Characterization of chlorhexidine-releasing, fast-setting, brushite bone cements

被引:47
作者
Young, Anne M. [1 ]
Ng, Poon Yun J. [1 ]
Gbureck, Uwe [2 ]
Nazhat, Showan N. [3 ]
Barralet, Jake E. [4 ]
Hofmann, Michael P. [5 ]
机构
[1] UCL Eastman Dent Inst, Div Biomat & Tissue Engn, London WC1X 8LD, England
[2] Univ Wurzburg, Dept Funct Mat Med & Dent, D-97070 Wurzburg, Germany
[3] McGill Univ, Dept Min & Mat Engn, Montreal, PQ H3A 2B2, Canada
[4] McGill Univ, Fac Dent, Montreal, PQ H3A 2B2, Canada
[5] Univ Birmingham, Sch Dent, Biomat Unit, Birmingham B4 6NN, W Midlands, England
关键词
brushite; chlorhexidine; drug release; drug cement interaction; setting kinetics;
D O I
10.1016/j.actbio.2007.12.009
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The effect of antibacterial chlorhexidine diacetate powder (CHX) on the setting kinetics of a brushite-forming P-tricalcium phosphate/monocalcium. phosphate monohydrate (beta-TCP/MCPM) cement was monitored using attenuated total reflection Fourier transform infrared spectroscopy. The final composition of the set cement with up to 12 wt.% CHX content before and after submersion in water for 24 h, the kinetics of chlorhexidine release and the total sample mass change in water over four weeks was monitored using Raman mapping, UV spectroscopy and gravimetry, respectively. Below 9 wt.%, CHX content had no significant effect on brushite formation rate at 37 degrees C, but at 12 wt.% the half-life of the reaction decreased by one-third. Raman mapping confirmed that brushite was the main inorganic component of the set cements irrespective of CHX content, both before and after submersion in water. The CHX could be detected largely as discrete solid particles but could also be observed partially dispersed throughout the pores of the set cement. The percentage of CHX release was found to follow Fick's law of diffusion, being independent of its initial concentration, proportional to the square root of time and, with I mm thick specimens, 60% was released at 24 h. Total set cement mass loss rate was not significantly affected by CHX content. On average, cements exhibited a loss of 7 wt.% assigned largely to surface phosphate particle loss within the initial 8 h followed by 0.36 wt.% per day. (C) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1081 / 1088
页数:8
相关论文
共 32 条
[1]   Controlled release of chlorhexidine from UDMA-TEGDMA resin [J].
Anusavice, K. J. ;
Zhang, N. -Z. ;
Shen, C. .
JOURNAL OF DENTAL RESEARCH, 2006, 85 (10) :950-954
[2]   Ionic modification of calcium phosphate cement viscosity. Part II: hypodermic injection and strength improvement of brushite cement [J].
Barralet, JE ;
Grover, LM ;
Gbureck, U .
BIOMATERIALS, 2004, 25 (11) :2197-2203
[3]   Technological issues for the development of more efficient calcium phosphate bone cements: A critical assessment [J].
Bohner, M ;
Gbureck, U ;
Barralet, JE .
BIOMATERIALS, 2005, 26 (33) :6423-6429
[4]   Gentamicin-loaded hydraulic calcium phosphate bone cement as antibiotic delivery system [J].
Bohner, M ;
Lemaitre, J ;
VanLanduyt, P ;
Zambelli, PY ;
Merkle, HP ;
Gander, B .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (05) :565-572
[5]   In vitro aging of a calcium phosphate cement [J].
Bohner, M ;
Merkle, HP ;
Lemaître, J .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2000, 11 (03) :155-162
[6]   Effects of sulfate, pyrophosphate, and citrate ions on the physicochemical properties of cements made of beta-tricalcium phosphate-phosphoric acid-water mixtures [J].
Bohner, M ;
Lemaitre, J ;
Ring, TA .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1996, 79 (06) :1427-1434
[7]  
Bohner M, 2000, INJURY, V31, pS37
[8]  
Bohner M, 2000, J PHARM SCI, V89, P1262, DOI 10.1002/1520-6017(200010)89:10<1262::AID-JPS4>3.3.CO
[9]  
2-Z
[10]  
Crank J., 1957, The Mathematics of Diffusion