Thermo- and pH-Induced Self-Assembly of P(AA-b-NIPAAm-b-AA) Triblock Copolymers Synthesized via RAFT Polymerization

被引:12
作者
Kuo, Chih-Yu [1 ]
Don, Trong-Ming [2 ]
Hsu, Shih-Chi [3 ]
Lee, Chia-Fen [4 ,5 ]
Chiu, Wen-Yen [1 ,3 ,6 ]
Huang, Chih-Yuan [1 ]
机构
[1] Natl Taiwan Univ, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
[2] Tamkang Univ, Dept Chem & Mat Engn, New Taipei 25137, Taiwan
[3] Natl Taiwan Univ, Dept Mat Sci & Engn, Taipei 10617, Taiwan
[4] Chia Nan Univ Pharm & Sci, Dept Cosmet Sci, Tainan 71710, Taiwan
[5] Chia Nan Univ Pharm & Sci, Inst Cosmet Sci, Tainan 71710, Taiwan
[6] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
关键词
block copolymer; core-shell particles; nanogels; reversible addition fragmentation chain transfer (RAFT); RAFT polymerization; self-assembly; stimuli-sensitive polymers; FRAGMENTATION CHAIN TRANSFER; TRIGGERED DRUG-RELEASE; BLOCK-COPOLYMERS; POLY(N-ISOPROPYLACRYLAMIDE)-BLOCK-POLY(ACRYLIC ACID); THERMORESPONSIVE PROPERTIES; RADICAL POLYMERIZATION; PHASE-TRANSITION; POLYMERS; HYDROGELS; NANOCARRIERS;
D O I
10.1002/pola.27950
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of environmentally sensitive ABA triblock copolymers with different block lengths were prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization from acrylic acid (AA) and N-isopropylacrylamide (NIPAAm). The GPC and H-1 NMR analyses demonstrated the narrow molecular weight distribution and precise chemical structure of the prepared P(AA-b-NIPAAm-b-AA) triblock copolymers owing to the controlled/living characteristics of RAFT polymerization. The lower critical solution temperature (LCST) of the triblock copolymers could be tailored by adjusting the length of PAA block and controlled by the pH value. Under heating, the triblock copolymers underwent self-assemble in dilute aqueous solution and formed nanoparticles revealed via TEM images. Physically crosslinked nanogels induced by inter-/intra-hydrogen bonding or core-shell micelle particles thus could be obtained by changing environmental conditions. With a well-defined structure and stimuli-responsive properties, the P(AA-b-NIPAAm-b-AA) copolymer is expected to be employed as a nanocarrier for biomedical applications in controlled-drug delivery and targeting therapy. (C)2015 Wiley Periodicals, Inc.
引用
收藏
页码:1109 / 1118
页数:10
相关论文
共 28 条
[1]   Temperature dependence of the colloidal stability of neutral amphiphilic polymers in water [J].
Aseyev, VO ;
Tenhu, H ;
Winnik, FM .
CONFORMATION-DEPENDENT DESIGN OF SEQUENCES IN COPOLYMERS II, 2006, 196 (1-85) :1-85
[2]   Stimuli-Induced Core-Corona Inversion of Micelle of Poly(acrylic acid)-block-Poly(N-isopropylacrylamide) and Its Application in Drug Delivery [J].
Bastakoti, Bishnu Prasad ;
Guragain, Sudhina ;
Nakashima, Kenichi ;
Yamauchi, Yusuke .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2015, 216 (03) :287-291
[3]   INTERACTION BETWEEN CALCIUM, A MODEL DIVALENT-CATION, AND A RANGE OF POLY(ACRYLIC ACID) RESINS AS A FUNCTION OF SOLUTION PH [J].
CHARMAN, WN ;
CHRISTY, DP ;
GEUNIN, EP ;
MONKHOUSE, DC .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1991, 17 (02) :271-280
[4]   Dual Stimuli-Responsive Polymeric Hollow Nanogels Designed as Carriers for Intracellular Triggered Drug Release [J].
Chiang, Wen-Hsuan ;
Viet Thang Ho ;
Huang, Wen-Chia ;
Huang, Yi-Fong ;
Chern, Chorng-Shyan ;
Chiu, Hsin-Cheng .
LANGMUIR, 2012, 28 (42) :15056-15064
[5]   Living free-radical polymerization by reversible addition-fragmentation chain transfer: The RAFT process [J].
Chiefari, J ;
Chong, YK ;
Ercole, F ;
Krstina, J ;
Jeffery, J ;
Le, TPT ;
Mayadunne, RTA ;
Meijs, GF ;
Moad, CL ;
Moad, G ;
Rizzardo, E ;
Thang, SH .
MACROMOLECULES, 1998, 31 (16) :5559-5562
[6]   Poly(N-isopropylacrylamide)-block-poly(acrylic acid) hydrogels: synthesis and rapid thermoresponsive properties [J].
Cong, Houluo ;
Zheng, Sixun .
COLLOID AND POLYMER SCIENCE, 2014, 292 (10) :2633-2645
[7]   Polymerization-induced thermal self-assembly (PITSA) [J].
Figg, C. Adrian ;
Simula, Alexandre ;
Gebre, Kalkidan A. ;
Tucker, Bryan S. ;
Haddleton, David M. ;
Sumerlin, Brent S. .
CHEMICAL SCIENCE, 2015, 6 (02) :1230-1236
[8]   New polymer synthesis by nitroxide mediated living radical polymerizations [J].
Hawker, CJ ;
Bosman, AW ;
Harth, E .
CHEMICAL REVIEWS, 2001, 101 (12) :3661-3688
[9]   Exploring the Volume Phase Transition Behavior of POEGA- and PNIPAM-Based Core-Shell Nanogels from Infrared-Spectral Insights [J].
Hou, Lei ;
Ma, Kai ;
An, Zesheng ;
Wu, Peiyi .
MACROMOLECULES, 2014, 47 (03) :1144-1154
[10]   Aqueous Reversible Addition-Fragmentation Chain Transfer Dispersion Polymerization of Thermoresponsive Diblock Copolymer Assemblies: Temperature Directed Morphology Transformations [J].
Kessel, Stefanie ;
Truong, Nghia P. ;
Jia, Zhongfan ;
Monteiro, Michael J. .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2012, 50 (23) :4879-4887