Category
Bioactive Materials: Theranostics and Cancer Nanotechnologies
Year
2012
Institutions
Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA 02115
Summary
To increase the solubility, bioavailablity and targetability of the water insoluble drug, paclitaxel (PTX), we synthesized a novel amphiphilic PEG-PTX conjugate with the matrix metalloprotease 2-sensitive peptide link between PEG and PTX, which was incorporated into novel nanocarrier system. Our system is a self-assembled micellar nanocarrier (Fig.1) containing three amphiphilic PEGbased conjugates, PEG(2000)-peptide- PTX, PEG(1000)-PE, and TATp-PEG(1000)- DOPE. Compared to conventional micellar drug delivery systems, this design ensures: i) a high drug loading efficiency, ii) an increased micelle stability, iii) an increased drug targetability, and iv) an enhanced drug internalization by the tumor cells.