Covalent Coating of Hydroxyapatite by Keratin Stabilizes Gentamicin Release

被引:27
作者
Belcarz, Anna [1 ]
Ginalska, Grazyna [1 ]
Zalewska, Justyna [1 ]
Rzeski, Wojciech [2 ]
Slosarczyk, Anna [3 ]
Kowalczulk, Dorota [4 ]
Godlewski, Piotr [5 ]
Niedzwiadek, Justyna [6 ]
机构
[1] Med Univ Lublin, Dept Biochem, PL-20093 Lublin, Poland
[2] Inst Agr Med, Dept Toxicol, PL-20950 Lublin, Poland
[3] AGH Univ Sci & Technol, Fac Mat Sci & Ceram, PL-30059 Krakow, Poland
[4] Med Univ Lublin, Dept Med Chem, PL-20090 Lublin, Poland
[5] Med Univ Lublin, Dept Orthoped & Traumatol, PL-20954 Lublin, Poland
[6] Med Univ Lublin, Dept Med Microbiol, PL-20093 Lublin, Poland
关键词
hydroxyapatite; porosity; keratin; antibacterial; controlled drug release; osteoblasts; IN-VITRO; POROUS HYDROXYAPATITE; MECHANICAL-PROPERTIES; BONE-CEMENT; FABRICATION; SCAFFOLDS; OSTEOMYELITIS; OSTEOBLASTS; INFECTION;
D O I
10.1002/jbm.b.31192
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A novel hybrid hydroxyapatite (HAP) matrix, covalently coated with rarely applied, hardly degradable keratin and effectively modified by gentanmicin immobilized in mixed-type mode (via interactions of diverse strength), was created. This hybrid showed a remarkably high drug immobilization yield and the most sustainable antibiotic release among all tested composites. It was also able to inhibit bacterial growth, both in surrounding liquid and on matrix surface, much longer (for at least 121 days of experiment) than analogous gelatin-modified and nonmodified matrices. Gentamicin-keratin-coated-HAP granules were nontoxic to human osteoblasts and enabled their proliferation with a rate similar as noncoated HAP. Presence of keratin on HAP granules seemed to slightly enhance the osteoblast proliferation. The results indicate that newly created HAP hybrid with covalently immobilized keratin and gentamicin-nontoxic and osteoblast-friendly-is a promising biomaterial of significantly prolonged antibacterial activity. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 89B: 102-113, 2009
引用
收藏
页码:102 / 113
页数:12
相关论文
共 56 条
[1]   Hydroxyapatite-coated orthopaedic screws as infection resistant materials: in vitro study [J].
Arciola, CR ;
Montanaro, L ;
Moroni, A ;
Giordano, M ;
Pizzoferrato, A ;
Donati, ME .
BIOMATERIALS, 1999, 20 (04) :323-327
[2]   Hydroxyapatite nanoceramics: Basic physical properties and biointerface modification [J].
Aronov, Daniel ;
Karlov, Anatoly ;
Rosenman, Gil .
JOURNAL OF THE EUROPEAN CERAMIC SOCIETY, 2007, 27 (13-15) :4181-4186
[3]   Plasma-sprayed carbon nanotube reinforced hydroxyapatite coatings and their interaction with human osteoblasts in vitro [J].
Balani, Kantesh ;
Anderson, Rebecca ;
Laha, Tapas ;
Andara, Melanie ;
Tercero, Jorge ;
Crumpler, Eric ;
Agarwal, Arvind .
BIOMATERIALS, 2007, 28 (04) :618-624
[4]   In vitro-in vivo characterization of gentamicin bone implants [J].
Baro, M ;
Sánchez, E ;
Delgado, A ;
Perera, A ;
Évora, C .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (03) :353-364
[5]  
Belcarz A., 2005, ENG BIOMATER, V9, P34
[6]   Effect of micro- and macroporosity of bone substitutes on their mechanical properties and cellular response [J].
Bignon, A ;
Chouteau, J ;
Chevalier, J ;
Fantozzi, G ;
Carret, JP ;
Chavassieux, P ;
Boivin, G ;
Melin, M ;
Hartmann, D .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2003, 14 (12) :1089-1097
[7]   Nanocomposites of hydroxyapatite with aspartic acid and glutamic acid and their interaction with osteoblast-like cells [J].
Boanini, Elisa ;
Torricelli, Paola ;
Gazzano, Massimo ;
Giardino, Roberto ;
Bigi, Adriana .
BIOMATERIALS, 2006, 27 (25) :4428-4433
[8]   The efficacy of a hydroxyapatite composite as a biodegradable antibiotic delivery system [J].
Buranapanitkit, B ;
Srinilta, V ;
Ingviga, N ;
Oungbho, K ;
Geater, A ;
Ovatlarnporn, C .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2004, (424) :244-252
[9]  
Cabanillas PF, 2000, INT J PHARM, V209, P15
[10]   Growth of osteoblast-like cells on porous hydroxyapatite ceramics:: an in vitro study [J].
Cerroni, L ;
Filocamo, R ;
Fabbri, M ;
Piconi, C ;
Caropreso, S ;
Condò, SG .
BIOMOLECULAR ENGINEERING, 2002, 19 (2-6) :119-124