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Updated: Mar 25, 2026

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Poly(trimethylene carbonate) as a carrier for rifampicin and vancomycin to target therapy-recalcitrant staphylococcal
Otto S Kluin1, Henk J Busscher1, Daniëlle Neut2
1Department of Biomedical Engineering, University of Groningen and University Medical Center Groningen, Antonius Deusinglaan 1, 9713, AV Groningen, The Netherlands.
Abstract:
Standard antibiotic therapy in osteomyelitis patients is of limited value when methicillin-resistant Staphylococcus aureus (MRSA), Staphylococcus epidermidis (MRSE), or small-colony variants (SCV) are present. Far better results are obtained by local drug delivery of antibiotic combinations including rifampicin, using a suitable carrier. We therefore investigated release kinetics of antibiotics from biodegradable poly(trimethylene carbonate) (PTMC) and in vitro biofilm inhibition of MRSA, MRSE, and S. aureus SCV strains in the course of 24, 72, and 168 h treatment by PTMC, either unloaded, gentamicin-loaded, loaded with rifampicin and fosfomycin, or rifampicin and vancomycin. PTMC appeared to be a suitable carrier for rifampicin alone or in combination with other antibiotics. Biofilm colony forming units and metabolic activity measurement (MTT assay) demonstrated significant (p < 0.05) inhibition for all strains when PTMC loaded with rifampicin and vancomycin was employed, especially after 168 h treatment. Confocal laser scanning microscopy images showed similar qualitative results. PTMC loaded with only gentamicin did not show any inhibition. This exemplifies that PTMC loaded with rifampicin and vancomycin holds promise for the treatment of recalcitrant osteomyelitis. © 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1828-1837, 2016.
Insights
Local antibiotic delivery using poly(trimethylene carbonate) (PTMC) shows promise for osteomyelitis treatment. PTMC loaded with rifampicin and vancomycin effectively inhibited biofilms from resistant bacteria, offering a better alternative to standard therapies.
Area of Science:
- Biomaterials Science
- Infectious Diseases
- Orthopedic Surgery
Background:
- Standard antibiotic therapy is often ineffective for osteomyelitis caused by resistant bacteria like methicillin-resistant Staphylococcus aureus (MRSA), methicillin-resistant Staphylococcus epidermidis (MRSE), and small-colony variants (SCV).
- Local drug delivery systems offer a potential solution for enhanced treatment efficacy in challenging osteomyelitis cases.
Purpose of the Study:
- To investigate the antibiotic release kinetics from biodegradable poly(trimethylene carbonate) (PTMC) carriers.
- To evaluate the in vitro biofilm inhibition efficacy of PTMC loaded with various antibiotic combinations against MRSA, MRSE, and S. aureus SCV strains.
Main Methods:
- Antibiotic release kinetics were studied over 24, 72, and 168 hours.
- In vitro biofilm inhibition was assessed using colony-forming unit counts and MTT metabolic activity assays.
- Confocal laser scanning microscopy was used for qualitative biofilm analysis.
Main Results:
- Poly(trimethylene carbonate) (PTMC) demonstrated suitability as a carrier for rifampicin, both alone and in combination with other antibiotics.
- PTMC loaded with rifampicin and vancomycin significantly inhibited biofilm formation (p < 0.05) for all tested strains, particularly after 168 hours.
- Gentamicin-loaded PTMC showed no significant biofilm inhibition.
Conclusions:
- Poly(trimethylene carbonate) (PTMC) loaded with rifampicin and vancomycin is a promising local drug delivery strategy for treating recalcitrant osteomyelitis.
- This approach offers superior efficacy compared to standard antibiotic therapy for infections involving resistant Staphylococcus strains.
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