New PMMA-based composites for preparing spacer devices in prosthetic infections

被引:18
作者
Giavaresi, Gianluca [1 ]
Minelli, Elisa Bertazzoni [2 ]
Sartori, Maria [3 ]
Benini, Anna [2 ]
Parrilli, Annapaola [3 ]
Maltarello, Maria Cristina [4 ]
Salamanna, Francesca [3 ]
Torricelli, Paola [1 ]
Giardino, Roberto [3 ]
Fini, Milena [1 ]
机构
[1] Rizzoli Orthopaed Inst IRCCS, Lab Preclin & Surg Studies, I-40136 Bologna, Italy
[2] Univ Verona, Policlin GB Rossi, Pharmacol Sect, Dept Publ Hlth & Community Med, I-37134 Verona, Italy
[3] Rizzoli Orthopaed Inst IRCCS, Lab Biocompatibil Innovat Technol & Adv Therapies, I-40136 Bologna, Italy
[4] Rizzoli Orthopaed Inst IRCCS, Lab Musculoskeletal Cell Biol, I-40136 Bologna, Italy
关键词
LOADED BONE CEMENTS; TRICALCIUM PHOSPHATE; SURFACE-ROUGHNESS; HIP SPACERS; GENTAMICIN; VANCOMYCIN; POLYMETHYLMETHACRYLATE; RELEASE; MANAGEMENT; RESPONSES;
D O I
10.1007/s10856-012-4585-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Even though the systemic antibiotic therapy is usually applied after prosthetic infections surgical treatments, it is unable to reach the infection site in sufficient concentrations to eradicate bacteria. Delivering antibiotics locally with the use of custom made device (spacer or nail coating) might eradicate or reduce the infection and the risk of recolonization, providing a very high concentration of antibiotic. PMMA-based (Mendec Spine(A (R))) composites with BaSO4 were enriched with beta-tricalcium phosphate (Porosectan-TCP) or only a slightly higher BaSO4 concentration (Porosectan-BaSO4) to obtain higher porosity. The aim of the study was to evaluate: (i) drug absorption capability and drug release kinetics in vitro soaking them with a combined solution of gentamicin and vancomycin, (ii) their in vitro and in vivo biocompatibility, and finally, (iii) they were tested preliminarily in an experimental model of bone infection. The simultaneous presence of beta-TCP and BaSO4 resulted in the formation of a texture of interconnecting channels with different diameters, from a few microns to several hundred microns, which totally filled the material. The porosity, determined by microcomputed tomography, was significantly higher in both tested plain composites (Porosectan-TCP: +17.3%; Porosectan-BaSO4: +7.5%) in comparison to control composite material (Mendec Spine(A (R))). The kinetics of antibiotic release from composites was rapid and complete, producing high drug concentrations for a short period of time. Both composites showed a good level of biocompatibility. The osteomyelitic model confirmed that both composites, soaked in antibiotic solution, were able to cure bone infection. These composites could be useful for preparing devices for prosthetic joint infections treatment also allowing the use of antibiotics solution at required concentrations.
引用
收藏
页码:1247 / 1257
页数:11
相关论文
共 42 条
[1]  
An YHH, 1998, ANIMAL MODELS IN ORTHOPAEDIC RESEARCH, P443
[2]   Elution of gentamicin and vancomycin from polymethylmethacrylate beads and hip spacers in vivo [J].
Anagnostakos, Konstantinos ;
Wilmes, Philippe ;
Schmitt, Eduard ;
Kelm, Jens .
ACTA ORTHOPAEDICA, 2009, 80 (02) :193-197
[3]   A comparative study of biphasic calcium phosphate ceramics for human mesenchymal stem-cell-induced bone formation [J].
Arinzeh, TL ;
Tran, T ;
Mcalary, J ;
Daculsi, G .
BIOMATERIALS, 2005, 26 (17) :3631-3638
[4]  
*CLIN LAB STAND I, 2009, M100S19 CLIN LAB STA
[5]   The infected total knee - Management options [J].
Cuckler, JM .
JOURNAL OF ARTHROPLASTY, 2005, 20 (04) :33-36
[6]   Antibiotic-impregnated cement spacers for the treatment of infection associated with total hip or knee arthroplasty [J].
Cui, Quanjun ;
Mihalko, William M. ;
Shields, John S. ;
Ries, Michael ;
Saleh, Khaled J. .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2007, 89A (04) :871-882
[7]  
Deb S, 2009, BIOMEDICAL COMPOSITES, P210
[8]  
Edin ML, 1996, CLIN ORTHOP RELAT R, P245
[9]   Comparable efficacies of the antimicrobial peptide human lactoferrin 1-11 and gentamicin in a chronic methicillin-resistant Staphylococcus aureus osteomyelitis model [J].
Faber, C ;
Stallmann, HP ;
Lyaruu, DM ;
Joosten, U ;
von Eiff, C ;
Amerongen, AV ;
Wuisman, PIJM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (06) :2438-2444
[10]   A bone substitute composed of polymethylmethacrylate and α-tricalcium phosphate:: results in terms of osteoblast function and bone tissue formation [J].
Fini, M ;
Giavaresi, G ;
Aldini, NN ;
Torricelli, P ;
Botter, R ;
Beruto, D ;
Giardino, R .
BIOMATERIALS, 2002, 23 (23) :4523-4531