| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 601116 | Colloids and Surfaces B: Biointerfaces | 2011 | 5 Pages |
Nanoparticles effectively deliver therapeutic agent by penetrating into the skin. Indomethacin (IM) and coumarin-6 were loaded in PLGA nanoparticles with an average diameter of 100 nm. IM and coumarin-6 were chosen as a model drug and as a fluorescent marker, respectively. The surfaces of the nanoparticles were negatively charged. Permeability of IM-loaded PLGA nanoparticles through rat skin was studied. Higher amount of IM was delivered through skin when IM was loaded in nanoparticles than IM was free molecules. Also, iontophoresis was applied to enhance the permeability of nanoparticles. When iontophoresis with 3 V/cm was applied, permeability of IM was much higher than that obtained by simple diffusion of nanoparticles through skin. The combination of charged nanoparticle system with iontophoresis is useful for effective transdermal delivery of therapeutic agents.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Indomethacin/PLGA nanoparticles effectively delivered indomethacin through rat skin. ► Iontophoresis enhanced permeability of indomethacin/PLGA nanoparticles through rat skin. ► PLGA nanoparticles permeated through stratum corneum and reached to stratum germinativum.
