Self-assembled micellar nanoparticles of a novel star copolymer for thermo and pH dual-responsive drug release

被引:82
作者
Liu, Yunhai [1 ]
Cao, Xiaohong [1 ]
Luo, Mingbiao [1 ]
Le, Zhanggao [1 ]
Xu, Wenyuan [1 ]
机构
[1] E China Inst Technol, Dept Appl Chem, Fuzhou 344000, Peoples R China
基金
中国国家自然科学基金;
关键词
N-isopropylacrylamide; N; N-dimethylaminoethylmethacrylate; Micellar nanoparticles; Dual-responsive; Drug delivery; POLYMERIC MICELLES; BLOCK-COPOLYMERS; DELIVERY-SYSTEMS; GENE DELIVERY; TUMOR PH; NANOCARRIERS; MICELLIZATION; CHEMOTHERAPY; RELEVANT; DESIGN;
D O I
10.1016/j.jcis.2008.10.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An amphiphilic star block copolymer comprised of a hydrophobic PMMA block and a hydrophilic triarm poly(NIPAAm-co-DMAEMA) block was synthesized by copolymerization of NIPAAm and DMAEMA, with Ce(4+) ions and tris(hydroxymethyl)methylamine as a redox initiatory system. The star copolymer undergoes self-assembly to the micellar nanoparticles with a core-shell structure and the thermo/pH dual-response, originated from the thermo-sensitivity of PNIPAAm and the pH-sensitivity of PDMAEMA. A fluorescence probe study showed the pH-dependent low CMCs (7.5 to 11.2 mg/L) of the micelles, confirming the formation of stable micelles. Morphological investigations showed that the blank and drug-loaded micelles both had spherical and uniform shapes. The sizes of the blank and drug-loaded nanoparticles were between 80 and 120 nm, depending on the given pH. The LCSTs of the star copolymer were determined to be 32 degrees C, 36.6 degrees C and 39.5 degrees C, corresponding to pH 5, pH 7.4 and pH 9, respectively, demonstrating a pH-dependent thermo-response. As a drug delivery, the micellar nanoparticles showed the dual-responsive release profiles in vitro, which were confirmed by the drug release studies. The obtained results showed the thermo-triggered accelerated release at pH 7.4, and the pH-triggered accelerated release at 37 degrees C, indicating the micelles nanoparticles would be a promising site-specific drug delivery for enhancing the accumulation of drug in targeting pathological areas. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:244 / 252
页数:9
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