pH-Sensitive nanocargo based on smart polymer functionalized graphene oxide for site-specific drug delivery

被引:0
|
作者
Kavitha, Thangavelu [1 ]
Abdi, Syed Izhar Haider [2 ]
Park, Soo-Young [1 ]
机构
[1] Kyungpook Natl Univ, Dept Polymer Sci & Engn, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Biomed Res Inst, Sch Med, Taegu 702701, South Korea
基金
新加坡国家研究基金会;
关键词
WALLED CARBON NANOTUBES; EXFOLIATED GRAPHITE OXIDE; CONTROLLED-RELEASE; TARGETED DELIVERY; WATER; CELLS; NANOCOMPOSITES; NANOPARTICLES; NANOSHEETS; COMPOSITE;
D O I
10.1039/c3cp00008g
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
Graphene oxide (GO) was functionalized covalently with pH-sensitive poly(2-(diethylamino) ethyl methacrylate) (PDEA) by surface-initiated in situ atom transfer radical polymerization. The structure of the PDEA-grafted GO (GO-PDEA) were examined by Fourier-transform infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis and atomic force microscopy. The grafted PDEA endowed the GO sheets with good solubility and stability in physiological solutions. Simple physisorption by p-p stacking and hydrophobic interactions on GO-PDEA can be used to load camptothecin (CPT), a widely used water-insoluble cancer drug. The loaded CPT was released only at the lower (acidic) pH normally found in a tumor environment but not in basic and neutral pH. GO-PDEA did not show practical toxicity to N2a cancer cells but the GO-PDEA-CPT complex exhibited high potency in killing N2a cancer cells in vitro. These results suggest that the GO-PDEA nanocargo carrier might be a promising material for site-specific anticancer drug delivery and controlled release.
引用
收藏
页码:5176 / 5185
页数:10
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