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Accessing the Cytotoxicity and Cell Response to Biomaterials
Published on: July 8, 2021
Effect of polyhexanide and gentamycin on human osteoblasts and endothelial cells
Akif Ince1, Norbert Schütze, Christian Hendrich
1Department of Orthopaedic Surgery, University Hospital Würzburg, Germany. akif_ince@hotmail.com
Swiss Medical Weekly
|March 21, 2007
Summary
Antiseptic polyhexanide severely damaged bone and endothelial cells in vitro, unlike gentamicin. This suggests caution when using polyhexanide in bone cement for joint replacement infections.
Area of Science:
- Orthopedics
- Biomaterials Science
- Cell Biology
Background:
- Total joint replacement infections are challenging due to antibiotic resistance.
- Antiseptics offer broad-spectrum antimicrobial activity with limited bacterial tolerance.
- Limited research exists on antiseptic application to bone.
Purpose of the Study:
- Investigate the biocompatibility of antiseptic polyhexanide with bone-related cells.
- Evaluate the suitability of polyhexanide supplementation in bone cement for treating total arthroplasty infections.
Main Methods:
- In vitro study using human fetal osteoblast (hFOB) and endothelial (EAhy 926) cells.
- Cells exposed to varying concentrations of gentamicin and polyhexanide for six hours.
- Assessed cell viability, number, and alkaline phosphatase activity.
Main Results:
- Polyhexanide significantly reduced hFOB and endothelial cell viability and number.
- Gentamicin showed no adverse effects on cell viability or number.
- Both polyhexanide and gentamicin decreased osteogenic function (alkaline phosphatase activity) in hFOB cells.
Conclusions:
- Polyhexanide caused severe cell damage at concentrations with questionable antibacterial efficacy.
- High-dose gentamicin did not harm cells, contrasting with polyhexanide's effects.
- Findings question the use of antiseptics like polyhexanide in bone cement for arthroplasty infections; in vivo studies are needed.