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Published on: December 27, 2013
MBG/PLGA composite microspheres with prolonged drug release
Xia Li1, Xiupeng Wang, Lingxia Zhang
1State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, People's Republic of China.
Abstract:
Mesoporous bioactive glass (MBG) and composite microspheres with MBG particles embedded in biodegradable poly(D,L-lactide-co-glycolide) (PLGA) matrix have been prepared and used to load gentamicin (GS). The in vitro drug release experiments from both MBG and composite microspheres were conducted in distilled water and phosphate buffered saline (PBS) solution at 37 degrees C for more than 30 days. In both water and PBS, GS release from the MBG was very fast with about 60 wt % of the loaded drug released in the first 24 h, and more than 80 wt % released in two days. MBG/PLGA composite microspheres showed an initial release of about 33 wt % in the first day, and 48 wt % in 2 days, and a subsequent sustained release lasting for more than 4 weeks in PBS. MBG/PLGA composite microspheres may be used as an alternative drug release system, especially as a bone void filler for bone repair due to their combined advantages of sustained release of antibiotics and apatite-forming ability.
Insights
Mesoporous bioactive glass/poly(D,L-lactide-co-glycolide) composite microspheres offer sustained gentamicin release for over 4 weeks. This makes them promising for bone repair applications, combining antibiotic delivery with bone regeneration properties.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Regenerative Medicine
Background:
- Mesoporous bioactive glasses (MBG) are investigated for drug delivery.
- Biodegradable polymers like poly(D,L-lactide-co-glycolide) (PLGA) are used in biomedical applications.
- Gentamicin (GS) is a common antibiotic for bone infections.
Purpose of the Study:
- To prepare and characterize MBG and MBG/PLGA composite microspheres for gentamicin loading.
- To evaluate the in vitro drug release kinetics of gentamicin from these microspheres.
- To assess the potential of MBG/PLGA composites as drug delivery systems for bone repair.
Main Methods:
- Preparation of MBG and MBG/PLGA composite microspheres.
- Loading of gentamicin (GS) into the microspheres.
- In vitro drug release studies in distilled water and phosphate-buffered saline (PBS) at 37°C for over 30 days.
Main Results:
- MBG microspheres exhibited rapid GS release: ~60% in 24h and >80% in 2 days.
- MBG/PLGA composite microspheres showed an initial release of ~33% in 1 day and ~48% in 2 days.
- Composite microspheres demonstrated sustained GS release for over 4 weeks in PBS.
Conclusions:
- MBG/PLGA composite microspheres provide sustained antibiotic release, unlike pure MBG.
- These composites are potential candidates for bone void fillers, offering combined antibiotic delivery and osteoconductive properties.
- The sustained release profile is advantageous for preventing bone infections and promoting bone healing.
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