posted on 2014-09-08, 00:00authored byAnja Car, Patric Baumann, Jason
T. Duskey, Mohamed Chami, Nico Bruns, Wolfgang Meier
A series of poly(dimethysiloxane)-b-poly(2-(dimethylamino)ethyl
methacrylate) (PDMS-b-PDMAEMA) block copolymers were
synthesized with atom transfer radical polymerization (ATRP). In aqueous
solution the polymers self-assembled into micelles with diameters
between 80 and 300 nm, with the ability to encapsulate DOX. The polymer
with the shortest PDMAEMA block (5 units) displayed excellent cell
viability, while micelles containing longer PDMAEMA block lengths
(13 and 22 units) led to increased cytotoxicity. The carriers released
DOX in response to a decrease in pH from 7.4 to 5.5. Confocal laser
scanning microscopy (CLSM) revealed that nanoparticles were taken
up by endocytosis into acidic cell compartments. Furthermore, DOX-loaded
nanocarriers exhibited intracellular pH-response as changes in cell
morphology and drug release were observed within 24 h.