Polymerization-Induced Self-Assembly of Galactose-Functionalized Biocompatible Diblock Copolymers for Intracellular Delivery
Author(s) -
Vincent Ladmiral,
Mona Semsarilar,
Irene Cantón,
Steven P. Armes
Publication year - 2013
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja407033x
Subject(s) - chemistry , polymerization , polymersome , copolymer , drug delivery , micelle , biocompatible material , chain transfer , raft , nanotechnology , atom transfer radical polymerization , self assembly , polymer , reversible addition−fragmentation chain transfer polymerization , vesicle , radical polymerization , polymer chemistry , biophysics , aqueous solution , amphiphile , organic chemistry , materials science , membrane , biochemistry , medicine , biomedical engineering , biology
Recent advances in polymer science are enabling substantial progress in nanobiotechnology, particularly in the design of new tools for enhanced understanding of cell biology and for smart drug delivery formulations. Herein, a range of novel galactosylated diblock copolymer nano-objects is prepared directly in concentrated aqueous solution via reversible addition-fragmentation chain transfer polymerization using polymerization-induced self-assembly. The resulting nanospheres, worm-like micelles, or vesicles interact in vitro with galectins as judged by a turbidity assay. In addition, galactosylated vesicles are highly biocompatible and allow intracellular delivery of an encapsulated molecular cargo.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom