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Cytokine expression in human osteoblasts after antiseptic treatment: a comparative study between polyhexanide and
Eric Röhner1, Paula Hoff, Timo Gaber
11Department of Orthopaedics, Rudolf-Elle-Hospital, Friedrich-Schiller-University of Jena, Eisenberg, Germany.
Summary
Polyhexanide and chlorhexidine cause osteoblast cell damage. Only polyhexanide triggers inflammatory cytokine release, suggesting chlorhexidine may be preferred in septic surgery to prevent inflammation.
Area of Science:
- Biomaterials Science
- Cell Biology
- Immunology
Background:
- Chlorhexidine and polyhexanide are broad-spectrum antiseptics used in wound treatment.
- Their impact on human osteoblasts, crucial for bone health, requires further investigation.
- Understanding antiseptic effects on osteoblasts is vital for managing septic joint infections.
Purpose of the Study:
- To evaluate the in vitro effects of chlorhexidine and polyhexanide on human osteoblasts.
- To determine if these antiseptics activate inflammatory cytokine and chemokine secretion.
- To compare the osteoblast response to clinically relevant concentrations of both agents.
Main Methods:
- Human osteoblasts were isolated and cultured in vitro.
- Cells were exposed to chlorhexidine (0.1%, 2%) and polyhexanide (0.04%).
- Morphological changes were assessed via light microscopy; cytokine/chemokine secretion was quantified using multiplex arrays.
Main Results:
- Both antiseptics induced osteoblast cell damage, including shrinking and membrane defects.
- Polyhexanide, unlike chlorhexidine, significantly stimulated the secretion of multiple inflammatory mediators.
- Mediators included interleukins (1β, 6, 7), TNF-α, IFN-γ, and growth factors.
Conclusions:
- Both chlorhexidine and polyhexanide cause morphological damage to osteoblasts.
- Polyhexanide uniquely induces a significant inflammatory response in human osteoblasts.
- Chlorhexidine may be a preferred antiseptic in septic surgery to mitigate inflammatory reactions.

