In vivo efficiency of antimicrobial inorganic bone grafts in osteomyelitis treatments
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
30678975
DOI
10.1016/j.msec.2018.11.064
PII: S0928-4931(18)30864-6
Knihovny.cz E-resources
- Keywords
- Calcium phosphate cements, Calcium phosphate foams, Drug delivery, In vivo, Magnesium phosphate cements, Osteomyelitis,
- MeSH
- Anti-Bacterial Agents administration & dosage pharmacokinetics pharmacology MeSH
- Doxycycline administration & dosage pharmacology MeSH
- Femur diagnostic imaging pathology MeSH
- Calcium Phosphates chemistry MeSH
- Drug Implants chemistry pharmacology MeSH
- Bone Diseases, Infectious drug therapy therapy MeSH
- Bone Cements chemistry pharmacology MeSH
- Rabbits MeSH
- Drug Delivery Systems methods MeSH
- Osteomyelitis drug therapy therapy MeSH
- Porosity MeSH
- Bone Regeneration drug effects MeSH
- Staphylococcal Infections drug therapy therapy MeSH
- Drug Liberation MeSH
- Viscoelastic Substances chemistry MeSH
- Treatment Outcome MeSH
- Animals MeSH
- Check Tag
- Rabbits MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- calcium phosphate MeSH Browser
- Doxycycline MeSH
- Calcium Phosphates MeSH
- Drug Implants MeSH
- Bone Cements MeSH
- Viscoelastic Substances MeSH
The purpose of the present work was to evaluate in vivo different antimicrobial therapies to eradicate osteomyelitis created in the femoral head of New Zealand rabbits. Five phosphate-based cements were evaluated: calcium phosphate cements (CPC) and calcium phosphate foams (CPF), both in their pristine form and loaded with doxycycline hyclate, and an intrinsic antimicrobial magnesium phosphate cement (MPC; not loaded with an antibiotic). The cements were implanted in a bone previously infected with Staphylococcus aureus to discern the effects of the type of antibiotic administration (systemic vs. local), porosity (microporosity, i.e. <5 μm vs. macroporosity, i.e. >5 μm) and type of antimicrobial mechanism (release of antibiotic vs. intrinsic antimicrobial activity) on the improvement of the health state of the infected animals. A new method was developed, with a more comprehensive composite score that integrates 5 parameters of bone infection, 4 parameters of bone structural integrity and 4 parameters of bone regeneration. This method was used to evaluate the health state of the infected animals, both before and after osteomyelitis treatment. The results showed that the composite score allows to discern statistically significant differences between treatments that individual evaluations were not able to identify. Despite none of the therapies completely eradicated the infection, it was observed that macroporous materials (CPF and CPFd, the latter loaded with doxycycline hyclate) and intrinsic antimicrobial MPC allowed a better containment of the osteomyelitis. This study provides novel insights to understand the effect of different antimicrobial therapies in vivo, and a promising comprehensive methodology to evaluate the health state of the animals was developed. We expect that the implementation of such methodology could improve the criteria to select a proper antimicrobial therapy.
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