Galactosamine-modified PEG-PLA/TPGS micelles for the oral delivery of curcumin

In this study, galactosamine-modified poly(ethylene glycol)-poly(lactide) (Gal-PEG-PLA) polymers were synthesized and Gal-PEG-PLA/D-alpha-tocopherol polyethylene glycol 1000 succinate (TPGS) micelles named as GPP micelles were designed to promote the oral absorption of a hydrophobic drug, curcumin (CUR). CUR-loaded GalPEG-PLA/TPGS micelles (CUR@GPP micelles) were fabricated using the thin-film dispersion method. CUR@GPP micelles had a size of about 100 nm, a near-neutral zeta potential, drug loading (DL) of 14.6%, and sustained release properties. GPP micelles with high Gal density (GPP3 micelles) were superior in facilitating uptake in epithelial cells and improving intestinal permeation. In situ intestinal absorption studies suggested that the jejunum and ileum were the best absorption segments in the intestinal tract. Additionally, biodistribution results revealed that GPP3 micelles could be remarkably taken up by the jejunum and ileum. Pharmacokinetics revealed that the maximum plasma concentration (C-max) and the area under the plasma concentration-time curve from 0 to 24 h (AUC(0-24)) for CUR@GPP3 micelles were both significantly increased, and that the relative bioavailability of CUR@GPP3 micelles to CUR-loaded mPEG-PLA/TPGS micelles (CUR@PP micelles) was 258.8%. Furthermore, CUR-loaded micelles could reduce damage to the liver and intestinal tissues. This study highlights the importance of Gal content in the design of targeting nanocarrier Gal-modified micelles, which have broad prospects for oral delivery of hydrophobic drugs. Therefore, they could serve as a promising candidate for targeted delivery to the liver.

Automated summary

Galactosamine-modified poly(ethylene glycol)-poly(lactide) polymers were synthesized in this study to design Gal-PEG-PLA/D-alpha-tocopherol polyethylene glycol 1000 succinate (TPGS) micelles for improving the oral absorption of curcumin. The high Gal density GPP3 micelles showed superior uptake in epithelial cells, improved intestinal permeation, and reduced damage to liver and intestinal tissues. These Gal-modified micelles have promising prospects for oral delivery of hydrophobic drugs and targeted delivery to the liver.