The Open Orthopaedics Journal

ISSN: ― Volume ,

High Hydrostatic Pressure for Disinfection of Bone Grafts and Biomaterials: An Experimental Study

Hans Gollwitzer*, 1, Wolfram Mittelmeier2, Monika Brendle1, Patrick Weber1, 3, Thomas Miethke4, Gunther O Hofmann5, Ludger Gerdesmeyer1, Johannes Schauwecker1, Peter Diehl2
1 Klinik und Poliklinik für Orthopädie und Unfallchirurgie, Technische Universität München, Ismaninger Strasse 22, 81675 München, Germany
2 Orthopädische Klinik, Universität Rostock, Doberaner Str. 142, 18057 Rostock, Germany
3 Department of Orthopaedic Surgery, Großhadern Medical Center, Ludwig Maximilian University, Marchioninistr. 15, 81377 München, Germany
4 Institut für Medizinische Mikrobiologie, Immunologie und Hygiene, Technische Universität München, Ismaninger Strasse 22, 81675 München, Germany
5 Berufsgenossenschaftliche Kliniken "Bergmannstrost", Merseburger Str. 165, 06116 Halle (Saale), Germany



Autoclaving, heat, irradiation or chemical detergents are used to disinfect autografts, allografts and biomaterials for tissue reconstruction. These methods are often associated with deterioration of mechanical, physical, and biological properties of the bone grafts and synthetic implants. High hydrostatic pressure has been proposed as a novel method preserving biomechanical and biological properties of bone, tendon and cartilage. This is the first study to assess the inactivation of clinically relevant bacteria on biomaterials and human bone by high hydrostatic pressure.


Bacterial suspensions of Staphylococcus aureus, Pseudomonas aeruginosa and Enterococcus faecium, implants covered with infected blood, human bone infected in vitro, and biopsies of patients with chronic osteomyelitis were subjected to different protocols of high hydrostatic pressure up to 600 MPa. Bacterial survival after high hydrostatic pressure treatment was determined and compared with bacterial growth in untreated controls.


S. aureus and P. aeruginosa in suspension were completely inactivated by high hydrostatic pressure (> 5log levels), whereas E. faecium showed barotolerance up to 600 MPa. Blood and adherence to metal implants did not significantly alter inactivation of bacteria, and complete disinfection was achieved with barotolerant bacteria (S. aureus and P. aeruginosa). However, osteoarthritic bone demonstrated a non-homogeneous baroprotective effect, with single bone samples resistant to treatment resulting in unaltered bacterial growth, and complete disinfection of artificially infected bone specimens was achieved in 66% for S. aureus, 60% for P. aeruginosa and 0% for E. faecium. Human bone samples of patients with chronic osteomyelitis could be completely disinfected in 2 of 37 cases.


High hydrostatic pressure offers new perspectives for disinfection of sensitive biomaterials and bone grafts, and contamination by blood did not significantly affect bacterial inactivation rates. However, a significant baroprotective effect was demonstrated in bone. Effectiveness is currently limited to colonization and / or infection with barosensitive micro-organisms.

Keywords: High pressure, osteomyelitis, bacterial inactivation, tissue transplant, tissue graft.

Article Information

Identifiers and Pagination:

Year: 2009
Volume: 3
First Page: 1
Last Page: 7
Publisher Id: TOORTHJ-3-1
DOI: 10.2174/1874325000903010001

Article History:

Received Date: 1/12/2008
Revision Received Date: 16/12/2008
Acceptance Date: 11/1/2009
Electronic publication date: 29/1/2009
Collection year: 2009

© Gollwitzer et al.; License Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (, which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the Department for Adult Hip and Knee Reconstruction, Klinik für Orthopädie und Unfallchirurgie, Technische Universität München, Ismaninger Str., 22, D-81675 Munich, Germany; Tel: +49-89-4140-2271; Fax: +49-89-990-18319; E-mail:

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