Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (22)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Winkler, H.
Right arrow Articles by Georgopoulos, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Winkler, H.
Right arrow Articles by Georgopoulos, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (2000) 46, 423-428
© 2000 The British Society for Antimicrobial Chemotherapy

In vitro release of vancomycin and tobramycin from impregnated human and bovine bone grafts

Heinz Winklera,*, Oskar Janatab, Christian Bergera, Wolfgang Weinc and Apostolos Georgopoulosd

a Department of Orthopaedics and Central Bone Bank Vienna, b Department of Infection Control, Danube Hospital, Langobardenstrasse 122, 1220 Vienna; c Department of Clinical Pharmacology and d Clinical Department of Infections and Chemotherapy, University of Vienna, Währinger Gürtel 18–20, 1090 Vienna, Austria

In order to combine the effects of bone repair and eradication of infection, with both Grampositive and Gram-negative pathogens, the behaviour of a compound of bone graft and antibiotics was investigated. Samples of human and bovine bone, cancellous and cortical, were processed and incubated with vancomycin and tobramycin, respectively. The compound was placed in 5% human albumin and the surrounding liquid was exchanged completely every 24 h. Concentrations of antibiotics in the fluid were measured over <=28 days using high pressure liquid chromatography and a bioassay. All tested combinations eluted mainly in the initial phase with a logarithmic decrease over the testing period. The concentration of antibiotics in the albumin was well above the MIC for common pathogens throughout the investigation in all tested specimens. The highest initial concentrations were measured in the compound of bovine bone together with vancomycin (24395.8 ± 1138.9 mg/L), decreasing to 9.02 ± 1.3 mg/L after 11 exchanges. Human and bovine bone did not have significantly different properties. The storage capability of cortical bone was generally lower than that of cancellous bone. Tobramycin concentrations were significantly lower in the initial phase; however, it eluted more steadily and over a longer period, so that from day 6 onwards, its concentration was greater than that of vancomycin. After 28 days, the tobramycin concentration was 18.09 ± 2.46 mg/L (bovine cancellous bone). In conclusion, bone, if processed adequately, is an excellent carrier for vancomycin and tobramycin. Cortical bone is as suitable as cancellous bone. The pharmacokinetics of human and bovine bone are comparable. Using an antibiotic–graft compound, eradication of pathogens and grafting of bony defects may be accomplished in a one-stage procedure.

* Corresponding author. Tel: +43-664-5110556; Fax: +43-1-61679184; E-mail: heinzwinkler{at}compuserve.com


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J Bone Joint Surg BrHome page
H. Winkler, A. Stoiber, K. Kaudela, F. Winter, and F. Menschik
One stage uncemented revision of infected total hip replacement using cancellous allograft bone impregnated with antibiotics
J Bone Joint Surg Br, December 1, 2008; 90-B(12): 1580 - 1584.
[Abstract] [Full Text] [PDF]


Home page
JBJSHome page
C. Delloye, X. Banse, B. Brichard, P.-L. Docquier, and O. Cornu
Pelvic Reconstruction with a Structural Pelvic Allograft After Resection of a Malignant Bone Tumor
J. Bone Joint Surg. Am., March 1, 2007; 89(3): 579 - 587.
[Abstract] [Full Text] [PDF]


Home page
J Bone Joint Surg BrHome page
P. P. C. Khoo, K. A. Michalak, P. J. Yates, S. M. Megson, R. E. Day, and D. J. Wood
Iontophoresis of antibiotics into segmental allografts
J Bone Joint Surg Br, September 1, 2006; 88-B(9): 1149 - 1157.
[Abstract] [Full Text] [PDF]


Home page
Clin. Microbiol. Rev.Home page
H. J. Busscher and H. C. van der Mei
Microbial Adhesion in Flow Displacement Systems
Clin. Microbiol. Rev., January 1, 2006; 19(1): 127 - 141.
[Abstract] [Full Text] [PDF]


Home page
J Bone Joint Surg BrHome page
M. A. Buttaro, A. Morandi, H. G. Rivello, and F. Piccaluga
Histology of vancomycin-supplemented impacted bone allografts in revision total hip arthroplasty
J Bone Joint Surg Br, December 1, 2005; 87-B(12): 1684 - 1687.
[Abstract] [Full Text] [PDF]


Home page
J Bone Joint Surg BrHome page
R. E. Day, S. Megson, and D. Wood
Iontophoresis as a means of delivering antibiotics into allograft bone
J Bone Joint Surg Br, November 1, 2005; 87-B(11): 1568 - 1574.
[Abstract] [Full Text] [PDF]


Home page
J Bone Joint Surg BrHome page
M. A. Buttaro, R. Pusso, and F. Piccaluga
Vancomycin-supplemented impacted bone allografts in infected hip arthroplasty: TWO-STAGE REVISION RESULTS
J Bone Joint Surg Br, March 1, 2005; 87-B(3): 314 - 319.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.