Multifunctioning pH-Responsive Nanoparticles from Hierarchical Self-Assembly of Polymer Brush for Cancer Drug Delivery

被引:85
|
作者
Shen, Youqing [1 ]
Zhan, Yihong [1 ]
Tang, Jianbin [1 ]
Xu, Peisheng [1 ]
Johnson, Patrick A. [1 ]
Radosz, Maciej [1 ]
Van Kirk, Edward A. [2 ]
Murdoch, William J. [2 ]
机构
[1] Univ Wyoming, Soft Mat Lab, Dept Chem & Petr Engn, Laramie, WY 82071 USA
[2] Univ Wyoming, Dept Anim Sci, Laramie, WY 82071 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
nanoparticles; pH-sensitive; self-assembly; polymer brush; drug delivery;
D O I
10.1002/aic.11600
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
polymer nanoparticles are extensively explored as drug carriers but they generally have issues of premature burst drug release. slow cellular uptake, and retention in acidic intracellular Compartments. Herein, we report multifunctioning three-layered nanoparticles (3LNPs) that can overcome these problems. The 3LNPs have a poly(epsilon-caprolactone) (PCL) core, a pH-responsive poly[2-(N,N-diethylamino)ethyl methacrylate] (P-DEA) middle layer and a polyethylene glycol (PEG) outer layer. The pH-responsive PDEA layer is insoluble at pH above 7 but becomes positively charged and soluble via protonation on at pH lower than 6.5. Thus, this layer has three functions: it covers on the PCL core inhibiting the premature burst drug release at the physiological pH, becomes positively charged and thus promotes endocytosis for fast cellular internalization in the acidic interstitium of solid tumors, and is highly positively charged in lysosomes to disrupt the lysosomal membrane and release the nanoparticle into the cytosol. The multifunctioning nanoparticles are an efficient carrier for cancer cytosolic drug delivery. (C) 2008 American Institute of Chemical Engineers AIChE J, 54: 2979-2989, 2008
引用
收藏
页码:2979 / 2989
页数:11
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