Antimicrobial Surfaces Using Covalently Bound Polyallylamine

被引:46
作者
Iarikov, Dmitri D. [1 ]
Kargar, Mehdi [2 ]
Sahari, Ali [3 ]
Russel, Lauren [1 ]
Gause, Katelyn T. [1 ]
Behkam, Bahareh [2 ,3 ]
Ducker, William A. [1 ]
机构
[1] Virginia Tech, Dept Chem Engn, Blacksburg, VA 24061 USA
[2] Virginia Tech, Dept Mech Engn, Blacksburg, VA 24061 USA
[3] Virginia Tech, Sch Biomed Engn & Sci, Blacksburg, VA 24061 USA
关键词
ANTIBACTERIAL; PEPTIDES;
D O I
10.1021/bm401440h
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the antimicrobial properties of the cationic polymer polyallylamine (PA) when covalently bonded to glass. The objective was to obtain a robust attachment, yet still allow extension of the polymer chain into solution to enable interaction with the bacteria. The PA film displayed strong antimicrobial activity against Staphylococcus epidermidis, Staphylococcus aureus, and Pseudomonas aeruginosa, which includes both Gram-positive and Gram-negative bacteria. Glass surfaces were prepared by a straightforward two-step procedure of first functionalizing with epoxide groups using 3-glycidoxypropyltrimethoxy silane (GOPTS) and then exposing to PA so that the PA could bind via reaction of a fraction of its amine groups. The surfaces were characterized using X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy to verify the presence of the polymer on the surface, zeta potential measurements to estimate the surface charge of the films, and atomic force microscopy to determine the extension of the polymer chains into solution. Antimicrobial properties of these coatings were evaluated by spraying aqueous suspensions of bacteria on the functionalized glass slides, incubating them under agar, and counting the number of surviving cell colonies.
引用
收藏
页码:169 / 176
页数:8
相关论文
共 44 条
[1]   Surfaces modified with nanometer-thick silver-impregnated polymeric films that kill bacteria but support growth of mammalian cells [J].
Agarwal, Ankit ;
Weis, Tahlia L. ;
Schurr, Michael J. ;
Faith, Nancy G. ;
Czuprynski, Charles J. ;
McAnulty, Jonathan F. ;
Murphy, Christopher J. ;
Abbott, Nicholas L. .
BIOMATERIALS, 2010, 31 (04) :680-690
[2]   INHIBITION OF STAPHYLOCOCCI BY VANCOMYCIN ABSORBED ON TRIIDODECYLMETHYL AMMONIUM CHLORIDE-COATED INTRAVENOUS CATHETER [J].
BOWERSOCK, TL ;
WOODYARD, L ;
HAMILTON, AJ ;
DEFORD, JA .
JOURNAL OF CONTROLLED RELEASE, 1994, 31 (03) :237-243
[3]   Medical Biofilms [J].
Bryers, James D. .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (01) :1-18
[4]   Detachment of a single polyelectrolyte chain adsorbed on a charged surface [J].
Chatellier, X ;
Senden, TJ ;
Joanny, JF ;
di Meglio, JM .
EUROPHYSICS LETTERS, 1998, 41 (03) :303-308
[5]   Disinfection and the prevention of infectious disease [J].
Cozad, A ;
Jones, RD .
AMERICAN JOURNAL OF INFECTION CONTROL, 2003, 31 (04) :243-254
[6]   Infections in nonleukopenic compromised hosts (diabetes mellitus, SLE, steroids, and asplenia) in critical care [J].
Cunha, BA .
CRITICAL CARE CLINICS, 1998, 14 (02) :263-+
[7]  
Cunliffe D, 1999, APPL ENVIRON MICROB, V65, P4995
[8]   Tertiary structure of Staphylococcus aureus cell wall murein [J].
Dmitriev, BA ;
Holst, O ;
Rietschel, ET ;
Ehlers, S .
JOURNAL OF BACTERIOLOGY, 2004, 186 (21) :7141-7148
[9]   MEASURING THE ZETA (ELECTROKINETIC) POTENTIAL OF REVERSE-OSMOSIS MEMBRANES BY A STREAMING POTENTIAL ANALYZER [J].
ELIMELECH, M ;
CHEN, WH ;
WAYPA, JJ .
DESALINATION, 1994, 95 (03) :269-286
[10]   Vancomycin heteroresistance and biofilm formation in Staphylococcus epidermidis from food [J].
Gazzola, Shona ;
Cocconcelli, Pier Sandro .
MICROBIOLOGY-SGM, 2008, 154 :3224-3231