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Reducing Staphylococcus aureus biofilm formation on stainless steel 316L using functionalized self-assembled monolayers
被引:35
作者:
Kruszewski, Kristen M.
[1
]
Nistico, Laura
[2
]
Longwell, Mark J.
[2
]
Hynes, Matthew J.
[3
]
Maurer, Joshua A.
[3
]
Hall-Stoodley, Luanne
[4
]
Gawalt, Ellen S.
[5
]
机构:
[1] Duquesne Univ, Dept Chem & Biochem, Pittsburgh, PA 15282 USA
[2] Allegheny Gen Hosp, Ctr Genom Sci, Allegheny Singer Res Inst, Pittsburgh, PA 15212 USA
[3] Washington Univ, Dept Chem, St Louis, MO 63130 USA
[4] Univ Southampton, Fac Med, Southampton Gen Hosp, Southampton Wellcome Trust Clin Res Facil NIHR Re, Southampton SO16 6YD, Hants, England
[5] Duquesne Univ, McGowan Inst Regenerat Med, Dept Chem & Biochem, Pittsburgh, PA 15282 USA
来源:
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
|
2013年
/
33卷
/
04期
关键词:
Stainless steel 316L;
Self-assembled monolayers;
Staphylococcus aureus;
Biofilms;
Gentamicin;
Oligoethylene glycol;
NATIVE-OXIDE SURFACE;
IN-VITRO;
BACTERIAL ADHESION;
HYDROPHOBIC SURFACES;
EPIDERMIDIS;
TITANIUM;
GOLD;
INFECTIONS;
VANCOMYCIN;
COATINGS;
D O I:
10.1016/j.msec.2013.01.023
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
Stainless steel 316L (SS316L) is a common material used in orthopedic implants. Bacterial colonization of the surface and subsequent biofilm development can lead to refractory infection of the implant. Since the greatest risk of infection occurs perioperatively, strategies that reduce bacterial adhesion during this time are important. As a strategy to limit bacterial adhesion and biofilm formation on SS316L, self-assembled monolayers (SAMs) were used to modify the SS316L surface. SAMs with long alkyl chains terminated with hydrophobic (-CH3) or hydrophilic (oligoethylene glycol) tail groups Were used to form coatings and in an orthogonal approach, SAMs were used to immobilize gentamicin or vancomycin on SS316L for the first time to form an "active" antimicrobial coating to inhibit early biofilm development. Modified SS316L surfaces were characterized using surface infrared spectroscopy, contact angles, MALDI-TOF mass spectrometry and atomic force microscopy. The ability of SAM-modified SS316L to retard biofilm development by Staphylococcus aureus was functionally tested using confocal scanning laser microscopy with COMSTAT image analysis, scanning electron microscopy and colony forming unit analysis. Neither hydrophobic nor hydrophilic SAMs reduced biofilm development. However, gentamicin-linked and vancomycin-linked SAMs significantly reduced S. aureus biofilm formation for up to 24 and 48 h, respectively. (c) 2013 Elsevier B.V. All rights reserved.
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页码:2059 / 2069
页数:11
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