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Epoxidized poly( N ‐isopropyl acrylamide)‐ b‐epo HTPB‐ b ‐poly( N ‐isopropyl acrylamide) triblock copolymer micelle nanoparticles for 10‐hydroxycamptothecin drug release
Author(s) -
Luo YanLing,
Zhang Jun,
Han FangJie,
Xu Feng,
Chen YaShao,
Liu Ru
Publication year - 2015
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.41877
Subject(s) - copolymer , materials science , polymer chemistry , micelle , dynamic light scattering , lower critical solution temperature , hydrodynamic radius , cloud point , critical micelle concentration , atom transfer radical polymerization , chemical engineering , polymerization , aqueous solution , polymer , nanoparticle , chemistry , organic chemistry , composite material , nanotechnology , engineering
Thermoresponsive poly( N ‐isopropyl acrylamide) (PNIPAM)‐ block ‐hydroxy‐terminated polybutadine‐ block ‐PNIPAM triblock copolymers were synthesized by atom transfer radical polymerization; this was followed by the in situ epoxidation reaction of peracetic acid. The copolymers were characterized by 1 H‐NMR, Fourier transform infrared spectroscopy, and size exclusion chromatography measurements, and their physicochemical properties in aqueous solution were investigated by surface tension measurement, fluorescent spectrometry, ultraviolet–visible transmittance, transmission electron microscopy observations, dynamic light scattering, and so on. The experimental results indicate that the epoxidized copolymer micelle aggregates retained a spherical core–shell micelle structure similar to the control sample. However, they possessed a decreased critical aggregate concentration (CAC), increased hydrodynamic diameters, and a high aggregation number and cloud point because of the incorporation of epoxy groups and so on. In particular, the epoxidized copolymer micelles assumed an improved loading capacity and entrapment efficiency of the drug, a preferable drug‐release profiles without an initial burst release, and a low cytotoxicity. Therefore, they were more suitable for the loading and delivery of the hydrophobic drug as a controlled release drug carrier. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41877.