Vancomycin release from poly(D,L-lactic acid) spray-coated hydroxyapatite fibers

被引:20
|
作者
Ravelingien, Matthieu [1 ,2 ]
Mullens, Steven [2 ]
Luyten, Jan [2 ]
D'Hondt, Matthias [3 ]
Boonen, Jente [3 ]
De Spiegeleer, Bart [3 ]
Coenye, Tom [4 ]
Vervaet, Chris
Remon, Jean Paul
机构
[1] Univ Ghent, Pharmaceut Technol Lab, Dept Pharmaceut, B-9000 Ghent, Belgium
[2] VITO NV, Mol, Belgium
[3] Univ Ghent, Drug Qual & Registrat Grp, B-9000 Ghent, Belgium
[4] Univ Ghent, Lab Pharmaceut Microbiol, B-9000 Ghent, Belgium
关键词
Hydroxyapatite; Vancomycin; Poly(D; L-lactic acid); Release profile; Biofilm formation; GROWTH-FACTORS; IMPLANTS; DEGRADATION; OSTEOMYELITIS; MATRICES; DEVICES; MICROSPHERES; DELIVERY;
D O I
10.1016/j.ejpb.2010.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The influence of the poly(D,L-lactic acid) (PDLLA) coating thickness on the in vitro vancomycin release from a hydroxyapatite (HA) carrier was studied. Microporous HA fibers with a porosity of 51 v% and an average pore diameter of 1.0 mu m were fabricated by a diffusion-induced phase separation technique. They were loaded with 38 mg vancomycin hydrochloride (VH)/g HA, and their cylindrical shape enabled the application of the spray coating technique for the deposition of uniform PDLLA coating thicknesses, varying from 6.5 mu m to 28 mu m. The resulting in vitro VH release varied from a complete release within 14 days for 6.5 mu m coatings to a release of 23% after 28 days for 28 mu m coatings. It was clear that the VH release rate from a HA fiber can be adjusted by varying the PDLLA coating thickness. Microbiological tests of these fibers against a methicillin-resistant Staphylococcus aureus (MRSA) isolate pointed to the importance of the initial burst release and confirmed that the released antibiotics had the potential to interfere with S. aureus biofilm formation. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:366 / 370
页数:5
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