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Updated: Apr 21, 2026

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
Diblock copolymers of polyethylene glycol and a polymethacrylamide with side-chains containing twin ortho ester
Xiaojing Zhou1, Shi Luo, Rupei Tang
1School of Pharmaceutical Science, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu Province, 214122, P. R. China.
Abstract:
The diblock copolymer, PEG-b-PMEA, was synthesized by reversible-addition fragmentation chain transfer polymerization (RAFT). The PMEA block contained a polymethacrylamide backbone and twin ortho ester rings in the side-chains. At neutral pH, PEG-b-PMEA self-assembled to form stable micelles. At pH 5, the twin ortho ester rings were quickly hydrolyzed to completion in 12 h, and releasing nearly 70% of the encapsulated Nile Red dye. The PEG-b-PMEA micelles were completely nontoxic to cultured cells as determined by the MTT assay. Paclitaxel (PTX)-loaded micelles showed toxicity toward lung cancer cells comparable to that of the free PTX at equivalent doses. These results suggest that the PEG-b-PMEA micelles could be useful nano-carriers for pH-responsive delivery of poorly soluble anticancer drugs.
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