Preparation and characterization of poly(lactic-co-glycolic acid) microparticles containing DNA molecules encoding a malaria vaccine candidate
Autor: | Lina Wang, Shan Liu, Gareth M. Forde, Jenny Ho, Michael K. Danquah, Ross L. Coppel, Charles Ma |
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Rok vydání: | 2009 |
Předmět: |
Renewable Energy
Sustainability and the Environment General Chemical Engineering Organic Chemistry Nanotechnology Pollution Controlled release Inorganic Chemistry chemistry.chemical_compound PLGA Fuel Technology chemistry Zeta potential Nucleic acid Particle size Microparticle Waste Management and Disposal DNA Glycolic acid Biotechnology Nuclear chemistry |
Zdroj: | Journal of Chemical Technology & Biotechnology. 84:782-788 |
ISSN: | 1097-4660 0268-2575 |
DOI: | 10.1002/jctb.2112 |
Popis: | Background A novel ultrasonic atomization approach for the formulation of biodegradable poly(lactic-co-glycolic acid) (PLGA) microparticles of a malaria DNA vaccine is presented. A 40 kHz ultrasonic atomization device was used to create the microparticles from a feedstock containing 5 volumes of 0.5% w/v PLGA in acetone and 1 volume of condensed DNA which was fed at a flow rate of 18ml h-1. The plasmid DNA vectors encoding a malaria protein were condensed with a cationic polymer before atomization. Results High levels of gene expression in vitro were observed in COS-7 cells transfected with condensed DNA at a nitrogen to phosphate (N/P) ratio of 10. At this N/P ratio, the condensed DNA exhibited a monodispersed nanoparticle size (Z-average diameter of 60.8 nm) and a highly positive zeta potential of 38.8mV. The microparticle formulations of malaria DNA vaccine were quality assessed and it was shown that themicroparticles displayed high encapsulation efficiencies between 82-96% and a narrow size distribution in the range of 0.8-1.9 μm. In vitro release profile revealed that approximately 82% of the DNA was released within 30 days via a predominantly diffusion controlledmass transfer system. Conclusions This ultrasonic atomization technique showed excellent particle size reproducibility and displayed potential as an industrially viable approach for the formulation of controlled release particles. |
Databáze: | OpenAIRE |
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