P.
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Eye Res Inst, Sydney, NSW 2052, Australia
Vis CRC, Sydney, NSW 2052, Australia
Univ New S Wales, Sch Optometry & Vis Sci, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Willcox, Mark D. P.
[2
,3
,4
]
Park, Josephine
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Univ New S Wales, Sch Chem, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Park, Josephine
[1
]
Rasul, Riaz
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Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Univ New S Wales, Sch Optometry & Vis Sci, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Rasul, Riaz
[1
,4
]
Carter, Elizabeth
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Univ Sydney, Sch Chem, Sydney, NSW 2006, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Carter, Elizabeth
[5
]
Kumar, Naresh
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Univ New S Wales, Sch Chem, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem, Sydney, NSW 2052, Australia
Kumar, Naresh
[1
]
机构:
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[2] Eye Res Inst, Sydney, NSW 2052, Australia
[3] Vis CRC, Sydney, NSW 2052, Australia
[4] Univ New S Wales, Sch Optometry & Vis Sci, Sydney, NSW 2052, Australia
[5] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
Infection associated with implanted biomaterials is common and costly and such infections are extremely resistant to antibiotics and host defenses. Consequently, there is a need to develop surfaces which resist bacterial adhesion and colonization. The broad spectrum synthetic cationic peptide melimine has been covalently linked to a surface via two azide linkers, 4-azidobenzoic acid (ABA) or 4-fluoro-3-nitrophenyl azide (FNA), and the resulting surfaces characterized by X-ray photoelectron spectroscopy and contact angle measurements. The quantity of bound peptide was estimated by a modified Bradford assay. The antimicrobial efficacy of the two melimine-modified surfaces against Pseudomonas aeruginosa and Staphylococcus aureus was compared by scanning electron microscopy (SEM) and fluorescence microscopy. Attachment of melimine via ABA gave an approximately 4-fold greater quantity of melimine bound to the surface than attachment via FNA. Surfaces melimine-modified by either attachment strategy showed significantly reduced bacterial adhesion for both strains of bacteria. P. aeruginosa exposed to ABA-melimine and FNA-melimine surfaces showed marked changes in cell morphology when observed by SEM and a reduction of approximately 15-fold (p < 0.001) in the numbers of adherent bacteria compared to controls. For the ABA-melimine surface there was a 33% increase in cells showing damaged membranes (p = 0.0016) while for FNA-melimine there was no significant difference. For S. aureus there were reductions in bacterial adhesion of approximately 40-fold (p < 0.0001) and 5-fold (p = 0.008) for surfaces modified with melimine via ABA or FNA, respectively. There was an increase in cells showing damaged membranes on ABA-melimine surfaces of approximately 87% (p = 0.001) compared to controls, while for FNA-melimine there was no significant difference observed. The data presented in this study show that melimine has excellent potential for development as a broad spectrum antimicrobial coating for biomaterial surfaces. Further, it was observed that the efficacy of antimicrobial activity is related to the method of attachment.
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页码:517 / 524
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