Isostatic compression, a new process for incorporating vancomycin into biphasic calcium phosphate: comparison with a classical method

被引:46
作者
Gautier, H [1 ]
Merle, C [1 ]
Auget, JL [1 ]
Daculsi, G [1 ]
机构
[1] Lab Biostat, F-44035 Nantes, France
关键词
drug delivery system; vancomycin; biphasic calcium phosphate; isostatic compression; wet granulation; ceramic;
D O I
10.1016/S0142-9612(99)00139-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Isostatic compression has rarely been used to load calcium-phosphate biomaterials with therapeutic agents. This report, concerning four processes associating vancomycin, compares isostatic compression with wet granulation, a classical method. In the wet granulation study, vancomycin was associated with biphasic calcium-phosphate (BCP) granules either by adsorption or incorporation with a new granulation. In the isostatic compression study, BCP powder was compressed at 100, 140 and 200 MPa. The blocks obtained were crushed and 200-500 mu m, sieved; thus, the vancomycin solution was absorbed on these granules. Compaction of BCP and vancomycin powders gave, after crushing and sieving, granules loaded with vancomycin. In each study, 5% vancomycin was associated with BCP. Vancomycin release profiles were assessed by an in vitro culture chamber dissolution test. Physicochemical studies of BCP and vancomycin showed their structural integrity after isostatic compression. Isostatic compression prolonged vancomycin release time from 3 to 7 days and the release time became greater as isostatic pressure increased, probably because of the porosity decrease of the granules during compression. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:243 / 249
页数:7
相关论文
共 49 条
[1]  
[Anonymous], 1995, MMWR, V44, P1
[2]   CERAMIC SYSTEMS FOR LONG-TERM DELIVERY OF CHEMICALS AND BIOLOGICALS [J].
BAJPAI, PK ;
BENGHUZZI, HA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1988, 22 (12) :1245-1266
[3]  
Benoit MA, 1997, INT ORTHOP, V21, P403
[4]  
BOULER JM, IN PRESS J BIOMED MA
[5]  
Brouard S, 1997, Chirurgie, V122, P397
[6]  
DACQUET V, 1992, CLIN ORTHOP RELAT R, P241
[7]   Net-shaped hydroxyapatite implants for release of agents modulating periodontal-like tissues [J].
Denissen, H ;
vanBeek, E ;
Martinetti, R ;
Klein, C ;
vanderZee, E ;
Ravaglioli, A .
JOURNAL OF PERIODONTAL RESEARCH, 1997, 32 (01) :40-46
[8]   CERAMIC HYDROXYAPATITE IMPLANTS FOR THE RELEASE OF BISPHOSPHONATE [J].
DENISSEN, H ;
VANBEEK, E ;
LOWIK, C ;
PAPAPOULOS, S ;
VANDENHOOFF, A .
BONE AND MINERAL, 1994, 25 (02) :123-134
[9]   COMPARISON OF THE RELEASE OF GROWTH-HORMONE FROM HYDROXYAPATITE, HEAT-TREATED HYDROXYAPATITE, AND FLUOROAPATITE COATINGS ON TITANIUM [J].
DOWNES, S ;
CLIFFORD, CJ ;
SCOTCHFORD, C ;
KLEIN, CPAT .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (09) :1053-1060
[10]  
Gautier H, 1998, J BIOMED MATER RES, V40, P606, DOI 10.1002/(SICI)1097-4636(19980615)40:4<606::AID-JBM12>3.0.CO