Premium
Fabrication of Complex Micelles with Tunable Shell for Application in Controlled Drug Release
Author(s) -
Wu Chenglin,
Ma Rujiang,
He Huan,
Zhao Lizhi,
Gao Hongjun,
An Yingli,
Shi Linqi
Publication year - 2009
Publication title -
macromolecular bioscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.924
H-Index - 105
eISSN - 1616-5195
pISSN - 1616-5187
DOI - 10.1002/mabi.200900232
Subject(s) - micelle , peg ratio , copolymer , chemical engineering , chemistry , corona (planetary geology) , drug carrier , core (optical fiber) , polymer chemistry , drug delivery , materials science , polymer , organic chemistry , aqueous solution , composite material , physics , finance , astrobiology , venus , engineering , economics
At room temperature, diblock copolymers of PLA‐ b ‐PNIPAM and PEG‐ b ‐PLA self‐assembled into complex micelles with a PLA core and a mixed PEG/PNIPAM shell. By increasing the temperature, these complex micelles could be converted into a core‐shell‐corona structure composed of a PLA core, a collapsed PNIPAM shell and a soluble PEG corona, and the PEG chains stretched from the inner core to outside, leading to the formation of PEG channels. The PEG channels could be used for the exchange of substance between the core and the external environment. Compared with core‐shell micelles, complex micelles with a core‐shell‐corona structure could avoid the burst diffusion in the release of ibuprofen and inhibit the degradation of PLA by lipase to a certain extent.