摘要
Biocompatible and biodegradable thermoresponsive polymers are of great interest in “smart” biomedical applications. Herein, triblock copolymers (6a and 6b) comprised of hydrophobic poly(propylene glycol) (PPG) and OEGylated polypeptides bearing Y-shaped or linear pendants are prepared by ring-opening polymerization of reactive N -carboxyanhydride monomers and subsequent side chain modification of polypeptides. OEGylated triblock copolymer bearing Y-shaped (6a) or linear pendants (6b) with similar main chain length and the same amount of oligo(ethylene glycol) (OEG) units are successfully prepared as verified by 1 H NMR, FTIR, and GPC. CD analysis reveals that 6a with Y-shaped OEG pendants shows thermal- or salt-induced destabilization of α-helical conformation in water. Both 6a and 6b show reversible lower critical solution temperature (LCST)-type phase transitions in DI H 2 O or PBS. Incorporation of a PPG segment leads to a significant decrease of the LCST-type cloud point temperature ( T cp ). Consequently, 6a and 6b show T cp to human body temperature at low polymer concentrations (≤0.5 mg mL −1 in PBS). Moreover, 6a and 6b show low in vitro cytotoxicity and biodegradability in the presence of proteinase K. The results indicate that the thermoresponsive properties of LCST-type polymers can be readily tuned by constructing Y-shaped pendants as well as incorporation of hydrophobic polymer building blocks.
危险品化学品经营许可证(带存储)