Development of Multifunctional Hyaluronan-Coated Nanoparticles for Imaging and Drug Delivery to Cancer Cells

被引:109
作者
El-Dakdouki, Mohammad H. [1 ]
Zhu, David C. [2 ,3 ,5 ]
El-Boubbou, Kheireddine [1 ]
Kamat, Medha [1 ]
Chen, Jianjun [4 ]
Li, Wei [4 ]
Huang, Xuefei [1 ,5 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Radiol, E Lansing, MI 48824 USA
[3] Michigan State Univ, Dept Psychol, E Lansing, MI 48824 USA
[4] Univ Tennessee, Hlth Sci Ctr, Coll Pharm, Memphis, TN 38163 USA
[5] Michigan State Univ, Biomed Imaging Res Ctr, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
IRON-OXIDE NANOPARTICLES; MAGNETIC GLYCO-NANOPARTICLES; MULTIDRUG-RESISTANCE; IN-VITRO; ANTITUMOR-ACTIVITY; DOXORUBICIN; CD44; DERIVATIVES; COPOLYMER; BINDING;
D O I
10.1021/bm300046h
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Currently, there is high interest in developing multifunctional theranostic platforms for cancer monitoring and chemotherapy. Herein, we report hyaluronan (HA)-coated superparamagnetic iron oxide nanoparticles (HA-SPION) as a promising system for targeted imaging and drug delivery. When incubated with cancer cells, HA-SPIONs were rapidly taken up and the internalization of HA-SPION by cancer cells was much higher than the NPs without HA coating. The high magnetic relaxivity of HA-SPION coupled with enhanced uptake enabled magnetic resonance imaging of cancer cells. Furthermore, doxorubicin (DOX) was attached onto the nanoparticles through an acid responsive linker. While HA-SPION was not toxic to cells, DOX-HA-SPION was much more potent than free DOX to kill not only drug-sensitive but also multi-drug-resistant cancer cells. This was attributed to differential uptake mechanisms and cellular distributions of free DOX and DOX-HA-SPION in cancer cells.
引用
收藏
页码:1144 / 1151
页数:8
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