Abstract
Abstract summary Poly(lactide-co-glycolide) (PLGA) nanoparticles were prepared via a modified emulsion solvent diffusion (ESD) method and a double emulsion method as potential nanocarriers for the systemic and lymphatic oral delivery of insulin and ovalbumin respectively. The effect of key process parameters on the size distribution of the PLGA nanoparticles was assessed.
Full Text
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call