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Temperature‐Triggered Nanosphere Formation Through Self‐Assembly of Amphiphilic Polyphosphazene
Author(s) -
Zhang Jian Xiang,
Qiu Li Yan,
Wu Xiao Li,
Jin Yi,
Zhu Kang Jie
Publication year - 2006
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.200600139
Subject(s) - polyphosphazene , amphiphile , copolymer , aqueous solution , micelle , polymer chemistry , chemistry , nanoparticle , drug delivery , chemical engineering , drug carrier , polymer , materials science , nanotechnology , organic chemistry , engineering
Summary: An amphiphilic graft polyphosphazene with a molar ratio of poly( N ‐isopropylacrylamide) (PNIPAm) to ethyl glycinate (GlyEt) of 0.54:1 was synthesized. This copolymer in aqueous solution exhibited two temperature induced phase transitions at 17.2 and 33.7 °C, which correspond to the transformation of primary aggregate morphology (at T ph1 ) and the collapse of PNIPAm chains (at T ph2 ) respectively. Network micelles were assembled in water at lower temperature (far below T ph1 ), and then narrowly dispersed nanoparticles were formed above T ph1 , while inter‐nanoparticle aggregation occurred due to the collapse of PNIPAm chains surrounding the GlyEt core when the temperature was above T ph2 . Through solubilization of the hydrophobic drug ibuprofen into polymeric aggregates at lower temperature, drug loaded nanospheres were prepared successfully. In vitro release revealed that sustained drug release was achieved with this novel delivery system. These results suggest that this novel copolymer could be used as a potential drug carrier, especially for the delivery of hydrophobic biocompounds through parenteral administration.Schematic illustration of the temperature‐triggered self‐assembly process of PNIPAm/GlyEt‐PPP in aqueous solution.