Dual temperature/pH-sensitive drug delivery of poly(N-isopropylacrylamide-co-acrylic acid) nanogels conjugated with doxorubicin for potential application in tumor hyperthermia therapy

被引:129
|
作者
Xiong, Wei [1 ,2 ]
Wang, Wei [2 ]
Wang, Yi [2 ]
Zhao, Yanbing [1 ,2 ]
Chen, Huabing [1 ,2 ]
Xu, Huibi [2 ]
Yang, Xiangliang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Wuhan 430074, Peoples R China
[2] Natl Engn Res Ctr Nanomed, Wuhan 430074, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
N-isopropylacrylamide; Acrylic acid; Conjugated polymers; Doxorubicin; Drug delivery systems; Nanogels; CELLULAR UPTAKE; POLYMERIC MICELLES; ANTITUMOR-ACTIVITY; BLOCK-COPOLYMERS; IN-VIVO; NANOPARTICLES; PH; THERMO; FLUORESCENCE; RELEASE;
D O I
10.1016/j.colsurfb.2011.01.040
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper, a dual temperature/pH-sensitive poly(N-isopropylacrylamide-co-acrylic acid) nanogel (PNA) was prepared and utilized as a drug carrier. The anti-cancer drug doxorubicin (DOX) was covalent bound to PNA via an acid-labile hydrazone linkage. DOX-PNA conjugates had a pH-dependent LCST, which was 41 degrees C and 43 degrees C at pH 5.3 and 6.8 respectively, but higher than 50 degrees C at pH 7.4. The nanogels which were hydrophilic below LCST and changed to hydrophobic state above LCST possessed dual pH/temperature dependent cellular uptake and cytotoxicity. With increasing temperature, the cellular uptake of DOX-PNA was almost no difference at pH 7.4, but enhanced about 43% at pH 6.8. So the cytotoxicity of DOX-PNA also increased in higher temperature and lower pH value. It was able to distinguish tumor extracellular pH from physiological pH under hyperthermia of 43 degrees C, suggesting a great potential for anti-cancer therapy. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:447 / 453
页数:7
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