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Silk coating on poly(ε-caprolactone) microspheres for the delayed release of vancomycin
Jian Zhou1, TaoLin Fang, Jianchuan Wen
1Department of Orthopaedic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Abstract:
The treatment of osteomyelitis remains a challenge for orthopaedic surgeons. Controlled release of vancomycin from biodegradable microspheres is a promising method for eliminating infection. However, the large initial burst release may make it difficult to maintain the local vancomycin concentration superior to minimum inhibitory concentration for several weeks. The aims of this study were to explore applications of the silk fibroin (SF) as an aqueous coating material for vancomycin-loaded poly(ε-caprolactone) (PCL) microspheres, and investigate the effects of silk coating on in vitro drug release. Examinations of particle size analyses, vancomycin content, Fourier transform infrared spectroscopy, differential scanning calorimetry, scanning electron microscopy and in vitro drug release were performed. The results showed that silk coating could reduce the large initial burst release and retard the vancomycin release. Therefore, we suggest that the SF could be used as an aqueous coating material for vancomycin-loaded PCL microspheres and prolonged the drug release. SF coating on vancomycin-loaded PCL microspheres may be considered as an effective approach to prolong the drug release and improve the anti-infection effects.
Insights
Silk fibroin coating effectively reduces initial vancomycin burst release from poly(ε-caprolactone) microspheres. This silk coating prolongs drug delivery, potentially improving osteomyelitis treatment outcomes.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Orthopaedic Surgery
Background:
- Osteomyelitis treatment is challenging, with controlled vancomycin release from microspheres showing promise.
- Large initial burst release from vancomycin-loaded poly(ε-caprolactone) (PCL) microspheres can hinder sustained therapeutic levels.
- Maintaining drug concentration above the minimum inhibitory concentration for extended periods is crucial for effective infection elimination.
Purpose of the Study:
- To explore silk fibroin (SF) as an aqueous coating for vancomycin-loaded PCL microspheres.
- To investigate the impact of SF coating on in vitro vancomycin release kinetics.
- To assess the potential of SF coating for improving drug delivery in osteomyelitis treatment.
Main Methods:
- Preparation and characterization of vancomycin-loaded PCL microspheres with and without SF coating.
- Analysis of particle size, vancomycin content, and material properties using FTIR and DSC.
- Scanning electron microscopy (SEM) for surface morphology evaluation.
- In vitro drug release studies to assess release profiles over time.
Main Results:
- Silk fibroin coating successfully reduced the initial burst release of vancomycin.
- SF coating significantly retarded the overall vancomycin release rate from PCL microspheres.
- Characterization confirmed the integrity and composition of the coated microspheres.
Conclusions:
- Silk fibroin serves as an effective aqueous coating material for vancomycin-loaded PCL microspheres.
- SF coating offers a viable strategy to prolong vancomycin release, addressing limitations of burst release.
- This approach holds potential for enhancing anti-infection effects in osteomyelitis management through sustained drug delivery.
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