Abstract
This contribution describes a simple, aerosol-based method for fabricating monodisperse particles containing mixtures of poly(lactide-co-glycolic acid) [PLGA], protamine sulfate (Prot), and poly(l-lysine) [PLL] as nanocarriers for gene transfection. Aqueous solutions of PLGA, Prot, and PLL were collison-atomized, and the resulting aerosolized droplets were dried "on the fly" to form solid particles, which then were electrostatically size-classified into 50, 100, and 200 nm mobility diameter samples. Measurements of cell viability and transfection reveal that the fabricated nanocarriers have a lower cytotoxicity (>85% in cell viability) and a higher transfection efficiency [>8.7 × 105 in relative light units (RLU) mg -1] than does 25 kDa polyethyleneimine (≈50% and 6.8 × 105 RLU mg-1). One-step fabrication of monodisperse PLGA-based mixture polymer nanocarriers is demonstrated using a single-pass aerosol system, a collison atomizer, and a nano differential mobility analyzer. This allows the generation of monodisperse polymeric nanocarriers in a simple manner. This strategy can be applied as a new platform for polymeric nanocarrier preparation without wet and time- consuming chemical routes.
| Original language | English |
|---|---|
| Pages (from-to) | 1840-1844 |
| Number of pages | 5 |
| Journal | Macromolecular Rapid Communications |
| Volume | 33 |
| Issue number | 21 |
| DOIs | |
| State | Published - 2012.11.14 |
Keywords
- gene transfection
- monodisperse
- nanoparticles
- particle size distribution
- poly(lactide-co-glycolic acid)-based nanocarriers
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