Bacterial adherence to ofloxacin-blended polylactone-coated self-reinforced L-lactic acid polymer urological stents

被引:16
作者
Multanen, M
Talja, M
Hallanvuo, S
Siitonen, A
Välimaa, T
Tammela, TLJ
Seppälä, J
Törmälä, P
机构
[1] Paijat Hame Cent Hosp, Dept Surg, Div Urol, Lahti 15850, Finland
[2] Natl Publ Hlth Inst, Lab Enter Pathogens, Helsinki, Finland
[3] Tampere Univ Technol, Inst Biomat, FIN-33101 Tampere, Finland
[4] Tampere Univ Hosp, Div Urol, Tampere, Finland
[5] Helsinki Univ Technol, FIN-02150 Espoo, Finland
关键词
bioresorbable material; urology; infection; stents; antibacterial coating;
D O I
10.1046/j.1464-410x.2000.00964.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To determine whether ofloxacin coating has any effect on bacterial adherence to bioresorbable self-reinforced l-lactic acid polymer (SR-PLLA) urological stents. Materials and methods SR-PLLA stents were coated with epsilon -caprolactone/l-lactide copolymer blended with ofloxacin at three different concentrations of ofloxacin (0.5, 2 and 5% w/w). The adherence of five bacterial strains (Pseudomonas aeruginosa, Enterococcus faecalis, Proteus mirabilis and two strains of Escherichia coli) to the coated SR-PLLA stents was analysed. Uncoated stent pieces were used as controls. The effect of ofloxacin coating on bacterial growth in the microenvironment of the stent pieces was also analysed. Results Ofloxacin coating prevented bacterial adherence to SR-PLLA stent material; this effect correlated significantly with the ofloxacin concentration of the caprolactone coating. Ofloxacin coating reduced the amount of bacteria in the microenvironment of the stent, but because of natural resistance, ofloxacin coating had little effect on E. faecalis. Conclusion Except for E. faecalis, ofloxacin coating may reduce stent-associated infections. However, further studies are needed to confirm its biocompatibility and efficacy in clinical use.
引用
收藏
页码:966 / 969
页数:4
相关论文
共 16 条
[1]   TESTING THE SUSCEPTIBILITY OF BACTERIA IN BIOFILMS TO ANTIBACTERIAL AGENTS [J].
ANWAR, H ;
DASGUPTA, MK ;
COSTERTON, JW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (11) :2043-2046
[2]   Bacterial adhesion and biofilm formation on various double-J stents in vivo and in vitro [J].
Cormio, L ;
VuopioVarkila, J ;
Siitonen, A ;
Talja, M ;
Ruutu, M .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 1996, 30 (01) :19-24
[3]   Immersion in antibiotic solution prevents bacterial adhesion onto biodegradable prostatic stents [J].
Cormio, L ;
LaForgia, P ;
Siitonen, A ;
Ruutu, M ;
Tormala, P ;
Talja, M .
BRITISH JOURNAL OF UROLOGY, 1997, 79 (03) :409-413
[4]   BACTERIAL BIOFILMS IN NATURE AND DISEASE [J].
COSTERTON, JW ;
CHENG, KJ ;
GEESEY, GG ;
LADD, TI ;
NICKEL, JC ;
DASGUPTA, M ;
MARRIE, TJ .
ANNUAL REVIEW OF MICROBIOLOGY, 1987, 41 :435-464
[5]   Biomaterials used in urology: Current issues of biocompatibility, infection, and encrustation [J].
Denstedt, JD ;
Wollin, TA ;
Reid, G .
JOURNAL OF ENDOUROLOGY, 1998, 12 (06) :493-500
[6]  
Emil S. E., 1967, U.S. Patent, Patent No. [3,297,033, 3297033]
[7]   Assessment of encrustation behaviour on urinary tract biomaterials [J].
Gorman, SP ;
Tunney, MM .
JOURNAL OF BIOMATERIALS APPLICATIONS, 1997, 12 (02) :136-166
[8]  
ISOTALO T, 2000, IN PRESS J UROL
[9]  
KULKARNI RK, 1966, ARCH SURG-CHICAGO, V93, P839
[10]  
LIEDBERG H, 1989, THESIS STOCKHOLM