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Hydroxy-urea bearing albumin microspheres--preparation, characterization and evaluation
S K Pande1, S P Vyas, V K Dixit
1Department of Pharmaceutical Sciences, Dr H. S. Gour Vishwavidyalaya, Sagar (M.P.), India.
Journal of Microencapsulation
|January 1, 1991
Summary
Magnetic albumin microspheres successfully deliver hydroxyurea, showing enhanced stability and targeted delivery. These novel microspheres demonstrate significant potential for improved drug localization and therapeutic outcomes.
Area of Science:
- Biomedical Engineering
- Materials Science
- Pharmacology
Background:
- Hydroxyurea is a crucial drug with limitations in stability and targeted delivery.
- Albumin microspheres offer a promising platform for drug delivery applications.
- Magnetic nanoparticles can enhance drug localization and retention at target sites.
Purpose of the Study:
- To develop and characterize hydroxyurea-loaded albumin microspheres using glycerol as an internal phase.
- To incorporate silicone-coated magnetite nanoparticles for magnetic targeting.
- To evaluate the in vitro drug release, in vivo distribution, and stability of the magnetic albumin microspheres.
Main Methods:
- Polymer dispersion method utilizing glycerol in a water-in-oil emulsion.
- Incorporation of silicone-coated magnetite nanoparticles into human serum albumin (HSA) microspheres.
- In vitro drug release studies and in vivo biodistribution analysis in a rat model with an applied magnetic field.
Main Results:
- Microspheres exhibited controlled in vitro hydroxyurea release, linearly correlated with the square root of time.
- Significant localization (67%) of magnetic albumin microspheres achieved in a rat tail segment using an 8000 Oe magnetic field.
- Enhanced stabilization of hydroxyurea within the microspheres compared to conventional methods.
Conclusions:
- Glycerol-based albumin microspheres are effective for hydroxyurea delivery.
- Magnetic targeting significantly improves drug localization in vivo.
- The developed magnetic albumin microspheres demonstrate superior drug stabilization and targeted delivery potential.