F. Hoffmann et al., PREPARATION, CHARACTERIZATION AND CYTOTOXICITY OF METHYLMETHACRYLATE COPOLYMER NANOPARTICLES WITH A PERMANENT POSITIVE SURFACE-CHARGE, International journal of pharmaceutics, 157(2), 1997, pp. 189-198
Methylmethacrylate copolymer nanoparticles containing different cation
ic comonomers such as N-trimethylammoniumethylmethacrylate (TMAEMC), N
-dimethylammoniumethylmethacrylate (DMAEMC), N-trimethylammoniumpropyl
methylacrylamide (MAPTAC) or the anionic comonomer sulfopropylmethacry
late (SPM), respectively, were prepared by free radical polymerization
. Particle size was determined by photon correlation spectroscopy (PCS
), transmission and scanning electron microscopy (TEM, SEM), and surfa
ce charge by microelectrophoresis. Pure poly(methylmethacrylate) nanop
articles served as control. Depending on the method, mean diameters of
permanently positively-charged nanoparticles MMA-TMAEMC and MMA-MAPTA
C were 243 or 207 nm (PCS), 161 or 201 nm (TEM), and 158 or 197 nm (SE
M), respectively. Zeta potential examined in demineralized water or Na
Cl solution was +63.4 or +32.1 mV for MMA-TMAEMC nanoparticles and +49
.2 or +32.0 mV for MMA-MAPTAC nanoparticles, respectively. Cytotoxicit
y of nanoparticles was determined by MTT assay in three different cell
cultures including human foreskin fibroblasts (HFF) and two monkey ki
dney cell lines MA-104 and Vero. Cell viability profiles of TMAEMC and
MAPTAC containing nanoparticles were different, showing IC50 values f
or MMA-TMAEMC nanoparticles of 189.6 +/- 11.4 mu g/ml (MA-104), 110.9
+/- 3.1 mu g/ml (Vero) and 27.2 +/- 4.0 mu g/ml (HFF). Cell viability
at maximum concentration of 500 mu g/ml MMA-MAPTAC nanoparticles was 9
8.3% (Vero), 85.7% (MA-104), or 94.0% (HFF), respectively. (C) 1997 El
sevier Science B.V.