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Updated: Jun 20, 2026

Methionine Functionalized Biocompatible Block Copolymers for Targeted Plasmid DNA Delivery
Published on: August 6, 2019
Poly(ethylene glycol)-block-poly(glycidyl methacrylate) with oligoamine side chains as efficient gene vectors
Ming Ma1, Feng Li, Fu-jie Chen
1Key Laboratory of Biomedical Polymers of Ministry of Education, College of Chemistry and Molecular Science, Wuhan University, Wuhan 430072, P. R. China.
Abstract:
Well-defined diblock copolymers, poly(ethylene glycol)-block-poly(glycidyl methacrylate)s (PEG-b-PGMAs), with different poly(glycidyl methacrylate) (PGMA) chains, were prepared via atom transfer radical polymerization (ATRP) from the same macromolecular initiator 2-bromoisobutyryl-terminated poly(ethylene glycol) (PEG). Ethyldiamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), and polyethyleneimine (PEI) with an M(W) of 400 (PEI(400)) were used to decorate PEG-b-PGMAs to get the cationic polymers PEG-b-PGMA- oligoamines. These cationic polymers possessed high buffer capability and could condense plasmid DNA (pDNA) into nanoscaled complexes of 125-530 nm. These complexes showed the positive zeta potential of 20-35 mV at N/P ratios of 10-50. Most of them exhibited very low cytotoxicity and good transfection efficiency in 293T cells. The presence of the serum medium did not decrease the transfection efficiency due to the steric stabilization of the PEG chains.
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