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A β-Cyclodextrin-Eugenol Complex as a Modifier of Methacrylate Bone Cement.
Grzegorz Przesławski1, Katarzyna Szcześniak1, Antonino Mazzaglia2
1Poznan University of Technology, Faculty of Chemical Technology, Poznan, Poland.
Summary
This study developed a β-cyclodextrin/eugenol complex (CP-EU) to improve methacrylic bone cement. The CP-EU complex enhances mechanical strength and provides antibacterial properties without compromising safety, offering a potential antibiotic alternative.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Orthopedic Surgery
Background:
- Antibiotics in bone cement can lead to resistance; eugenol offers antimicrobial potential.
- Eugenol's polymerization retardation necessitates modification for effective use in bone cement.
- Sulfobutylether-β-cyclodextrin (Captisol) was explored as a complexing agent for eugenol.
Purpose of the Study:
- To investigate the impact of a β-cyclodextrin/eugenol complex (CP-EU) on methacrylic bone cement properties.
- To assess the mechanical strength, polymerization characteristics, and antibacterial efficacy of modified bone cement.
- To evaluate the biocompatibility and osteoblast viability in the presence of the CP-EU complex.
Main Methods:
- Formulation of methacrylic bone cement incorporating the CP-EU complex.
- Evaluation of polymerization parameters (doughing time, Tmax, Tset, tset).
- Assessment of mechanical properties (compressive strength, Young's modulus), eugenol release kinetics, antibacterial activity against E. coli, and cytotoxicity on osteoblasts.
Main Results:
- The CP-EU complex (0.5 wt%) eliminated eugenol's negative effect on polymerization, maintaining clinically acceptable temperatures (58.7°C-69.8°C) and meeting ISO 5833:2002 standards.
- Significant enhancement in mechanical properties observed: compressive strength increased by up to 33.5%, and Young's modulus by up to 454.1%.
- High eugenol release (84.5%-86.9%) and potent antibacterial activity against E. coli demonstrated. Complexation with Captisol restored biocompatibility, improving osteoblast viability compared to free eugenol.
Conclusions:
- The CP-EU complex effectively modifies bone cement, enhancing mechanical performance and providing desirable antimicrobial properties.
- Captisol complexation successfully modulates eugenol release and improves biocompatibility, addressing cytotoxicity concerns of free eugenol.
- Modified bone cements meet standard requirements, exhibiting good mechanical properties, high eugenol release, and antibacterial efficacy, positioning CP-EU as a promising alternative to antibiotic-loaded cements.
Keywords:
antibacterial agentsantibacterial propertiesbone cementscaptisoldrug releaseeugenolβ‐cyclodextrin
