Ciprofloxacin-releasing bioabsorbable polymer is superior to titanium in preventing Staphylococcus epidermidis attachment and biofilm formation in vitro

被引:20
作者
Niemelä, SM
Ikäheimo, I
Koskela, M
Veiranto, M
Suokas, E
Törmälä, P
Waris, T
Ashammakhi, N [1 ]
Syrjälä, H
机构
[1] Oulu Univ Hosp, Dept Surg, Oulu, Finland
[2] Oulu Univ Hosp, Clin Microbiol Lab, Oulu, Finland
[3] Tampere Univ Technol, Inst Biomat, Tampere, Finland
[4] Linvatec Biomat Ltd, Tampere, Finland
[5] Oulu Univ Hosp, Dept Infect Control, Oulu, Finland
关键词
antibiotic; bioabsorbable; biofilm; ciprofloxacin; polylactide-co-glycolide;
D O I
10.1002/jbm.b.30414
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Antibiotic coating systems have been successfully used to prevent bacterial attachment and biofilm formation. Our purpose was to evaluate whether bioabsorbable polylactide-co-glycolide (PLGA) 80/20 on its own, and PLGA together with ciprofloxacin (PLGA + C) have any advantages over titanium in preventing Staphylococcus epidermidis attachment and biofilm formation in vitro. Cylindrical specimens of titanium, PLGA, and PLGA+C in triplicate were examined for S. epidermidis ATCC 35989 attachment and biofilm formation after incubation with a bacterial suspension of about 10(5) cfu/mL for 1, 3, 7, 14, and 21 days, using scanning electron microscopy. Growth inhibition properties of PLGA and PLGA+C cylinders were tested on agar plates. On days 1, 3, and 21, no bacterial attachment was seen in 19.5, 9.2, and 41.4% of the titanium specimens; in 18.4, 28.7, and 34.5% of the PLGA specimens; and in 57.5, 62.1, and 57.5% of the PLGA+C specimens, respectively. During the whole study period, no biofilm was observed on 74-93% of the titanium specimens, 58-78% of the PLGA specimens, and 93-100% of the PLGA+C specimens. PLGA+C showed clear bacterial growth inhibition on agar plates, while PLGA and titanium did not show any inhibition. PLGA+C bioabsorbable material was superior to titanium in preventing bacterial attachment and biofilm formation and may have clinical applicability, for example, in prevention of infection in trauma surgery or in the treatment of chronic osteomyelitis. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:8 / 14
页数:7
相关论文
共 24 条
[1]
An Yuehuei H., 1996, P19
[2]
Glycopeptide resistance in coagulase-negative staphylococci [J].
Biavasco, F ;
Vignaroli, C ;
Varaldo, PE .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (06) :403-417
[3]
Modulation of the production of cytokines in titanium-stimulated human peripheral blood monocytes by pharmacological agents - The role of cAMP-mediated signaling mechanisms [J].
Blaine, TA ;
Pollice, PF ;
Rosier, RN ;
Reynolds, PR ;
Puzas, JE ;
OKeefe, RJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1997, 79A (10) :1519-1528
[4]
Biomaterial-associated persistence of Streptococcus epidermidis in pericatheter macrophages [J].
Boelens, JJ ;
Dankert, J ;
Murk, JL ;
Weening, JJ ;
van der Poll, T ;
Dingemans, KP ;
Koole, L ;
Laman, JD ;
Zaat, SAJ .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (04) :1337-1349
[5]
Infection control - A problem for patient safety [J].
Burke, JP .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :651-656
[6]
ADHERENCE OF SLIME-PRODUCING STRAINS OF STAPHYLOCOCCUS-EPIDERMIDIS TO SMOOTH SURFACES [J].
CHRISTENSEN, GD ;
SIMPSON, WA ;
BISNO, AL ;
BEACHEY, EH .
INFECTION AND IMMUNITY, 1982, 37 (01) :318-326
[7]
CRAIG WA, 2002, INFEC DIS T, V28, P1
[8]
Linezolid compared with eperezolid, vancomycin, and gentamicin in an in vitro model of antimicrobial lock therapy for Staphylococcus epidermidis central venous catheter-related biofilm infections [J].
Curtin, J ;
Cormican, M ;
Fleming, G ;
Keelehan, J ;
Colleran, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (10) :3145-3148
[9]
Immunomodulatory effects of quinolones [J].
Dalhoff, A ;
Shalit, L .
LANCET INFECTIOUS DISEASES, 2003, 3 (06) :359-371
[10]
Device-associated infections: A macroproblem that starts with microadherence [J].
Darouiche, RO .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (09) :1567-1572