In vivo efficacy of a silicone-cationic steroid antimicrobial coating to prevent implant-related infection

被引:49
作者
Williams, Dustin L. [1 ,2 ,3 ]
Haymond, Bryan S. [1 ,3 ]
Beck, James P. [1 ,3 ]
Savage, Paul B. [4 ]
Chaudhary, Vinod [4 ]
Epperson, Richard T. [1 ,3 ]
Kawaguchi, Brooke [1 ,3 ]
Bloebaum, Roy D. [1 ,2 ,3 ]
机构
[1] George E Wahlen Dept Vet Affairs, Med Ctr, Salt Lake City, UT 84148 USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Orthopaed, Salt Lake City, UT USA
[4] Brigham Young Univ, Dept Chem & Biochem, Salt Lake City, UT 84602 USA
关键词
Active release coating; Biofilm; Initial inocula; Animal model; Infection; CONTROLLED-RELEASE; BIOFILM FORMATION; RABBIT MODEL; OSTEOMYELITIS; COLONIZATION; RESISTANCE; DEVICES; IMPACT; CELLS; ANTIBIOTICS;
D O I
10.1016/j.biomaterials.2012.08.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Active release antimicrobial coatings for medical devices have been developed to prevent and treat biofilm implant-related infections. To date, only a handful of coatings have been put into clinical use, with limited success. In this study, a novel antimicrobial compound was incorporated into a silicone (polydimethylsiloxane or PDMS) polymer to develop a novel active release coating that addressed several limitations of current device coatings. The efficacy of this coating was optimized using an in vitro flow cells system, then translated to an animal model of a simulated Type IIIB open fracture wherein well-established biofilms were used as initial inocula. Results indicated that the novel coating was able to prevent infection in 100% (9/9) of animals that were treated with biofilms and the novel coating (treatment group). In contrast, 100% (9/9) of animals that were inoculated with biofilms and not treated with the coating (positive control), did develop infection. Nine animals were used as negative controls, i.e., those that were not treated with biofilms, and showed a rate of infection of 11% (1/9). Eight animals were treated with the novel coating only to determine its effect on host tissue. Results indicated that the novel active release coating may have significant promise for future application to prevent biofilm implant-related infections in patients. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8641 / 8656
页数:16
相关论文
共 67 条
[1]   Comparison of Oligon catheters and chlorhexidine-impregnated sponges with standard multilumen central venous catheters for prevention of associated colonization and infections in intensive care unit patients: A multicenter, randomized, controlled study [J].
Arvaniti, Kostoula ;
Lathyris, Dimitrios ;
Clouva-Molyvdas, Phyllis ;
Haidich, Anna-Bettina ;
Mouloudi, Eleni ;
Synnefaki, Eleni ;
Koulourida, Vasiliki ;
Georgopoulos, Dimitrios ;
Gerogianni, Nikoleta ;
Nakos, Georgios ;
Matamis, Dimitrios .
CRITICAL CARE MEDICINE, 2012, 40 (02) :420-429
[2]   Relationship between bone ingrowth, mineral apposition rate, and osteoblast activity [J].
Bloebaum, R. D. ;
Willie, B. M. ;
Mitchell, B. S. ;
Hofmann, A. A. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 81A (02) :505-514
[3]   Hydrogel/silver ion-coated urinary catheter reduces nosocomial urinary tract infection rates in intensive care unit patients: A multicenter study [J].
Bologna, RA ;
Tu, LM ;
Polansky, M ;
Fraimow, HD ;
Gordon, DA ;
Whitmore, KE .
UROLOGY, 1999, 54 (06) :982-987
[4]   Treatment of osteomyelitis in rats by injection of degradable polymer releasing gentamicin [J].
Brin, Yaron S. ;
Golenser, Jacob ;
Mizrahi, Boaz ;
Maoz, Guy ;
Domb, Abraham J. ;
Peddada, Shyamal ;
Tuvia, Shmuel ;
Nyska, Abraham ;
Nyska, Meir .
JOURNAL OF CONTROLLED RELEASE, 2008, 131 (02) :121-127
[5]   Resistance of the antibacterial agent ceragenin CSA-13 to inactivation by DNA or F-actin and its activity in cystic fibrosis sputum [J].
Bucki, Robert ;
Sostarecz, Audra Goach ;
Byfield, Fitzroy J. ;
Savage, Paul B. ;
Janmey, Paul A. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2007, 60 (03) :535-545
[6]   AN INVIVO MODEL TO STUDY THE PATHOBIOLOGY OF INFECTIOUS BIOFILMS ON BIOMATERIAL SURFACES [J].
BURET, A ;
WARD, KH ;
OLSON, ME ;
COSTERTON, JW .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1991, 25 (07) :865-874
[7]  
Ceri H, 2005, BIOFILMS, INFECTION, AND ANTIMICROBIAL THERAPY, P257, DOI 10.1201/9781420028232.ch13
[8]   Do antibacterial-coated sutures reduce wound infection in head and neck cancer reconstruction? [J].
Chen, S. Y. ;
Chen, T. M. ;
Dai, N. T. ;
Fu, J. P. ;
Chang, S. C. ;
Deng, S. C. ;
Chen, S. G. .
EJSO, 2011, 37 (04) :300-304
[9]   Antimicrobial activities of ceragenins against clinical isolates of resistant Staphylococcus aureus [J].
Chin, Judy N. ;
Rybak, Michael J. ;
Cheung, Chrissy M. ;
Savage, Paul B. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (04) :1268-1273
[10]   Daptomycin and Rifampin Alone and in Combination Prevent Vascular Graft Biofilm Formation and Emergence of Antibiotic Resistance in a Subcutaneous Rat Pouch Model of Staphylococcal Infection [J].
Cirioni, O. ;
Mocchegiani, F. ;
Ghiselli, R. ;
Silvestri, C. ;
Gabrielli, E. ;
Marchionni, E. ;
Orlando, F. ;
Nicolini, D. ;
Risaliti, A. ;
Giacometti, A. .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2010, 40 (06) :817-822