Inhibition of implant-associated infections via nitric oxide

被引:130
作者
Nablo, BJ
Prichard, HL
Butler, RD
Klitzman, B
Schoenfisch, MH [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[2] Duke Univ, Med Ctr, Kenan Plast Surg Res Labs, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Biomed Engn, Durham, NC 27710 USA
关键词
Staphylococcus aureus; implant infection; sol-gel; nitric oxide; in vivo;
D O I
10.1016/j.biomaterials.2005.05.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The in vivo antibacterial activity of nitric oxide (NO)-releasing xerogel coatings was evaluated against an aggressive subcutaneous Staphylococcus aureus infection in a rat model. The NO-releasing implants were created by coating a medical-grade silicone elastomer with a sol-gel-derived (xerogel) film capable of storing NO. Four of the bare or xerogel-coated silicone materials were subcutaneously implanted into male rats. Ten rats were administered 10 mu l of a 10(8) cfu ml(-1) S. aureus colony directly into the subcutaneous pocket with the implant prior to wound closure. Infection was quantitatively and qualitatively evaluated after 8d of implantation with microbiological and histological methods, respectively. A 82% reduction in the number of infected implants was achieved with the NO-releasing coating. Histology revealed that the capsule formation around infected bare silicone rubber controls was immunoactive and that a biofilm may have formed. Capsule formation in response to NO-releasing implants had greater vascularity in comparison with uninoculated or untreated controls. These results suggest that NO-releasing coatings may dramatically reduce the incidence of biomaterial-associated infection. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6984 / 6990
页数:7
相关论文
共 15 条
[1]   Prevention of sepsis in total joint arthroplasty [J].
An, YH ;
Friedman, RJ .
JOURNAL OF HOSPITAL INFECTION, 1996, 33 (02) :93-108
[2]   Natural pathogens of laboratory mice, rats, and rabbits and their effects on research [J].
Baker, DG .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (02) :231-+
[3]   NEW NITRIC OXIDE-RELEASING ZWITTERIONS DERIVED FROM POLYAMINES [J].
HRABIE, JA ;
KLOSE, JR ;
WINK, DA ;
KEEFER, LK .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (06) :1472-1476
[4]   PEROXYNITRITE FORMATION FROM MACROPHAGE-DERIVED NITRIC-OXIDE [J].
ISCHIROPOULOS, H ;
ZHU, L ;
BECKMAN, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 298 (02) :446-451
[5]  
Jarvis WR, 1996, INFECT CONT HOSP EP, V17, P552
[6]   Preparation of nitric oxide (NO)-releasing sol-gels for biomaterial applications [J].
Marxer, SM ;
Rothrock, AR ;
Nablo, BJ ;
Robbins, ME ;
Schoenfisch, MH .
CHEMISTRY OF MATERIALS, 2003, 15 (22) :4193-4199
[7]   Nitric oxide-releasing sol-gels as antibacterial coatings for orthopedic implants [J].
Nablo, BJ ;
Rothrock, AR ;
Schoenfisch, MH .
BIOMATERIALS, 2005, 26 (08) :917-924
[8]   Poly(vinyl chloride)-coated sol-gels for studying the effects of nitric oxide release on bacterial adhesion [J].
Nablo, BJ ;
Schoenfisch, MH .
BIOMACROMOLECULES, 2004, 5 (05) :2034-2041
[9]   Antibacterial properties of nitric oxide-releasing sol-gels [J].
Nablo, BJ ;
Schoenfisch, MH .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 67A (04) :1276-1283
[10]   Sol-gel derived nitric-oxide releasing materials that reduce bacterial adhesion [J].
Nablo, BJ ;
Chen, TY ;
Schoenfisch, MH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (39) :9712-9713